Rx0000018 |
ACADIA Pharmaceuticals Inc. |
12/31/2019 |
63090034030 |
NUPLAZID Oral Capsule 34 MG 30 |
12/30/2019 |
155.00 |
3341.00 |
08/27/2038 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which ACADIA believes is otherwise in the public domain or publicly available. (2) For the latest the latest patent expiration, please refer to Approved Drug Products with Therapeutic Equivalence Evaluations (the “Orange Book”). (3) This drug was developed by ACADIA , therefore the following fields related to drug acquisition have been left blank: ACQUISITION_DATE, ACQUIRED_FROM_COMPANY, ACQUISITION_PRICE, ACQUISITION_PRICE_NONPUBLIC, ACQUISITION_PRICE_COMMENT, WAC_AT_ACQUISITION, YEAR_INTRODUCED, WAC_AT_INTRODUCTION. |
Rx0000018 |
ACADIA Pharmaceuticals Inc. |
12/31/2019 |
63090010030 |
NUPLAZID Oral Tablet 10 MG 30 |
12/30/2019 |
155.00 |
3341.00 |
03/23/2037 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which ACADIA believes is otherwise in the public domain or publicly available. (2) For the latest the latest patent expiration, please refer to Approved Drug Products with Therapeutic Equivalence Evaluations (the “Orange Book”). (3) This drug was developed by ACADIA , therefore the following fields related to drug acquisition have been left blank: ACQUISITION_DATE, ACQUIRED_FROM_COMPANY, ACQUISITION_PRICE, ACQUISITION_PRICE_NONPUBLIC, ACQUISITION_PRICE_COMMENT, WAC_AT_ACQUISITION, YEAR_INTRODUCED, WAC_AT_INTRODUCTION. |
Rx0000021 |
Acorda Therapeutics, Inc. |
12/31/2019 |
10144042760 |
AMPYRA (dalfampridine) Extended Release 10mg Tablets / 60 Tablet Bottles |
10/01/2019 |
242.27 |
2934.14 |
None |
Innovator Multiple Source Drug |
98877 |
None |
AMPYRA® has not been reformulated, but AMPYRA® is the manufacturer's primary source of revenue while revenue from a more recently-approved product, INBRIJA™, increases. |
None |
AMPYRA® has not been reformulated, but AMPYRA® is the manufacturer's primary source of revenue while revenue from a more recently-approved product, INBRIJA™, increases. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Regarding the inquiry relating to acquisition and patent:
Regarding Patent & Patent Expiration: Acorda has filed a request with the FDA to delist the AMPYRA® patents from the Orange Book (Approved Drug Products with Therapeutic Equivalents). There are currently multiple generics on the market.
Regarding Acquisition: Acorda did not acquire AMPYRA® within the previous five year period. |
Rx0000157 |
Acrotech Biopharma LLC |
06/30/2019 |
68152010809 |
BELEODAQ® (belinostat)for Injection - 500mg single-dose vial |
04/01/2019 |
28.28 |
1913.58 |
10/27/2027 |
Single Source Drug |
8569 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
1885.30 |
None |
2014 |
1500.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
09/30/2019 |
68152010809 |
BELEODAQ® (belinostat)for Injection - 500mg single-dose vial |
07/15/2019 |
28.70 |
1942.28 |
10/27/2027 |
Single Source Drug |
9394 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
1885.30 |
None |
2014 |
1500.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
12/31/2019 |
68152010809 |
BELEODAQ® (belinostat)for Injection - 500mg single-dose vial |
10/01/2019 |
29.14 |
1971.42 |
10/27/2027 |
Single Source Drug |
8569 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
1885.30 |
1776.30 |
2014 |
1500.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
06/30/2019 |
48818000101 |
FOLOTYN® (pralatrexate injection) 20mg, 20mg/mL, 1ml Vial |
04/01/2019 |
81.64 |
5524.33 |
05/31/2025 |
Single Source Drug |
3948 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
5442.69 |
None |
2009 |
3125.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
09/30/2019 |
48818000101 |
FOLOTYN® (pralatrexate injection) 20mg, 20mg/mL, 1ml Vial |
07/15/2019 |
82.87 |
5607.20 |
05/31/2025 |
Single Source Drug |
4273 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
5442.69 |
None |
2009 |
3125.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
12/31/2019 |
48818000101 |
FOLOTYN® (pralatrexate injection) 20mg, 20mg/mL, 1ml Vial |
10/01/2019 |
106.53 |
5713.73 |
05/31/2025 |
Single Source Drug |
3948 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
5442.69 |
5047.97 |
2009 |
3125.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
06/30/2019 |
48818000102 |
FOLOTYN® (pralatrexate injection) 40mg, 20mg/mL, 2ml Vial |
04/01/2019 |
163.28 |
11048.66 |
05/31/2025 |
Single Source Drug |
2516 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
10885.38 |
None |
2009 |
6250.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
09/30/2019 |
48818000102 |
FOLOTYN® (pralatrexate injection) 40mg, 20mg/mL, 2ml Vial |
07/15/2019 |
165.74 |
11214.40 |
05/31/2025 |
Single Source Drug |
2667 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
10885.38 |
None |
2009 |
6250.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
12/31/2019 |
48818000102 |
FOLOTYN® (pralatrexate injection) 40mg, 20mg/mL, 2ml Vial |
10/01/2019 |
213.06 |
11427.46 |
05/31/2025 |
Single Source Drug |
2516 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
10885.38 |
10095.94 |
2009 |
6250.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
06/30/2019 |
20536032201 |
MARQIBO® (vinCRIStine sulfate LIPOSOME injection) |
04/01/2019 |
214.41 |
14508.62 |
09/25/2020 |
Single Source Drug |
558 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
14294.21 |
None |
2013 |
9750.00 |
None |
None |
Rx0000157 |
Acrotech Biopharma LLC |
12/31/2019 |
20536032201 |
MARQIBO® (vinCRIStine sulfate LIPOSOME injection) |
10/01/2019 |
565.84 |
15074.46 |
09/25/2020 |
Single Source Drug |
558 |
None |
None |
1 |
None |
1 |
03/01/2019 |
Spectrum Pharmaceuticals |
160000000 |
None |
Acrotech Biopharma acquired the product as part of a portofolio deal involving multiple assets for $160M in upfront payments and up to $140M in additional royalties, and its acquisition price was incorporated into that deal’s overall purchase price. |
14294.21 |
13241.25 |
2013 |
9750.00 |
None |
None |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431011001 |
JUXTAPID 10 MG CAPS, bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431012001 |
JUXTAPID 20 MG CAPS, bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431013001 |
JUXTAPID 30 MG CAPS, bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431014001 |
JUXTAPID 40 MG CAPS, bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431010501 |
JUXTAPID 5 MG CAPS - bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431016001 |
JUXTAPID 60 MG CAPS, bottle of 28 capsules |
01/01/2019 |
3678.85 |
40670.85 |
08/19/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The drug was developed by the manufacturer therefore the acquisition related fields are blank. |
Rx0000203 |
Aegerion Pharmaceuticals, Inc. |
03/31/2019 |
76431021001 |
MYALEPT 11.3MG VIAL - 1 vial |
01/01/2019 |
419.06 |
4632.82 |
07/17/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
01/12/2015 |
AstraZeneca |
325000000 |
None |
None |
3493.00 |
None |
2014 |
3493.00 |
None |
The product was introduced to the market before it was acquired by Aegerion Pharmaceuticals which was later acquired by Amryt in 2019. The information provided in this report is the only information available to Amryt. Amryt has no knowledge of the WAC at introduction. Therefore the WAC Aegerion set after acquisition was used - 3493.00 as reported in MediSpan. |
Rx0000151 |
Aerie Pharmaceuticals Inc. |
09/30/2019 |
07072749725 |
Netarsudil ophthalmic solution 0.02%, 2.5mL bottle |
09/23/2019 |
22.46 |
272.07 |
03/14/2034 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Aerie Pharmaceuticals, Inc. developed Rhopressa. It is not an acquired product. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478021515 |
Atropine Sulfate Ophth Sol 1% 10mg/mL,15mL, 1 Bottle |
03/18/2019 |
31.09 |
114.83 |
None |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478030703 |
Azithromycin 1% Opth Soln 10mg, 2.5ml, 1 Bottle |
03/18/2019 |
18.58 |
206.21 |
03/31/2019 |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478050305 |
Dehydrated Alcohol 0.98mL/mL, 5ml, 10 Vials |
03/18/2019 |
261.94 |
1295.00 |
None |
Non-innovator Multiple Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478010610 |
Levofloxacin Ophth Solution 0.5%, 5ml, 1 Bottle/ EA |
03/18/2019 |
52.39 |
114.89 |
None |
Non-innovator Multiple Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478070102 |
lndocyanine Green 25mg,10ml / Amp, 6Amp |
03/18/2019 |
111.23 |
683.59 |
None |
Innovator Multiple Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478060930 |
Tafluprost Ophth Sol .0015%.3ml/.0045mg, .3mL-30 UD pk |
03/18/2019 |
19.19 |
213.01 |
05/28/2029 |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
04/01/2014 |
Merck |
None |
1 |
No comment |
103.79 |
None |
2014 |
103.79 |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
17478004532 |
Tetracaine HCI Injection 1% lOmg/mL, 2ml, 25 Ampules |
03/18/2019 |
994.47 |
1898.53 |
None |
Non-innovator Multiple Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
76478000105 |
Timolol 0.25% Opth Solution 2.56mg/mL, 5ml, 1 Bottle |
03/18/2019 |
11.51 |
127.76 |
None |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
76478000215 |
Timolol 0.5% Opth Solution 5.12mg/ml, 15ml, 1 Bottle |
03/18/2019 |
36.74 |
407.89 |
None |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
76478000205 |
Timolol 0.5% Opth Solution 5.12mg/mL, 5ml, 1 Bottle |
03/18/2019 |
12.71 |
141.07 |
None |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000085 |
Akorn Inc |
03/31/2019 |
76478000210 |
Timolol 0.50% Opth Solution 5.12mg/ml, 10ml, 1 Bottle |
03/18/2019 |
24.41 |
271.01 |
None |
Single Source Drug |
None |
1 |
Cost of improvements in manufacturing process of products. |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Patent Expiration Dates provided for products under patent as of effective date of applicable WAC increase.
Information requested in Columns N-U provided for products acquired within five years of the effective date of applicable WAC increase. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004230 |
Irbesartan 150mg Tablet 30ct |
04/17/2019 |
63.91 |
75.00 |
None |
Non-innovator Multiple Source Drug |
12060 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004271 |
Irbesartan 150mg Tablet 500ct |
04/17/2019 |
1068.80 |
1250.00 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004290 |
Irbesartan 150mg Tablet 90ct |
04/17/2019 |
191.72 |
225.00 |
None |
Non-innovator Multiple Source Drug |
14040 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004330 |
Irbesartan 300mg Tablet 30ct |
04/17/2019 |
76.15 |
90.00 |
None |
Non-innovator Multiple Source Drug |
3828 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004371 |
Irbesartan 300mg Tablet 500ct |
04/17/2019 |
1269.20 |
1500.00 |
None |
Non-innovator Multiple Source Drug |
3984 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004390 |
Irbesartan 300mg Tablet 90ct |
05/01/2019 |
228.46 |
270.00 |
None |
Non-innovator Multiple Source Drug |
23292 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004130 |
Irbesartan 75mg Tablet 30ct |
04/17/2019 |
49.46 |
60.00 |
None |
Non-innovator Multiple Source Drug |
18744 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332004190 |
Irbesartan 75mg Tablet 90ct |
04/17/2019 |
148.38 |
180.00 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332005130 |
Irbesartan/Hydrochlorothiazide 150mg-12.5mg Tablet 30ct |
04/08/2019 |
66.30 |
90.00 |
None |
Non-innovator Multiple Source Drug |
48 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332005190 |
Irbesartan/Hydrochlorothiazide 150mg-12.5mg Tablet 90ct |
04/08/2019 |
201.30 |
270.00 |
None |
Non-innovator Multiple Source Drug |
936 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332005230 |
Irbesartan/Hydrochlorothiazide 300mg-12.5mg Tablet 30ct |
04/08/2019 |
51.30 |
97.50 |
None |
Non-innovator Multiple Source Drug |
10356 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
06/30/2019 |
62332005290 |
Irbesartan/Hydrochlorothiazide 300mg-12.5mg Tablet 90ct |
04/08/2019 |
157.20 |
292.50 |
None |
Non-innovator Multiple Source Drug |
1860 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
09/30/2019 |
62332004930 |
Losartan Potassium/Hydrochlorothiazide 100mg-12.5mg Tablet 30ct |
07/15/2019 |
36.03 |
41.25 |
None |
Non-innovator Multiple Source Drug |
6732 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
09/30/2019 |
62332004990 |
Losartan Potassium/Hydrochlorothiazide 100mg-12.5mg Tablet 90ct |
07/15/2019 |
110.47 |
123.75 |
None |
Non-innovator Multiple Source Drug |
2028 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
09/30/2019 |
62332005030 |
Losartan Potassium/Hydrochlorothiazide 100mg-25mg Tablet 30ct |
07/15/2019 |
36.03 |
41.25 |
None |
Non-innovator Multiple Source Drug |
17784 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000235 |
Alembic Pharmaceuticals, Inc. |
09/30/2019 |
62332005090 |
Losartan Potassium/Hydrochlorothiazide 100mg-25mg Tablet 90ct |
07/15/2019 |
110.35 |
123.75 |
None |
Non-innovator Multiple Source Drug |
3456 |
None |
1. Additional costs of manufacturing and production incurred by its parent Alembic Pharmaceutical, Ltd. Including a) additional cost of key starting materials used to manufacture active ingredients driven by lack of supply from China; b)costs to change Alembic Pharmaceutical, Ltd.’s manufacturing process to eliminate use of recovered solvents in manufacturing; c) additional capital investment for manufacturing of these Sartan products of approximately $200,000 to $300,000 per year; and d) longer and more stringent quality testing requirements mandated by FDA for Sartan products.
2. Any financial penalties and charges to Alembic Sales associated with a WAC price increase.
3. WAC Price of competing products. |
None |
High volume of requests received from customers to supply these products as quickly as possible. Prior to this increased volume of customer requests, Alembic Sales’ revenue and volume for all of these products was very small, driven by poor economics, and its goal was to provide sustainable supply to the market to meet the increased demand. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product was not acquired. This is Alembic ANDA. |
Rx0000039 |
Alkermes, Inc |
03/31/2019 |
65757040103 |
ARISTADA 441 mg/ 1.6mL extended-release injectable suspension |
02/22/2019 |
73.28 |
1294.73 |
10/26/2030 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Aristada was developed in-house |
Rx0000039 |
Alkermes, Inc |
03/31/2019 |
65757040203 |
ARISTADA 662 mg/2.4mL extended-release injectable suspension |
02/22/2019 |
110.01 |
1943.56 |
10/26/2030 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Aristada was developed in-house |
Rx0000039 |
Alkermes, Inc |
03/31/2019 |
65757040303 |
ARISTADA 882 mg/3.2mL extended-release injectable suspension |
02/22/2019 |
146.57 |
2589.46 |
10/26/2030 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Aristada was developed in-house |
Rx0000020 |
Allergan |
03/31/2019 |
00430047801 |
ACTONEL-150 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
17.25 |
369.33 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430047802 |
ACTONEL-150 mg-3-CAPSULE,DELAYED RELEASE |
01/01/2019 |
51.76 |
1108.00 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430047207 |
ACTONEL-35 mg-12-CAPSULE,DELAYED RELEASE |
01/01/2019 |
47.78 |
1022.92 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430047203 |
ACTONEL-35 mg-4-CAPSULE,DELAYED RELEASE |
01/01/2019 |
15.93 |
340.98 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430047115 |
ACTONEL-5 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
17.08 |
365.56 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023350730 |
ACUVAIL-0.45 %-30-DROPPERETTE, SINGLE-USE DROP DISPENSER |
01/01/2019 |
14.87 |
318.31 |
03/07/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023932110 |
ALPHAGAN P-0.1 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
27.74 |
319.78 |
01/10/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023932115 |
ALPHAGAN P-0.1 %-15-CAPSULE,DELAYED RELEASE |
01/01/2019 |
41.62 |
479.74 |
01/10/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023932105 |
ALPHAGAN P-0.1 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
13.88 |
159.96 |
01/10/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023917710 |
ALPHAGAN P-0.15 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.58 |
340.99 |
01/28/2022 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023917715 |
ALPHAGAN P-0.15 %-15-CAPSULE,DELAYED RELEASE |
01/01/2019 |
44.38 |
511.53 |
01/28/2022 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023917705 |
ALPHAGAN P-0.15 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
14.80 |
170.54 |
01/28/2022 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544007660 |
ANDRODERM-2 mg/24 hour-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
53.43 |
615.90 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023599060 |
ANDRODERM-2 mg/24 hour-60-PATCH, TRANSDERMAL 24 HOURS |
01/01/2019 |
53.43 |
615.90 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544007730 |
ANDRODERM-4 mg/24 hour-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
53.43 |
615.90 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023599230 |
ANDRODERM-4 mg/24 hour-30-PATCH, TRANSDERMAL 24 HOURS |
01/01/2019 |
53.43 |
615.90 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456046101 |
ARMOUR THYROID-120 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
13.33 |
153.62 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456045701 |
ARMOUR THYROID-15 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
5.57 |
64.24 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456045801 |
ARMOUR THYROID-30 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
6.54 |
75.42 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456045901 |
ARMOUR THYROID-60 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
7.27 |
83.79 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456046001 |
ARMOUR THYROID-90 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
11.39 |
131.27 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430078327 |
ASACOL HD-800 mg-180-CAPSULE,DELAYED RELEASE |
01/01/2019 |
146.84 |
1692.50 |
11/15/2021 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023590118 |
ASACOL HD-800 mg-180-TABLET, DELAYED RELEASE (ENTERIC COATED) |
01/01/2019 |
146.84 |
1692.50 |
11/15/2021 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430097903 |
ATELVIA-35 mg-4-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.45 |
266.56 |
01/09/2028 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456270001 |
AVYCAZ-2.5 gram-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
31.13 |
358.81 |
06/15/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456270010 |
AVYCAZ-2.5 gram-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
311.30 |
3588.09 |
06/15/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914008052 |
BENTYL-10 mg/mL-2-CAPSULE,DELAYED RELEASE |
01/01/2019 |
19.63 |
420.29 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023031304 |
BLEPHAMIDE S.O.P.-10 %-0.2 %-3.5-OINTMENT (GRAM) |
01/01/2019 |
6.80 |
145.49 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980002210 |
BLEPHAMIDE-10 %-0.2 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
13.59 |
290.98 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980002205 |
BLEPHAMIDE-10 %-0.2 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
6.80 |
145.49 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456141030 |
BYSTOLIC-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.43 |
143.24 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456141090 |
BYSTOLIC-10 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
37.28 |
429.71 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456140263 |
BYSTOLIC-2.5 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
42.21 |
486.53 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456140230 |
BYSTOLIC-2.5 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.43 |
143.24 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456142030 |
BYSTOLIC-20 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.43 |
143.24 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456142090 |
BYSTOLIC-20 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
37.28 |
429.71 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456140563 |
BYSTOLIC-5 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
42.21 |
486.53 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456140530 |
BYSTOLIC-5 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.43 |
143.24 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456140590 |
BYSTOLIC-5 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
37.28 |
429.71 |
12/17/2021 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914050156 |
CANASA-1,000 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
100.79 |
1161.78 |
06/06/2028 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914050142 |
CANASA-1,000 mg-42-CAPSULE,DELAYED RELEASE |
01/01/2019 |
141.11 |
1626.51 |
06/06/2028 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914017014 |
CARAFATE-1 gram/10 mL-420-CAPSULE,DELAYED RELEASE |
01/01/2019 |
18.16 |
209.28 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914017110 |
CARAFATE-1 gram-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
33.71 |
388.51 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456401001 |
CELEXA-10 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
42.40 |
907.71 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456402001 |
CELEXA-20 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
44.19 |
946.10 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456404001 |
CELEXA-40 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
46.12 |
987.29 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023921110 |
COMBIGAN-0.2 %-0.5 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
30.60 |
352.68 |
04/19/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023921115 |
COMBIGAN-0.2 %-0.5 %-15-CAPSULE,DELAYED RELEASE |
01/01/2019 |
45.89 |
528.98 |
04/19/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023921105 |
COMBIGAN-0.2 %-0.5 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
15.30 |
176.33 |
04/19/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611803 |
CONDYLOX-0.5 %-3.5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.58 |
633.34 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544025524 |
CRINONE-4 %-1.125-CAPSULE,DELAYED RELEASE |
01/01/2019 |
5.02 |
107.52 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023615108 |
CRINONE-8 %-1.125-CAPSULE,DELAYED RELEASE |
01/01/2019 |
20.94 |
448.20 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544025612 |
CRINONE-8 %-1.125-CAPSULE,DELAYED RELEASE |
01/01/2019 |
20.94 |
448.20 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023585318 |
DELZICOL-400 mg-180-CAPSULE (WITH DELAYED RELEASE TABLETS) |
01/01/2019 |
60.58 |
698.31 |
04/13/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430375414 |
ESTRACE-0.01 %-42.5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.91 |
344.78 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430072024 |
ESTRACE-0.5 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
25.46 |
545.10 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430072124 |
ESTRACE-1 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
25.46 |
545.10 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430072224 |
ESTRACE-2 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
32.68 |
699.69 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456221230 |
FETZIMA-120 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
34.08 |
392.80 |
05/23/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456220228 |
FETZIMA-20 mg (2)-40 mg (26)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
31.81 |
366.62 |
05/23/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456222030 |
FETZIMA-20 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
34.08 |
392.80 |
05/23/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456224030 |
FETZIMA-40 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
34.08 |
392.80 |
05/23/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456228030 |
FETZIMA-80 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
34.08 |
392.80 |
05/23/2032 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544095601 |
FIORINAL WITH CODEINE #3-30 mg-50 mg-325 mg-40 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
52.97 |
1133.91 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544095501 |
FIORINAL-50 mg-325 mg-40 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
25.27 |
541.03 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980022810 |
FML FORTE-0.25 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
14.27 |
305.53 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980022805 |
FML FORTE-0.25 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
7.14 |
152.76 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023031604 |
FML S.O.P.-0.1 %-3.5-OINTMENT (GRAM) |
01/01/2019 |
7.14 |
152.76 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980021110 |
FML-0.1 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
14.27 |
305.53 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980021105 |
FML-0.1 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
7.14 |
152.76 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544008430 |
GELNIQUE-10 % (100 mg/gram)-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
18.48 |
395.53 |
03/26/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023586111 |
GELNIQUE-10 % (100 mg/gram)-1-GEL IN PACKET (GRAM) |
01/01/2019 |
18.48 |
395.53 |
03/26/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023581230 |
GELNIQUE-100 mg/gram per actuation (10 %)-30-GEL IN METERED-DOSE PUMP |
01/01/2019 |
18.48 |
395.53 |
03/26/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544020431 |
GENERESS FE-0.8 mg-25 mcg (24)/75 mg (~24.7 mg iron)(4)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
22.93 |
490.85 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023429003 |
LASTACAFT-0.25 %-3-DROPS |
01/01/2019 |
10.53 |
225.39 |
12/23/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456201001 |
LEXAPRO-10 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
99.54 |
1147.35 |
02/12/2023 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456202001 |
LEXAPRO-20 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
103.87 |
1197.27 |
02/12/2023 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456200501 |
LEXAPRO-5 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
95.21 |
1097.38 |
02/12/2023 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544003554 |
LILETTA-19.5 mcg/24 hour (5 years) 52 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
65.02 |
749.40 |
03/22/2034 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023585801 |
LILETTA-19.5 mcg/24 hour (5 years) 52 mg-1-INTRAUTERINE DEVICE |
01/01/2019 |
65.02 |
749.40 |
03/22/2034 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456120130 |
LINZESS-145 mcg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
36.77 |
423.83 |
08/16/2033 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456120230 |
LINZESS-290 mcg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
36.77 |
423.83 |
08/16/2033 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456120330 |
LINZESS-72 mcg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
36.77 |
423.83 |
08/16/2033 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430042014 |
LO LOESTRIN FE-1 mg-10 mcg (24)/10 mcg (2)/75 mg (2)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
61.04 |
703.59 |
02/02/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023320503 |
LUMIGAN-0.01 %-2.5-DROPS |
01/01/2019 |
17.09 |
196.97 |
03/16/2025 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023320505 |
LUMIGAN-0.01 %-5-DROPS |
01/01/2019 |
34.16 |
393.78 |
03/16/2025 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023320508 |
LUMIGAN-0.01 %-7.5-DROPS |
01/01/2019 |
51.24 |
590.64 |
03/16/2025 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430054050 |
MINASTRIN 24 FE-1 mg-20 mcg (24)/75 mg (4)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
41.49 |
888.13 |
04/06/2019 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456430001 |
MONUROL-3 gram-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
7.54 |
86.92 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456341433 |
NAMENDA XR-14 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.32 |
464.77 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456341490 |
NAMENDA XR-14 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
120.97 |
1394.32 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456342133 |
NAMENDA XR-21 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.32 |
464.77 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456342833 |
NAMENDA XR-28 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.32 |
464.77 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456342890 |
NAMENDA XR-28 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
120.97 |
1394.32 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456340029 |
NAMENDA XR-7 mg (7)-14 mg (7)-21 mg (7)-28 mg (7)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
37.64 |
433.80 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456340733 |
NAMENDA XR-7 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.32 |
464.77 |
09/24/2029 |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456121430 |
NAMZARIC-14 mg-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.14 |
462.66 |
12/05/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456122130 |
NAMZARIC-21 mg-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.14 |
462.66 |
12/05/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456122830 |
NAMZARIC-28 mg-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.14 |
462.66 |
12/05/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456122929 |
NAMZARIC-7 mg-10 mg (7)/14 mg-10 mg (7)/21 mg-10 mg(7)/28 mg-10 mg(7)-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
37.46 |
431.81 |
12/05/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456120730 |
NAMZARIC-7 mg-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
40.14 |
462.66 |
12/05/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023615301 |
OXYTROL-3.9 mg/24 hour-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
3.97 |
84.98 |
04/26/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544092054 |
OXYTROL-3.9 mg/24 hour-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
3.97 |
84.98 |
04/26/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023615308 |
OXYTROL-3.9 mg/24 hour-8-CAPSULE,DELAYED RELEASE |
01/01/2019 |
31.76 |
679.85 |
04/26/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544092008 |
OXYTROL-3.9 mg/24 hour-8-CAPSULE,DELAYED RELEASE |
01/01/2019 |
31.76 |
679.85 |
04/26/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980018010 |
PRED FORTE-1 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
13.59 |
290.98 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980018015 |
PRED FORTE-1 %-15-CAPSULE,DELAYED RELEASE |
01/01/2019 |
20.39 |
436.47 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980018005 |
PRED FORTE-1 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
6.80 |
145.49 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980017410 |
PRED MILD-0.12 %-10-CAPSULE,DELAYED RELEASE |
01/01/2019 |
13.59 |
290.98 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
11980017405 |
PRED MILD-0.12 %-5-CAPSULE,DELAYED RELEASE |
01/01/2019 |
6.80 |
145.49 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023006604 |
PRED-G-0.3 %-0.6 %-3.5-OINTMENT (GRAM) |
01/01/2019 |
6.80 |
145.49 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023010605 |
PRED-G-0.3 %-1 %-5-SUSPENSION, DROPS(FINAL DOSAGE FORM)(ML) |
01/01/2019 |
6.80 |
145.49 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914060120 |
PYLERA-140 mg-125 mg-125 mg-120-CAPSULE,DELAYED RELEASE |
01/01/2019 |
43.05 |
921.54 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023614730 |
RAPAFLO-4 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.21 |
261.48 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544015130 |
RAPAFLO-4 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.21 |
261.48 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023614230 |
RAPAFLO-8 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.21 |
261.48 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544015230 |
RAPAFLO-8 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
12.21 |
261.48 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023614290 |
RAPAFLO-8 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
36.64 |
784.40 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
52544015219 |
RAPAFLO-8 mg-90-CAPSULE,DELAYED RELEASE |
01/01/2019 |
36.64 |
784.40 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914030180 |
RECTIV-0.4 % (w/w)-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.93 |
640.74 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023530105 |
RESTASIS MULTIDOSE-0.05 %-5.5-DROPS |
01/01/2019 |
48.39 |
557.72 |
05/11/2034 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023916330 |
RESTASIS-0.05 %-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
24.19 |
278.85 |
08/27/2024 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023916360 |
RESTASIS-0.05 %-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
48.39 |
557.72 |
08/27/2024 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430021014 |
SARAFEM-10 mg-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
27.31 |
584.74 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00430022014 |
SARAFEM-20 mg-28-CAPSULE,DELAYED RELEASE |
01/01/2019 |
27.31 |
584.74 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456151060 |
SAVELLA-100 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
33.14 |
381.93 |
09/19/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456150055 |
SAVELLA-12.5 mg (5)-25 mg (8)-50 mg (42)-55-CAPSULE,DELAYED RELEASE |
01/01/2019 |
30.37 |
350.10 |
09/19/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456151260 |
SAVELLA-12.5 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
33.14 |
381.93 |
09/19/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456152560 |
SAVELLA-25 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
33.14 |
381.93 |
09/19/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456155060 |
SAVELLA-50 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
33.14 |
381.93 |
09/19/2029 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023586230 |
TAYTULLA-1 mg-20 mcg (24)/75 mg (4)-28-CAPSULE |
01/01/2019 |
81.10 |
934.74 |
03/29/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456040001 |
TEFLARO-400 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
16.67 |
192.12 |
02/10/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456040010 |
TEFLARO-400 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
166.68 |
1921.21 |
02/10/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456060001 |
TEFLARO-600 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
16.67 |
192.12 |
02/10/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456060010 |
TEFLARO-600 mg-1-CAPSULE,DELAYED RELEASE |
01/01/2019 |
166.68 |
1921.21 |
02/10/2031 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914079010 |
URSO FORTE-500 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
45.59 |
975.95 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
58914078510 |
URSO-250 mg-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
25.73 |
550.74 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
61874010060 |
VIBERZI-100 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
108.85 |
1254.66 |
03/25/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
61874007560 |
VIBERZI-75 mg-60-CAPSULE,DELAYED RELEASE |
01/01/2019 |
108.85 |
1254.66 |
03/25/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456110130 |
VIIBRYD-10 mg (7)-20 mg (23)-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
23.62 |
272.24 |
06/05/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456111030 |
VIIBRYD-10 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
23.62 |
272.24 |
06/05/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456112030 |
VIIBRYD-20 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
23.62 |
272.24 |
06/05/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00456114030 |
VIIBRYD-40 mg-30-CAPSULE,DELAYED RELEASE |
01/01/2019 |
23.62 |
272.24 |
06/05/2022 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611001 |
ZENPEP-10,000 unit-32,000 unit-42,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.07 |
335.02 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030602 |
ZENPEP-10,000 unit-34,000 unit-55,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
29.07 |
335.02 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611101 |
ZENPEP-15,000 unit-47,000 unit-63,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
41.98 |
483.87 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030202 |
ZENPEP-15,000 unit-51,000 unit-82,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
41.98 |
483.87 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611201 |
ZENPEP-20,000 unit-63,000 unit-84,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
57.02 |
657.27 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030302 |
ZENPEP-20,000 unit-68,000 unit-109,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
57.02 |
657.27 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611601 |
ZENPEP-25,000 unit-79,000 unit-105,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
70.56 |
813.34 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030502 |
ZENPEP-25,000 unit-85,000 unit-136,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
70.56 |
813.34 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611301 |
ZENPEP-3,000 unit-10,000 unit-14,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
15.41 |
177.63 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030402 |
ZENPEP-3,000 unit-10,000 unit-16,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
15.41 |
177.63 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611401 |
ZENPEP-40,000 unit-126,000 unit-168,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
112.54 |
1297.15 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030702 |
ZENPEP-40,000 unit-136,000 unit-218,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
112.54 |
1297.15 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
00023611501 |
ZENPEP-5,000 unit-17,000 unit-24,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
14.70 |
169.48 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000020 |
Allergan |
03/31/2019 |
42865030002 |
ZENPEP-5,000 unit-17,000 unit-27,000 unit-100-CAPSULE,DELAYED RELEASE |
01/01/2019 |
14.70 |
169.48 |
02/20/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
All products have been owned or launched by Allergan in the past 5 years inclusive of Actavis and Allergan who merged in 2015 |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
03/31/2019 |
59338077501 |
ferumoxytol 510MG/17 mL Feraheme 510mg Each |
01/01/2019 |
27.46 |
942.79 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
06/30/2019 |
59338077501 |
ferumoxytol 510MG/17 mL Feraheme 510mg Each |
04/01/2019 |
28.28 |
971.07 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
09/30/2019 |
59338077501 |
ferumoxytol 510MG/17 mL Feraheme 510mg Each |
07/01/2019 |
29.13 |
1000.20 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting.
As a part of our business model at AMAG Pharmaceuticals, we perform additional research to monitor safety, understand real life experiences, and develop better delivery mechanisms, dosage, and improved product formulations. We may also conduct additional clinical trials to expand product labels in the same therapeutic area or in a new indications. Often the investment in such endeavors is spread over many years and cannot be captured in a single change in WAC. As a result of these efforts, AMAG received FDA approval for an expanded label for Feraheme in February 2018 to allow treatment of all eligible adults with iron deficiency anemia. This sNDA approval doubles the number of patients who could benefit from Feraheme to include both CKD and non-CKD patients |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
12/31/2019 |
59338077501 |
ferumoxytol 510MG/17 mL Feraheme 510mg Each |
10/01/2019 |
30.01 |
1030.21 |
06/30/2023 |
Single Source Drug |
None |
1 |
Pricing is a complex construct which requires a broad analysis of many factors across the organization. Changes in our WAC, or list price, for a product may not be solely dependent on or determined by the factors related to the product impacted by the price increase.
As a part of our business model at AMAG Pharmaceuticals, we perform additional research to monitor safety, understand real life experiences, and develop better delivery mechanisms, dosage, and improved product formulations. We may also conduct additional clinical trials to expand product labels in the same therapeutic area or in a new indications. Often the investment in such endeavors is spread over many years and cannot be captured in a single change in WAC. For example, as a result of these types of activities, we received FDA approval for an expanded label for Feraheme in early 2018 to allow treatment of all eligible adults with iron deficiency anemia.
The distribution of patients across Commercial and Government insurers and the reimbursement landscape for prescribers are constantly changing and must be taken into consideration to the extent they are known or can be anticipated. Pricing decisions may include current trends and anticipated changes in the discounts, service fees, and rebates that are paid to insurers, group purchasing organizations, pharmacy benefit managers, government agencies, hospitals, physicians, wholesalers, pharmacies and other third parties to ensure that patients are able to have broad access and receive appropriate levels of care and support in connection with our products.
Finally, a key consideration in determining a WAC change for Feraheme is based on the fact that Medicare Average Sales Price (ASP) is the primary reimbursement basis for most prescribers of Feraheme. Our strategy is to maintain a stable ASP for Feraheme, as this is critical to ensure continued broad access for patients. The reported ASP changes on a quarterly basis and is impacted by many of the factors identified above relating to the level of discounts and fees paid, as well as demand and forecasted inventory. |
None |
This WAC increase is not necessitated by a change or improvement in the prescription drug. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
03/31/2019 |
59338077510 |
ferumoxytol 510MG/17 mL Feraheme 510mg/17 mL CTN/10 |
01/01/2019 |
274.60 |
9427.90 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
06/30/2019 |
59338077510 |
ferumoxytol 510MG/17 mL Feraheme 510mg/17 mL CTN/10 |
04/01/2019 |
282.80 |
9710.70 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
09/30/2019 |
59338077510 |
ferumoxytol 510MG/17 mL Feraheme 510mg/17 mL CTN/10 |
07/01/2019 |
291.32 |
10002.02 |
06/30/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting.
As a part of our business model at AMAG Pharmaceuticals, we perform additional research to monitor safety, understand real life experiences, and develop better delivery mechanisms, dosage, and improved product formulations. We may also conduct additional clinical trials to expand product labels in the same therapeutic area or in a new indications. Often the investment in such endeavors is spread over many years and cannot be captured in a single change in WAC. As a result of these efforts, AMAG received FDA approval for an expanded label for Feraheme in February 2018 to allow treatment of all eligible adults with iron deficiency anemia. This sNDA approval doubles the number of patients who could benefit from Feraheme to include both CKD and non-CKD patients |
Rx0000037 |
AMAG Pharmaceuticals, Inc. |
12/31/2019 |
59338077510 |
ferumoxytol 510MG/17 mL Feraheme 510mg/17 mL CTN/10 |
10/01/2019 |
300.06 |
10302.08 |
06/30/2023 |
Single Source Drug |
None |
1 |
Pricing is a complex construct which requires a broad analysis of many factors across the organization. Changes in our WAC, or list price, for a product may not be solely dependent on or determined by the factors related to the product impacted by the price increase.
As a part of our business model at AMAG Pharmaceuticals, we perform additional research to monitor safety, understand real life experiences, and develop better delivery mechanisms, dosage, and improved product formulations. We may also conduct additional clinical trials to expand product labels in the same therapeutic area or in a new indications. Often the investment in such endeavors is spread over many years and cannot be captured in a single change in WAC. For example, as a result of these types of activities, we received FDA approval for an expanded label for Feraheme in early 2018 to allow treatment of all eligible adults with iron deficiency anemia.
The distribution of patients across Commercial and Government insurers and the reimbursement landscape for prescribers are constantly changing and must be taken into consideration to the extent they are known or can be anticipated. Pricing decisions may include current trends and anticipated changes in the discounts, service fees, and rebates that are paid to insurers, group purchasing organizations, pharmacy benefit managers, government agencies, hospitals, physicians, wholesalers, pharmacies and other third parties to ensure that patients are able to have broad access and receive appropriate levels of care and support in connection with our products.
Finally, a key consideration in determining a WAC change for Feraheme is based on the fact that Medicare Average Sales Price (ASP) is the primary reimbursement basis for most prescribers of Feraheme. Our strategy is to maintain a stable ASP for Feraheme, as this is critical to ensure continued broad access for patients. The reported ASP changes on a quarterly basis and is impacted by many of the factors identified above relating to the level of discounts and fees paid, as well as demand and forecasted inventory. |
None |
This WAC increase is not necessitated by a change or improvement in the prescription drug. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Feraheme was developed by AMAG and not subject to acquisition reporting |
Rx0000050 |
Amarin Pharma, Inc. |
12/31/2019 |
52937000120 |
Vascepa(Icosapent ethyl) 120 1g |
12/31/2019 |
27.33 |
330.98 |
06/28/2033 |
Single Source Drug |
3158163 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
https://reports.siera.oshpd.ca.gov/api/report/drug-pricing/attachment?id=336 |
VASCEPA is an ethyl ester of eicosapentaenoic acid (EPA)
indicated as an adjunct to diet to reduce triglyceride (TG)
levels, developed, and manufactured by Amarin Pharmaceuticals. |
Rx0000050 |
Amarin Pharma, Inc. |
12/31/2019 |
52937000340 |
Vascepa(Icosapent ethyl) 240 500 mg |
12/31/2019 |
31.97 |
387.24 |
06/28/2033 |
Single Source Drug |
34858 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
https://reports.siera.oshpd.ca.gov/api/report/drug-pricing/attachment?id=337 |
VASCEPA is an ethyl ester of eicosapentaenoic acid (EPA)
indicated as an adjunct to diet to reduce triglyceride (TG)
levels, developed, and manufactured by Amarin Pharmaceuticals. |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084037301 |
Acetaminophen & Codeine Phosphate Tablet CIII 300mg/60mg 100UD |
12/13/2019 |
33.79 |
92.50 |
None |
Non-innovator Multiple Source Drug |
3545 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084077725 |
Acetaminophen ER Tablet 650mg 30UD |
12/05/2019 |
6.45 |
25.13 |
None |
Non-innovator Multiple Source Drug |
3382 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084010701 |
Acyclovir Capsule 200mg 100UD |
12/13/2019 |
4.67 |
34.08 |
None |
Non-innovator Multiple Source Drug |
6413 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
60687028621 |
Bromocriptine Mesylate Tablet 2.5mg 30UD |
03/27/2019 |
59.82 |
206.88 |
None |
Non-innovator Multiple Source Drug |
3081 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084028101 |
Carbidopa & Levodopa ER Tablet 25mg/100mg 100UD |
12/05/2019 |
47.29 |
78.44 |
None |
Non-innovator Multiple Source Drug |
8151 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084024401 |
Clindamycin HCl Capsule 300mg 100UD |
08/01/2019 |
19.71 |
110.58 |
None |
Non-innovator Multiple Source Drug |
4662 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
60687042321 |
Clobazam Tablet CIV 10mg 30UD |
12/05/2019 |
11.25 |
65.00 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
60687035825 |
Colchicine Capsule 0.6mg 30UD |
11/08/2019 |
37.12 |
204.00 |
None |
Non-innovator Multiple Source Drug |
3321 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084060621 |
Desmopressin Acetate Tablet 0.1mg 30UD |
11/08/2019 |
13.06 |
56.98 |
None |
Non-innovator Multiple Source Drug |
5246 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084033301 |
Diclofenac Sodium DR Tablet 75mg 100UD |
12/05/2019 |
13.55 |
67.05 |
None |
Non-innovator Multiple Source Drug |
1259 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
60687036901 |
Dicyclomine HCl Capsule 10mg 100UD |
09/27/2019 |
9.57 |
54.94 |
None |
Non-innovator Multiple Source Drug |
1743 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
60687022801 |
Diltiazem HCI Capsule ER 24h 300mg 100UD |
09/12/2019 |
29.58 |
158.99 |
None |
Non-innovator Multiple Source Drug |
2204 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084074332 |
Doxycycline Capsule 100mg 20UD |
03/05/2019 |
8.63 |
29.81 |
None |
Non-innovator Multiple Source Drug |
14708 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084032921 |
Fenofibrate Capsule 200mg 30UD |
12/05/2019 |
35.23 |
150.00 |
None |
Non-innovator Multiple Source Drug |
1761 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084028801 |
Fludrocortisone Acetate Tablet 0.1mg 100UD |
03/05/2019 |
14.16 |
84.38 |
None |
Non-innovator Multiple Source Drug |
16476 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084072921 |
Galantamine Tablet 4mg 30UD |
08/01/2019 |
44.47 |
105.00 |
None |
Non-innovator Multiple Source Drug |
1695 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084011201 |
Glipizide ER Tablet 10mg 100UD |
12/05/2019 |
15.50 |
88.44 |
None |
Non-innovator Multiple Source Drug |
2238 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
06/30/2019 |
68084029521 |
Glipizide ER Tablet 2.5mg 30UD |
05/13/2019 |
4.25 |
34.00 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Price increase >16% when factoring previous two years of price changes. The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084074825 |
Guanfacine Tablet 1mg 30UD |
03/05/2019 |
22.21 |
46.90 |
None |
Non-innovator Multiple Source Drug |
8106 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
06/30/2019 |
68084025021 |
Haloperidol Tablet 20mg 30UD |
05/23/2019 |
34.28 |
139.81 |
None |
Non-innovator Multiple Source Drug |
4597 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
06/30/2019 |
60687016101 |
Haloperidol Tablet 5mg 100UD |
05/29/2019 |
26.29 |
91.00 |
None |
Non-innovator Multiple Source Drug |
12693 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084084701 |
Hydroxyzine Pamoate Capsule 25mg 100UD |
09/27/2019 |
25.32 |
50.00 |
None |
Non-innovator Multiple Source Drug |
24756 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68001037400 |
ISOSORBIDE DINITRATE TAB 10MG 100 |
03/28/2019 |
28.89 |
86.68 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Market Conditions |
None |
No change or improvement in the drug product |
None |
02/27/2019 |
Blue Point Laboratories |
350955 |
None |
BluePoint Laboratories and AHP are both owned by AmerisourceBergen - the acquisition price listed is the Q1 total for all units received within Q1 2019. AHP is the US distributor for Bluepoint product. |
57.79 |
None |
2019 |
57.79 |
None |
Bluepoint Laboratories is a sibling company with AHP as its US distributor and is the responsible party for distribution of their products. |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68001037500 |
ISOSORBIDE DINITRATE TAB 20MG 100 |
03/28/2019 |
31.78 |
95.35 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Market Conditions |
None |
No change or improvement in the drug product |
None |
02/27/2019 |
Blue Point Laboratories |
448145 |
None |
BluePoint Laboratories and AHP are both owned by AmerisourceBergen - the acquisition price listed is the Q1 total for all units received within Q1 2019. AHP is the US distributor for Bluepoint product. |
63.57 |
None |
2019 |
63.57 |
None |
Bluepoint Laboratories is a sibling company with AHP as its US distributor and is the responsible party for distribution of their products. |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68001033708 |
LISINOPRIL TAB 40 MG 1000 |
02/11/2019 |
47.30 |
116.36 |
None |
Non-innovator Multiple Source Drug |
22870 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
03/18/2019 |
Blue Point Laboratories |
207786 |
None |
BluePoint Laboratories and AHP are both owned by AmerisourceBergen - the acquisition price listed is the Q1 total for all units received within Q1 2019. AHP is the US distributor for Bluepoint product. |
116.36 |
None |
2017 |
116.36 |
None |
Bluepoint Laboratories is a sibling company with AHP as its US distributor and is the responsible party for distribution of their products. |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68001033308 |
LISINOPRIL TAB 5 MG 1000 |
02/11/2019 |
6.80 |
37.41 |
None |
Non-innovator Multiple Source Drug |
22686 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
03/15/2019 |
Blue Point Laboratories |
245872 |
None |
BluePoint Laboratories and AHP are both owned by AmerisourceBergen - the acquisition price listed is the Q1 total for all units received within Q1 2019. AHP is the US distributor for Bluepoint product. |
30.61 |
None |
2017 |
30.61 |
None |
Bluepoint Laboratories is a sibling company with AHP as its US distributor and is the responsible party for distribution of their products. |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084073801 |
Methadone HCl Tablet CII 10mg 100UD |
12/05/2019 |
4.38 |
30.26 |
None |
Non-innovator Multiple Source Drug |
14073 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
60687035701 |
Methimazole Tablet 5mg 100UD |
09/04/2019 |
13.35 |
50.00 |
None |
Non-innovator Multiple Source Drug |
700 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084067601 |
Metoclopramide Tablet 10mg 100UD |
09/04/2019 |
19.00 |
40.00 |
None |
Non-innovator Multiple Source Drug |
13788 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084004001 |
Misoprostol Tablet 100mcg 100UD |
12/05/2019 |
70.33 |
206.58 |
None |
Non-innovator Multiple Source Drug |
7108 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084004101 |
Misoprostol Tablet 200mcg 100UD |
12/05/2019 |
67.14 |
227.14 |
None |
Non-innovator Multiple Source Drug |
15565 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
60687037401 |
Nabumetone Tablet 500mg 100UD |
02/18/2019 |
39.11 |
105.00 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68001031800 |
NADOLOL TAB 40MG 100 |
03/28/2019 |
103.06 |
320.94 |
None |
Non-innovator Multiple Source Drug |
2062 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
02/04/2019 |
Blue Point Laboratories |
444930 |
None |
BluePoint Laboratories and AHP are both owned by AmerisourceBergen - the acquisition price listed is the Q1 total for all units received within Q1 2019. AHP is the US distributor for Bluepoint product. |
320.94 |
None |
2017 |
320.94 |
None |
Bluepoint Laboratories is a sibling company with AHP as its US distributor and is the responsible party for distribution of their products. |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084059701 |
Nifedipine ER Tablet 30mg 100UD |
03/14/2019 |
47.84 |
149.00 |
None |
Non-innovator Multiple Source Drug |
14896 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084059801 |
Nifedipine ER Tablet 60mg 100UD |
03/14/2019 |
72.83 |
247.25 |
None |
Non-innovator Multiple Source Drug |
5829 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
03/31/2019 |
68084060321 |
Nifedipine ER Tablet 90mg 30UD |
03/14/2019 |
35.69 |
93.63 |
None |
Non-innovator Multiple Source Drug |
8873 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
62584081201 |
Oxazepam Capsule CIV 10mg 100UD |
12/05/2019 |
42.50 |
198.75 |
None |
Non-innovator Multiple Source Drug |
2113 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
62584081301 |
Oxazepam Capsule CIV 15mg 100UD |
12/05/2019 |
37.48 |
218.73 |
None |
Non-innovator Multiple Source Drug |
4681 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
62584081401 |
Oxazepam Capsule CIV 30mg 100UD |
12/05/2019 |
64.18 |
242.80 |
None |
Non-innovator Multiple Source Drug |
1104 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084084501 |
Oxcarbazepine Tablet 150mg 100UD |
09/04/2019 |
21.54 |
53.85 |
None |
Non-innovator Multiple Source Drug |
9550 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084085301 |
Oxcarbazepine Tablet 300mg 100UD |
09/04/2019 |
26.62 |
88.31 |
None |
Non-innovator Multiple Source Drug |
16133 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084086701 |
Oxcarbazepine Tablet 600mg 100UD |
09/04/2019 |
46.61 |
155.07 |
None |
Non-innovator Multiple Source Drug |
6626 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084004601 |
Paroxetine HCl Tablet 30mg 100UD |
12/13/2019 |
14.82 |
94.82 |
None |
Non-innovator Multiple Source Drug |
783 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084063201 |
Potassium Chloride ER Tablet 10mEq K 100UD |
12/05/2019 |
25.71 |
73.21 |
None |
Non-innovator Multiple Source Drug |
21782 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
12/31/2019 |
68084096425 |
Propylthiouracil Tablet 50mg 30UD |
12/05/2019 |
19.00 |
84.00 |
None |
Non-innovator Multiple Source Drug |
4089 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
60687023101 |
Sertraline Tablet 25mg 100UD |
09/04/2019 |
11.23 |
37.43 |
None |
Non-innovator Multiple Source Drug |
20735 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
60687024201 |
Sertraline Tablet 50mg 100UD |
09/04/2019 |
12.52 |
39.19 |
None |
Non-innovator Multiple Source Drug |
91066 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084034401 |
Topiramate Tablet 100mg 100UD |
08/01/2019 |
22.46 |
47.46 |
None |
Non-innovator Multiple Source Drug |
22870 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000231 |
American Health Packaging |
09/30/2019 |
68084034201 |
Topiramate Tablet 25mg 100UD |
08/01/2019 |
12.76 |
29.76 |
None |
Non-innovator Multiple Source Drug |
32279 |
None |
Market Conditions |
None |
No change or improvement in the drug product |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The acquisition fields do not need to be filled out because the drug was not acquired within the previous 5 years. All the fields that are left blank are due to "Not Applicable". |
Rx0000128 |
American Regent |
09/30/2019 |
00517065001 |
Ferric Carboxymaltose 750 MG/15ML Solution 15 ML UD |
07/01/2019 |
31.29 |
1074.25 |
02/15/2028 |
Single Source Drug |
183439 |
None |
American Regent’s US Standards of Business Conduct (available at https://dsi.com/documents/376460/376852/DSI_SOBC.pdf/248ffd7a-3614-e6cc-bf02-4dd99641a79b) reflects that it is committed to pricing its products fairly and appropriately, and acts independently when setting prices, by factoring in costs, market conditions, customer responses, and the state of competition |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Injectafer is not an acquired product. American Regent is the NDA holder of this NDC. |
Rx0000069 |
Amgen |
03/31/2019 |
58406042541 |
''ENBREL 25 mg (1mL) VIAL (EA), 1 pk'' |
01/17/2019 |
37.76 |
646.76 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406042534 |
''ENBREL 25 mg (1mL) VIAL (EA), 4 pk'' |
01/17/2019 |
151.03 |
2587.03 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406045501 |
''ENBREL 25 mg/0.5mL (0.51mL) SYRINGE (mL), 1 pk'' |
01/17/2019 |
37.76 |
646.76 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406045504 |
''ENBREL 25 mg/0.5mL (0.51mL) SYRINGE (mL), 4 pk'' |
01/17/2019 |
151.03 |
2587.03 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406043501 |
''ENBREL 50 mg/mL (0.98mL) SYRINGE (mL), 1 pk'' |
01/17/2019 |
75.52 |
1293.52 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406044501 |
''ENBREL 50 mg/mL (0.98mL) SYRINGE (mL), 1 pk'' |
01/17/2019 |
75.52 |
1293.52 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406043504 |
''ENBREL 50 mg/mL (0.98mL) SYRINGE (mL), 4 pk'' |
01/17/2019 |
302.06 |
5174.06 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
58406044504 |
''ENBREL 50 mg/mL (0.98mL) SYRINGE (mL), 4 pk'' |
01/17/2019 |
302.06 |
5174.06 |
04/24/2029 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
76075010201 |
''KYPROLIS 30 mg (2 mg/mL) VIAL (EA), 1 pk'' |
01/17/2019 |
33.81 |
1160.83 |
12/07/2027 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
76075010101 |
''KYPROLIS 60 mg VIAL (EA), 1 pk'' |
01/17/2019 |
67.62 |
2321.66 |
12/07/2027 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
55513022101 |
''NPLATE 250 mcg (0.5mL) VIAL (EA), 1 pk'' |
01/17/2019 |
54.13 |
1858.58 |
01/19/2022 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Not acquired within the last five years |
Rx0000069 |
Amgen |
03/31/2019 |
55513022201 |
''NPLATE 500 mcg (1.0mL) VIAL (EA), 1 pk'' |
01/17/2019 |
108.26 |
3717.16 |
01/19/2022 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Developed by Amgen |
Rx0000069 |
Amgen |
03/31/2019 |
55513071001 |
''PROLIA 60 mg (1.0mL) SYRINGE (mL), 1 pk'' |
01/17/2019 |
35.51 |
1219.06 |
02/19/2025 |
Single Source Drug |
None |
1 |
"Amgen's sense of overall societal responsibility shapes our pricing decisions, which are guided by four principles of responsible pricing:
Captures the value of the product: We will set prices for our therapies based on their full value, capturing all clinical, humanistic, and economic benefits; Funds continued scientific innovation: Our pricing will support aggressive investment in the discovery of innovative medicines to treat grievous illnesses; Ensures patient access: Our pricing will balance affordability and availability of patient assistance programs to help ensure patient access to our medicines; Reflects market dynamics: We will manage price in response to competition and evolving reimbursement" |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Developed by Amgen |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
53746066901 |
Acebutolol HCl Oral Capsule 200 MG 100 |
02/06/2019 |
40.90 |
65.00 |
None |
Non-innovator Multiple Source Drug |
105216 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
65162066910 |
Acebutolol HCl Oral Capsule 200 MG 100 |
01/25/2019 |
40.90 |
65.00 |
None |
Non-innovator Multiple Source Drug |
11383 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
53746067001 |
Acebutolol HCl Oral Capsule 400 MG 100 |
02/06/2019 |
55.82 |
86.00 |
None |
Innovator Multiple Source Drug |
20151 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
65162067010 |
Acebutolol HCl Oral Capsule 400 MG 100 |
01/25/2019 |
55.82 |
86.00 |
None |
Innovator Multiple Source Drug |
11172 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846020101 |
Activella (estradiol/norethindrone acetate) Tablets 0.5mg/.01mg 1 Dial x 28 tabs |
01/04/2019 |
23.03 |
255.61 |
None |
Innovator Multiple Source Drug |
8952 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846020201 |
Activella (estradiol/norethindrone acetate) Tablets 1.0mg/.05mg 1 Dial x 28 tabs |
01/04/2019 |
25.31 |
280.95 |
None |
Innovator Multiple Source Drug |
7957 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
52054055022 |
Albenza Oral Tablet 200 MG 2Tabs |
01/04/2019 |
43.72 |
485.34 |
None |
Innovator Multiple Source Drug |
316688 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
52054051309 |
Dexedrine Oral Capsule Extended Release 24 Hour 10 MG 90 caps |
01/04/2019 |
190.05 |
2109.72 |
None |
Innovator Multiple Source Drug |
2649 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
52054051409 |
Dexedrine Oral Capsule Extended Release 24 Hour 15 MG 90 caps |
01/04/2019 |
190.05 |
2109.72 |
None |
Innovator Multiple Source Drug |
4223 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
52054051209 |
Dexedrine Oral Capsule Extended Release 24 Hour 5 MG 90 caps |
01/04/2019 |
190.05 |
2109.72 |
None |
Innovator Multiple Source Drug |
515 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
65162071110 |
Guanfacine HCl Oral Tablet 1 MG 100 |
02/06/2019 |
35.60 |
56.00 |
None |
Innovator Multiple Source Drug |
372489 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
65162071310 |
Guanfacine HCl Oral Tablet 2 MG 100 |
02/06/2019 |
58.40 |
87.00 |
None |
Non-innovator Multiple Source Drug |
109752 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
53746046605 |
Ibuprofen Oral Tablet 800 MG 500 |
03/28/2019 |
11.75 |
80.25 |
None |
Non-innovator Multiple Source Drug |
194 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
65162046650 |
Ibuprofen Oral Tablet 800 MG 500 |
03/28/2019 |
11.75 |
80.25 |
None |
Non-innovator Multiple Source Drug |
237540 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846030115 |
Nizatidine Oral Solution 15mg/mL 480 Bottle |
01/04/2019 |
45.65 |
506.78 |
None |
Non-innovator Multiple Source Drug |
7206 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846088201 |
Prandin® (repaglinide tablets) 1mg 100 Tabs |
01/04/2019 |
71.40 |
792.64 |
None |
Non-innovator Multiple Source Drug |
5667 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
05/07/2018 |
Gemini Laboratories, LLC |
None |
None |
Amneal does not have the ability to separate the portion of the total acquisition price allocated to the individual drug products. Total amount was 117000000 |
656.26 |
625.61 |
2013 |
339.25 |
None |
Column 12 Blank - No change to the product |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846088401 |
Prandin® (repaglinide tablets) 2mg 100 Tab |
01/04/2019 |
71.40 |
792.64 |
None |
Non-innovator Multiple Source Drug |
9733 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
05/07/2018 |
Gemini Laboratories, LLC |
None |
None |
Amneal does not have the ability to separate the portion of the total acquisition price allocated to the individual drug products. Total amount was 117000000 |
656.26 |
625.61 |
2013 |
339.25 |
None |
Column 12 Blank - No change to the product |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846050101 |
Pyridium® (phenazopyridine HCL) 100mg 100 Tab |
01/04/2019 |
71.40 |
443.43 |
None |
Non-innovator Multiple Source Drug |
2557 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
60846050201 |
Pyridium® (phenazopyridine HCL) 200mg 100 Tab |
01/04/2019 |
51.36 |
570.13 |
None |
Non-innovator Multiple Source Drug |
3459 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
64896066101 |
Rytary 23.75mg/95mg ER Cap 100ct |
01/04/2019 |
28.88 |
320.56 |
12/26/2028 |
Single Source Drug |
206350 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
64896066201 |
Rytary 36.25mg/145mg ER Cap 100ct |
01/04/2019 |
28.88 |
320.56 |
12/26/2028 |
Single Source Drug |
205662 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
64896066301 |
Rytary 48.75mg/195mg ER Cap 100ct |
01/04/2019 |
28.88 |
320.56 |
12/26/2028 |
Single Source Drug |
233657 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
03/31/2019 |
64896066401 |
Rytary 61.25mg/245mg ER Cap 100ct |
01/04/2019 |
36.28 |
402.79 |
12/26/2028 |
Single Source Drug |
100797 |
None |
Manufacturing costs and market conditions
require increase to remain on market |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Column 12 Blank - No change to the product
Columns 14 -22 Blank - Products were not acquired from another company. |
Rx0000122 |
Amneal Pharmaceuticals |
06/30/2019 |
65162055650 |
Temazepam Oral Capsule 15 MG 500 |
05/08/2019 |
37.30 |
64.30 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Manufacturing costs and market conditions require increase to remain on market |
None |
No change |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product not acquired from another company. No changes were made to the product .This was a relaunch so there was no unit sales volume during this time frame. |
Rx0000122 |
Amneal Pharmaceuticals |
06/30/2019 |
65162055750 |
Temazepam Oral Capsule 30 MG 500 |
05/08/2019 |
42.25 |
76.90 |
None |
Non-innovator Multiple Source Drug |
0 |
1 |
Manufacturing costs and market conditions require increase to remain on market |
None |
No change |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Product not acquired from another company. No changes were made to the product. This was a relaunch so there was no unit sales volume during this time frame. |
Rx0000271 |
Apotex Corp |
06/30/2019 |
60505058204 |
MOXIFLOXACIN HCL OP/SLN 0.5% 3ML |
04/11/2019 |
33.47 |
66.94 |
None |
Non-innovator Multiple Source Drug |
2099287 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000132 |
Arbor Pharmaceuticals, LLC |
12/31/2019 |
53451010301 |
HORIZANT Oral Tablet Extended Release 300 MG, 30 tablets in a bottle |
10/01/2019 |
23.31 |
411.84 |
06/10/2029 |
Single Source Drug |
59056 |
None |
Increases in rate of inflation, continued investment in innvotion, post-marketing regulatory commitments and requiremens, ongoing pharmacovigilance, market conditions and dynamics |
None |
None |
1 |
07/05/2016 |
Xenoport, Inc. |
467000000 |
None |
Price was for both product strengths and additional IP and assets |
330.40 |
280.00 |
2014 |
162.07 |
None |
All information is provided by Arbor to the best of our knowledge at the time of submission. WAC is reported at the package level not the unit level. Arbor provides this report consistent with its understanding and interpretation of California SB 17 Chapter 603 Chapter 9 § 127681 and its provisions. In providing this report, Arbor does not waive any rights that it may have at law or in equity with respect to the applicability, interpretation, or application of California SB 17 Chapter 603 Chapter 9 § 127681 as it may relate to Arbor or any of its affiliates now or in the future. Arbor, on behalf of itself and affiliates, expressly reserves all such rights. Arbor believes that this submission and of all Arbor related information set forth in this submission is confidential and proprietary, commercial or financial information not subject to disclosure, including under the California Public Records Act (Government Code Section 6250 et seq.) and applicable laws pertaining to trade secrets. We request that the confidentiality of this submission and of all Arbor’s related information herein be maintained to the maximum extent permitted by law. When any of this information is requested, whether under the California Public Records Act (Government Code Section 6250 et seq.) or otherwise, we request that Arbor is notified of the request and afforded the opportunity to submit objections to disclosure. |
Rx0000132 |
Arbor Pharmaceuticals, LLC |
12/31/2019 |
53451010101 |
HORIZANT Oral Tablet Extended Release 600 MG, 30 tablets in a bottle |
10/01/2019 |
23.31 |
411.84 |
06/10/2029 |
Single Source Drug |
215303 |
None |
Increases in rate of inflation, continued investment in innvotion, post-marketing regulatory commitments and requiremens, ongoing pharmacovigilance, market conditions and dynamics |
None |
None |
1 |
07/05/2016 |
Xenoport, Inc. |
467000000 |
None |
Price was for both product strengths and additional IP and assets |
330.40 |
280.00 |
2011 |
99.00 |
None |
All information is provided by Arbor to the best of our knowledge at the time of submission. WAC is reported at the package level not the unit level. Pricing for 2011 is based on information that Arbor obtained in conjunction with the acquisition of Horizant based on publicly available information available at the time. That information is no longer available and Arbor is relying on its records from that time in making this submission.
Arbor provides this report consistent with its understanding and interpretation of California SB 17 Chapter 603 Chapter 9 § 127681 and its provisions. In providing this report, Arbor does not waive any rights that it may have at law or in equity with respect to the applicability, interpretation, or application of California SB 17 Chapter 603 Chapter 9 § 127681 as it may relate to Arbor or any of its affiliates now or in the future. Arbor, on behalf of itself and affiliates, expressly reserves all such rights. Arbor believes that this submission and of all Arbor related information set forth in this submission is confidential and proprietary, commercial or financial information not subject to disclosure, including under the California Public Records Act (Government Code Section 6250 et seq.) and applicable laws pertaining to trade secrets. We request that the confidentiality of this submission and of all Arbor’s related information herein be maintained to the maximum extent permitted by law. When any of this information is requested, whether under the California Public Records Act (Government Code Section 6250 et seq.) or otherwise, we request that Arbor is notified of the request and afforded the opportunity to submit objections to disclosure. |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57883040105 |
Keralac Cream, (urea 47%), Cream, 142 g |
12/19/2019 |
40.03 |
693.00 |
None |
Innovator Multiple Source Drug |
4098 |
None |
Raw materials, regulations |
None |
None |
1 |
08/01/2017 |
Mission Pharmacal Company |
None |
1 |
None |
594.15 |
None |
2014 |
395.00 |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893031210 |
MimyX Cream, n/a, Cream, 100 g |
12/19/2019 |
30.00 |
520.00 |
None |
Single Source Drug |
8772 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893031060 |
Nolix Cream, (flurandrenolide 0.05%), Cream, 120 g |
12/19/2019 |
54.82 |
956.00 |
None |
Non-innovator Multiple Source Drug |
2070 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893031112 |
Nolix Lotion, (flurandrenolide 0.05%), Lotion, 120 mL |
12/19/2019 |
42.12 |
729.00 |
None |
Non-innovator Multiple Source Drug |
3342 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57883040210 |
Plexion Cleanser, (sodium sulfacetamide 9.8%, sulfur 4.8%), Cleanser, 285 g |
12/19/2019 |
40.03 |
693.00 |
None |
Innovator Multiple Source Drug |
65946 |
None |
Raw materials, regulations |
None |
None |
1 |
08/01/2017 |
Mission Pharmacal Company |
None |
1 |
None |
594.15 |
None |
2014 |
395.00 |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57883040460 |
Plexion Cleansing Cloths, (sodium sulfacetamide 9.8%, sulfur 4.8%), Cloths, 60 ct. (4 g each) |
12/19/2019 |
42.82 |
752.00 |
None |
Single Source Drug |
5964 |
None |
Raw materials, regulations |
None |
None |
1 |
08/01/2017 |
Mission Pharmacal Company |
None |
1 |
None |
645.30 |
None |
2014 |
395.00 |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57883040302 |
Plexion Cream, (sodium sulfacetamide 9.8%, sulfur 4.8%), Cream, 57 g |
12/19/2019 |
36.33 |
641.00 |
None |
Innovator Multiple Source Drug |
8168 |
None |
Raw materials, regulations |
None |
None |
1 |
08/01/2017 |
Mission Pharmacal Company |
None |
1 |
None |
550.20 |
None |
2014 |
435.00 |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57883040502 |
Plexion Lotion, (sodium sulfacetamide 9.8%, sulfur 4.8%), Lotion, 57 g |
12/19/2019 |
39.93 |
699.00 |
None |
Innovator Multiple Source Drug |
6918 |
None |
Raw materials, regulations |
None |
None |
1 |
08/01/2017 |
Mission Pharmacal Company |
None |
1 |
None |
599.70 |
None |
2014 |
435.00 |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893030399 |
Riax Foam 5.5%, (benzoyl peroxide 5.5%), Form, 100 g |
12/19/2019 |
30.87 |
543.00 |
None |
Single Source Drug |
4176 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893030499 |
Riax Foam 9.5%, (benzoyl peroxide 9.5%), Form, 100 g |
12/19/2019 |
30.87 |
543.00 |
None |
Single Source Drug |
6246 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893030006 |
SelRx Shampoo, (selenium sulfide 2.3%), Shampoo, 180 mL |
12/19/2019 |
34.72 |
604.00 |
None |
Innovator Multiple Source Drug |
7240 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893030108 |
Utopic Cream, (urea 41%), Cream, 227 g |
12/19/2019 |
49.96 |
883.00 |
None |
Innovator Multiple Source Drug |
7524 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000274 |
Artesa Labs, LLC |
12/31/2019 |
57893030230 |
Vytone Cream, (hydrocortisone acetate 1.9%, iodoquinol 1%), 30 ct. (2 g each) |
12/19/2019 |
48.43 |
854.00 |
None |
Innovator Multiple Source Drug |
9636 |
None |
Raw materials, regulations |
None |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
Rx0000147 |
ASCEND Therapeutics US, LLC |
12/31/2019 |
17139040004 |
Binosto (alendronate sodium) Effervescent tablet for oral solution, 70mg, 4 tablets in 1 carton |
11/27/2019 |
98.40 |
300.00 |
08/11/2023 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
09/15/2019 |
Mission Pharmacal Company |
None |
1 |
None |
201.60 |
201.60 |
2012 |
140.00 |
None |
None |
Rx0000075 |
Assertio Therapeutics, Inc. |
03/31/2019 |
13913001201 |
Cambia (diclofenac potassium), 50MG, Oral, 1 Packet |
02/08/2019 |
6.81 |
75.62 |
06/16/2026 |
Single Source Drug |
1139039 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired in the past 5 years |
Rx0000075 |
Assertio Therapeutics, Inc. |
03/31/2019 |
13913000419 |
Gralise (gabapentin), 300MG, Oral Tablet, 90 Ct Bottle |
02/08/2019 |
75.62 |
839.42 |
02/26/2024 |
Single Source Drug |
1969210 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired in the past 5 years |
Rx0000075 |
Assertio Therapeutics, Inc. |
03/31/2019 |
13913000519 |
Gralise (gabapentin), 600MG, Oral Tablet, 90 Ct Bottle |
02/08/2019 |
75.62 |
839.42 |
02/26/2024 |
Single Source Drug |
15463198 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired in the past 5 years |
Rx0000075 |
Assertio Therapeutics, Inc. |
03/31/2019 |
13913000812 |
Zipsor (diclofenac potassium), 25MG, Oral Capsule, 100 Ct Bottle |
02/08/2019 |
128.73 |
1429.07 |
02/24/2029 |
Single Source Drug |
2365310 |
None |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired in the past 5 years |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469032014 |
CRESEMBA®186mg 14 Capsules |
01/08/2019 |
73.36 |
1295.91 |
10/31/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469052014 |
CRESEMBA®186mg 14 Capsules |
01/08/2019 |
73.36 |
1295.91 |
10/31/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469042099 |
CRESEMBA®372mg Vial |
01/08/2019 |
17.85 |
315.39 |
10/31/2020 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260171 |
Myrbetriq®25mg 100 Tablet |
01/08/2019 |
105.77 |
1280.98 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260130 |
Myrbetriq®25mg 30 Tablet |
01/08/2019 |
31.73 |
384.29 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260190 |
Myrbetriq®25mg 90 Tablet |
01/08/2019 |
95.19 |
1152.87 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260271 |
Myrbetriq®50mg 100 Tablet |
01/08/2019 |
105.77 |
1280.98 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260230 |
Myrbetriq®50mg 30 Tablet |
01/08/2019 |
31.73 |
384.29 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469260290 |
Myrbetriq®50mg 90 Tablet |
01/08/2019 |
95.19 |
1152.87 |
10/30/2028 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469060773 |
Prograf®0.5mg 100 Capsules |
01/08/2019 |
2.98 |
301.62 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469061711 |
Prograf®1mg 100 Capsules |
01/08/2019 |
5.97 |
603.24 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469061773 |
Prograf®1mg 100 Capsules |
01/08/2019 |
5.97 |
603.24 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469301601 |
Prograf®5mg 10 1ML Ampules |
01/08/2019 |
20.58 |
2079.09 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469065711 |
Prograf®5mg 100 Capsules |
01/08/2019 |
29.87 |
3016.22 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469065773 |
Prograf®5mg 100 Capsules |
01/08/2019 |
29.87 |
3016.22 |
None |
Innovator Multiple Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015152 |
VESIcare®10mg 100 Tablet |
01/08/2019 |
72.73 |
1285.03 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015101 |
VESIcare®10mg 30 Tablet |
01/08/2019 |
21.82 |
385.51 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015103 |
VESIcare®10mg 90 Tablet |
01/08/2019 |
65.46 |
1156.53 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015052 |
VESIcare®5mg 100 Tablet |
01/08/2019 |
72.73 |
1285.03 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015001 |
VESIcare®5mg 30 Tablet |
01/08/2019 |
21.82 |
385.51 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
51248015003 |
VESIcare®5mg 90 Tablet |
01/08/2019 |
65.46 |
1156.53 |
None |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000048 |
Astellas Pharma US, Inc. |
03/31/2019 |
00469012599 |
XTANDI®40mg 120 Capsules |
01/08/2019 |
643.41 |
11548.60 |
08/13/2027 |
Single Source Drug |
None |
1 |
None |
1 |
None |
1 |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
The information contained in this report is subject to the following limitations and assumptions. (1) Consistent with the relevant statutes and regulations, all information contained in this report is limited to that which Astellas believes is otherwise in the public domain or publicly available. (2) The patent expiration date contained in this report is limited to the patent information reported in the federal Food and Drug Administration’s Orange Book, as of April 22, 2019. As a result, the reported patent expiration date is limited to issued U.S. patents. Further, the reported patent expiration date does not reflect any pending patent applications, future filed patent applications, patent term extensions, data exclusivity (including orphan drug, pediatric, or other exclusivity), or patent-related litigation, each of which is speculative and which may extend or shorten the reported expiration date. (3) This product was not acquired, therefore columns 14-21 are intentionally left blank. |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310621030 |
Farxiga 10mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
1289346480 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
02/01/2014 |
Bristol-Myers Squibb |
2700000000 |
None |
AstraZeneca paid Bristol-Myers Squibb $2.7 billion of initial consideration. AstraZeneca has also agreed to pay up to $1.4 billion in regulatory, launch and sales payments, and various sales-related royalty payments up until 2025, $600 million of which relates to the approval of Farxiga in the US. In addition, AstraZeneca may make payments of up to $225 million when certain assets are subsequently transferred. |
289.20 |
None |
2014 |
289.20 |
None |
None |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310620530 |
Farxiga 5mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
599751771 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
02/01/2014 |
Bristol-Myers Squibb |
2700000000 |
None |
AstraZeneca paid Bristol-Myers Squibb $2.7 billion of initial consideration. AstraZeneca has also agreed to pay up to $1.4 billion in regulatory, launch and sales payments, and various sales-related royalty payments up until 2025, $600 million of which relates to the approval of Farxiga in the US. In addition, AstraZeneca may make payments of up to $225 million when certain assets are subsequently transferred. |
289.20 |
None |
2014 |
289.20 |
None |
None |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310628030 |
Xigduo XR 10-1000mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
129626100 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
AstraZeneca developed this NDC, it was not acquired within the last five years. |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310627030 |
Xigduo XR 10-500mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
13322599 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
AstraZeneca developed this NDC, it was not acquired within the last five years. |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310626060 |
Xigduo XR 5-1000mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
212483946 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
AstraZeneca developed this NDC, it was not acquired within the last five years. |
Rx0000015 |
AstraZeneca |
03/31/2019 |
00310625030 |
Xigduo XR 5-500mg |
01/01/2019 |
27.87 |
492.41 |
10/04/2025 |
Single Source Drug |
22269231 |
None |
AstraZeneca makes decisions on price revisions annually based on market conditions, a common practice across the industry. These decisions are designed to help us invest in bringing new medicines to market to address unmet patient needs and improve the lives of patients. When making pricing decisions AstraZeneca takes the following actions:
- We take into account not only the budget impact to payers but also consider patient out of pocket costs to ensure that our treatments reach the patients who need them.
- We seek feedback from payers and providers through meetings, advisory boards, and third party research.
- We price responsibly and in line with current treatment costs where treatment options exist.
- We consider factors such as Annual CPI-U rates and increases in manufacturing and transportation costs.
- We reinvest into R&D to identify future medicines to improve the lives of patients. |
None |
AstraZeneca is a science-led biopharmaceutical business, and our innovative medicines are used by millions of patients worldwide. Patients and science are at the heart of everything we do, and we put careful consideration into determining the value and ultimately the cost of our medicines. Many factors go into these decisions such as the benefits our medicines provide and their potential to reduce healthcare spending on other costlier medical procedures. Equally important, these decisions enable us to invest in discovering and developing future innovative medicines where new treatments are needed. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
AstraZeneca developed this NDC, it was not acquired within the last five years. |
Rx0000058 |
Avanir Pharmaceuiticals |
06/30/2019 |
64597030160 |
NUEDEXTA (Dextromethorphan hydrobromide 20 mg and quinidine sulfate 10 mg), Bottles of 60 capsules |
05/01/2019 |
76.00 |
1174.00 |
08/13/2026 |
Single Source Drug |
None |
1 |
None |
1 |
This WAC increase is not necessitated by a change or improvement in the prescription drug. |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
NOTE: columns 14-22 are intentionally blank since our product does not meet the requirements for completing these columns. |
Rx0000108 |
AvKare |
12/31/2019 |
50268068515 |
Prochlorperazine Maleate 10 MG Tablet 50 EA UD |
10/29/2019 |
30.22 |
73.93 |
None |
Non-innovator Multiple Source Drug |
1578 |
None |
Increase in Cost of Goods |
None |
There was no significant changes or improvements to this drug |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired |
Rx0000108 |
AvKare |
12/31/2019 |
50268068415 |
Prochlorperazine Maleate 5 MG Tablet 50 EA UD |
10/29/2019 |
25.90 |
67.14 |
None |
Non-innovator Multiple Source Drug |
1236 |
None |
Increase in Cost of Goods |
None |
There was no significant changes or improvements to this drug |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
None |
This drug was not acquired |