Janssen |
50458002802 |
SPRAVATO Estekamine Nasal Spray 56mg (2X28mg) |
2019-03-08 |
590.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we are marketing in the US with print distribution and digital advertising in the mental health community, as well as promoting to appropriate healthcare professionals, systems of care and behavioral health clinics who treat individuals living with treatment resistant depression. The pricing plan has WAC set at $590 per package of 2 inhalers. The list price of SPRAVATO™ is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. SPRAVATO™ will also be discounted as required under the 340B program, the Federal Supply Schedule, and other government programs. Internationally, we are pursuing regulatory approvals for SPRAVATO for the treatment of treatment resistant depression. No approvals have been granted at this time. |
None |
None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed SPRAVATO is not available in the public domain, according to the National Institute of Mental Health, there are approximately 16.2 million patients with major depressive disorder (MDD) in the United States, and approximately 1/3 of MDD patients have treatment resistant depression (TRD). SPRAVATO will be clinically appropriate for a subset of patients with TRD. |
None |
Janssen |
50458002803 |
SPRAVATO Estekamine Nasal Spray 84mg (3X28mg) |
2019-03-08 |
885.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we are marketing in the US with print distribution and digital advertising in the mental health community, as well as promoting to appropriate healthcare professionals, systems of care and behavioral health clinics who treat individuals living with treatment resistant depression. The pricing plan has WAC set at $885 per package of 3 inhalers. The list price of SPRAVATO™ is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. SPRAVATO™ will also be discounted as required under the 340B program, the Federal Supply Schedule, and other government programs. Internationally, we are pursuing regulatory approvals for SPRAVATO for the treatment of treatment resistant depression. No approvals have been granted at this time. |
None |
None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed SPRAVATO is not available in the public domain, according to the National Institute of Mental Health, there are approximately 16.2 million patients with major depressive disorder (MDD) in the United States, and approximately 1/3 of MDD patients have treatment resistant depression (TRD). SPRAVATO will be clinically appropriate for a subset of patients with TRD. |
None |
Janssen |
59676003056 |
BALVERSA Erdafitinib 3mg 56 tablets |
2019-04-15 |
15120.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we plan to market in the US and promote to appropriate healthcare professionals who treat individuals living with metastatic urothelial cancer (mUC). The pricing plan has WAC set for 3mg 56 tablets at $15,120.00. The list price of BALVERSA is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. BALVERSA will also be discounted as required under the Federal Supply Schedule, and other government programs. There are no International approvals for BALVERSA. |
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None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed BALVERSA is not available in the public domain, BALVERSA is approved specifically for the treatment of patients with locally mUC harboring FGFR3 or FGFR2 genetic alterations. In the U.S., it is estimated that up to 3,000 people with urothelial carcinoma will test FGFR positive on an annual basis. Balversa was developed by Janssen. |
None |
Janssen |
59676003084 |
BALVERSA Erdafitinib 3mg 84 tablets |
2019-04-15 |
22680.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we plan to market in the US and promote to appropriate healthcare professionals who treat individuals living with metastatic urothelial cancer (mUC). The pricing plan has WAC set for 3mg 84 tablets at $22,680.00. The list price of BALVERSA is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. BALVERSA will also be discounted as required under the Federal Supply Schedule, and other government programs. There are no International approvals for BALVERSA. |
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None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed BALVERSA is not available in the public domain, BALVERSA is approved specifically for the treatment of patients with locally mUC harboring FGFR3 or FGFR2 genetic alterations. In the U.S., it is estimated that up to 3,000 people with urothelial carcinoma will test FGFR positive on an annual basis. Balversa was developed by Janssen. |
None |
Janssen |
59676004028 |
BALVERSA Erdafitinib 4mg 28 tablets |
2019-04-15 |
10080.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we plan to market in the US and promote to appropriate healthcare professionals who treat individuals living with metastatic urothelial cancer (mUC). The pricing plan has WAC set for 4mg 28 tablets at $10,080.00. The list price of BALVERSA is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. BALVERSA will also be discounted as required under the Federal Supply Schedule, and other government programs. There are no International approvals for BALVERSA. |
None |
None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed BALVERSA is not available in the public domain, BALVERSA is approved specifically for the treatment of patients with locally mUC harboring FGFR3 or FGFR2 genetic alterations. In the U.S., it is estimated that up to 3,000 people with urothelial carcinoma will test FGFR positive on an annual basis. Balversa was developed by Janssen. |
None |
Janssen |
59676004056 |
BALVERSA Erdafitinib 4mg 56 tablets |
2019-04-15 |
20160.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we plan to market in the US and promote to appropriate healthcare professionals who treat individuals living with metastatic urothelial cancer (mUC). The pricing plan has WAC set for 4mg 56 tablets at $20,160.00. The list price of BALVERSA is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. BALVERSA will also be discounted as required under the Federal Supply Schedule, and other government programs. There are no International approvals for BALVERSA. |
None |
None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed BALVERSA is not available in the public domain, BALVERSA is approved specifically for the treatment of patients with locally mUC harboring FGFR3 or FGFR2 genetic alterations. In the U.S., it is estimated that up to 3,000 people with urothelial carcinoma will test FGFR positive on an annual basis. Balversa was developed by Janssen. |
None |
Janssen |
59676005028 |
BALVERSA Erdafitinib 5mg 28 tablets |
2019-04-15 |
12600.0000 |
While specific marketing and pricing plans are not available in the public domain, generally we plan to market in the US and promote to appropriate healthcare professionals who treat individuals living with metastatic urothelial cancer (mUC). The pricing plan has WAC set for 5mg 28 tablets at $12,600.00. The list price of BALVERSA is not reflective of discounts and rebates which may be available through Medicaid, Medicare, and commercial insurance. BALVERSA will also be discounted as required under the Federal Supply Schedule, and other government programs. There are no International approvals for BALVERSA. |
None |
None |
1 |
1 |
None |
None |
None |
None |
While Janssen's estimated volume of patients who may be prescribed BALVERSA is not available in the public domain, BALVERSA is approved specifically for the treatment of patients with locally mUC harboring FGFR3 or FGFR2 genetic alterations. In the U.S., it is estimated that up to 3,000 people with urothelial carcinoma will test FGFR positive on an annual basis. Balversa was developed by Janssen. |
None |