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Updated:   2026-04-07

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Measure
Authors Gipson  
Subject Pharmacy Law: compounded medications: consumer protection.
Relating To relating to healing arts.
Title An act to add Article 10.5 (commencing with Section 4157) to Chapter 9 of Division 2 of the Business and Professions Code, relating to healing arts.
Last Action Dt 2026-03-09
State Amended Assembly
Status In Committee Process
Flags
Vote Req Approp Fiscal Cmte Local Prog Subs Chgs Urgency Tax Levy Active?
Majority No Yes Yes None No No Y
i
Leginfo Link  
Bill Actions
2026-03-24     In committee: Hearing postponed by committee.
2026-03-10     Re-referred to Com. on B. & P.
2026-03-09     Referred to Coms. on B. & P. and P. & C.P.
2026-03-09     From committee chair, with author's amendments: Amend, and re-refer to Com. on B. & P. Read second time and amended.
2026-02-18     From printer. May be heard in committee March 20.
2026-02-17     Read first time. To print.
Versions
Amended Assembly     2026-03-09
Introduced     2026-02-17
Analyses TBD
Latest Text Bill Full Text
Latest Text Digest

Existing law, the Pharmacy Law, requires the California State Board of Pharmacy within the Department of Consumer Affairs to license and regulate the practice of pharmacy, including pharmacists, pharmacy technicians, and pharmacies. Under existing law, it is unlawful for any person to manufacture, compound, furnish, sell, or dispense a dangerous drug or dangerous device, or to dispense or compound a prescription unless they are licensed, as specified. A violation of that law is a crime.

Existing law also requires the compounding of drug preparations by a pharmacy for furnishing, distribution, or use to be consistent with standards established in the pharmacy compounding chapters of the current version of the United States Pharmacopeia-National Formulary, including relevant testing and quality assurance. Existing law authorizes advertisements for prescription drugs, if the advertisement conforms with certain requirements, including not containing a false, fraudulent, misleading, or deceptive statement.

This bill would make it unlawful for a person or entity to engage in the sale, transfer, or distribution of a compounded drug using a drug substance that is a glucose-dependent insulinotropic polypeptide receptor or glucagon-like-peptide-1 receptor agonist used for obesity or weight management or a drug substance that is a component of a similar drug approved by the federal Food and Drug Administration for obesity or weight management unless the compounder of the drug takes specified actions. These acts would include ensuring that the bulk drug substance, as defined, is a pharmaceutical grade product and is accompanied by a valid certificate of analysis. The bill would also make it unlawful for a manufacturer or wholesaler to sell, transfer, or distribute a bulk drug substance for use in compounding without providing to the purchaser written verification that the bulk drug substance meets specified conditions, including being pharmaceutical grade. The bill would make a violation of these provisions punishable by a fine of $1,000 per dose of the illegally compounded drug sold, transferred, or distributed and license revocation.

The bill would require any person or entity engaging in the sale, transfer, or distribution of compounded drugs to maintain all records related to the acquisition, examination, and testing of the bulk drug substance for not less than 2 years after the expiration date of the last lot of drug containing the bulk drug substance and, upon request, to furnish that information to the board. The bill would authorize the board or its duly authorized agent to inspect any person or entity that engages in compounding drugs, as prescribed.