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The FDA is proposing the removal of three GLP-1 drugs from the 503B bulks list of active ingredients that outsourcing facilities can use to make compounded medicines, the agency announced on Thursday
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Pharmacovigilance Assessment of Compounded GLP-1 Receptor Agonists: Insights From the FDA Adverse Event Reporting System
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Novo asks FDA to prevent compounders from making GLP-1 knockoffs
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FDA Intensifies Crackdown on GLP-1 Compounding
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Compounded" GLP-1 drugs | Health Communication Research Laboratory
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Hims & Hers stock falls 25% as FDA curtails compounded GLP-1s
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FDA is moving to restrict mass-marketed compounded GLP-1 products that aren't FDA-approved, warning companies they can't market them as equivalent to approved drugs and signaling stronger enforcement to protect patients from unverified
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