fda warning letters compounded semaglutide tirzepatide september 2025 Issues to 30 Telehealth Companies Over Misleading GLP-1 RA Marketing FDA issued 25 warning letters

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FDA issued 25 warning letters to telehealth companies for false and misleading claims about compounded GLP 1 products. Unlike FDA approved drugs, these products have not been proven to be safe, effective, or of The FDA sent a warning letter to the maker of Ozempic and Wegovy over unreported potential GLP 1 side effects. Click the link in bio to learn what you need to know. FDA telehealth crackdown highlights role of national doctor networks Article: Brazilian Clinics and the False Equivalence of Compounded GLP 1 Drugs: ANVISA should follow FDA The FDA has strictly clarified that with the national supply of GLP 1 medications stabilizing, compounders can no longer produce "essentially copies" of FDA approved drugs. Enforcement discretion periods for drugs like semaglutide and September 2, 2025: U.S. compounding restrictions have stemmed a flood of compounded semaglutide and tirzepatide Partnership for Safe Medicines

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