fda warning letters compounded semaglutide 2025 Letter Breakdown: Sterility Failures, Subpotent GLP-1 Drugs, and a Compounding Pharmacy Operating Without Control Semaglutide Patient Safety Updates |

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Semaglutide Patient Safety Updates semaglutide.com Last month, the FDA issued 25 warning letters to telehealth companies over what it called false or misleading claims about compounded GLP 1 medications. 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 Fifth Circuit probes FDA ban on compounded GLP 1s Courthouse News Service

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