FDA warns Online Generic Medicine over unapproved injectable semaglutide

FDA warns Online Generic Medicine over unapproved injectable semaglutide

On 23 September 2026 the FDA’s Center for Drug Evaluation and Research issued a warning letter to the operator of www.onlinegenericmedicine.com, an internet pharmacy, after reviewing the site on 26 August and 2 September. The agency said the site offered U.S. consumers an injectable semaglutide product sold as “Semanat Injection (Semaglutide)”, which has no FDA … Read more

FDA warns Empower Pharmacy over compounded semaglutide and tirzepatide

FDA warns Empower Pharmacy over compounded semaglutide and tirzepatide

On September 18, 2026, the FDA issued a warning letter to Empower Clinic Services, LLC, doing business as Empower Pharmacy, of Houston, Texas, following an inspection of its facility in November 2025. The agency said the pharmacy compounded tirzepatide/niacinamide and semaglutide/cyanocobalamin products that appear to be essentially copies of FDA-approved drugs — the legal line … Read more

FDA warns five research-peptide sellers over GLP-1 products

FDA warns five research-peptide sellers over GLP-1 products

The FDA’s Center for Drug Evaluation and Research issued warning letters dated 24 August 2026 to five online peptide sellers — TXP Innovations LLC dba Tex Peptides, Royal Peptides LLC, NuScience Peptides LLC, Peptide Partners LLC and Peak Performance Peptides — posted 1 September 2026. Each followed a July 2026 review of the firm’s website … Read more

FDA warns BioDrive over its “GLP-1 biomimetic” peptide supplement

FDA warning letter to BioDrive over its Evolv GLP-1 Biomimetic peptide supplement

On 24 August 2026 the US Food and Drug Administration issued a warning letter to BioDrive, Inc. over Evolv GLP-1 Biomimetic, a dietary supplement whose labeling declares “Saccharomyces cerevisiae S288C EV-1 Peptide” as a dietary ingredient. FDA classed that ingredient as a new dietary ingredient and found the product adulterated under section 402(f)(1)(B) of the … Read more

FDA warning letter to Wholesale Peptide over Prostamax and gonadorelin

FDA warning letter to Wholesale Peptide over Prostamax and gonadorelin

On 17 June 2026 the FDA’s Center for Drug Evaluation and Research issued a warning letter to Wholesale Peptide of Brooksville, Florida, after reviewing the firm’s website in May 2026. The letter names two products, “Prostamax” and “Gonadorelin”, as unapproved new drugs under section 505(a) of the FD&C Act, quoting site copy stating that Prostamax … Read more

FDA warns five online peptide sellers over unapproved GLP-1 drugs

FDA warns five online peptide sellers over unapproved GLP-1 drugs

On 31 March 2026 the FDA’s Center for Drug Evaluation and Research issued warning letters to five websites selling injectable peptides to US buyers: Lovega LLC dba Pink Pony Peptides, Gram Peptides, Prime Sciences, Mile High Compounds and PekCura Labs. Each cites unapproved new drugs sold over the internet under sections 301(d) and 505(a) of … Read more

FDA warns 30 telehealth companies over compounded GLP-1 marketing

FDA warns 30 telehealth companies over compounded GLP-1 marketing

The FDA issued warning letters to 30 telehealth companies over false or misleading claims made about compounded GLP-1 products sold on their websites. It was the second wave of letters aimed at telehealth firms since the agency opened a broader campaign against misleading direct-to-consumer drug advertising in September 2025, and the largest single action against … Read more