PriceTracker GLP-1

What FDA’s record states

FDA record for the warning letter to Apothecary Pharma, LLC
FieldWhat FDA’s record statesSource
RecipientApothecary Pharma, LLCFDA letter
LocationCary, NCFDA letter
Letter dateDec 1, 2025FDA letter
Posted by FDAMar 17, 2026FDA index
Issuing officeCenter for Drug Evaluation and Research (CDER)FDA letter
SubjectCompounding Pharmacy/Adulterated Drug ProductsFDA letter
MARCS-CMS number717972FDA letter
GLP-1 drugs namedSemaglutide, TirzepatideFDA letter
Response letterNot published by FDAFDA letter
Closeout letterNot published by FDAFDA letter
“Some of your facility’s drug products, such as Tirzepatide Injection 10 mg/mL and Semaglutide Injection 2.5 mg/mL, did not include the following information on the label: a list of active and inactive ingredients, identified by established name and the quantity or proportion of each ingredient.”FDA warning letter to Apothecary Pharma, LLC, Dec 1, 2025 · read the full letter on fda.gov ↗

What this is and is not.A warning letter is FDA’s statement of what it considers significant violations. It is an allegation, not a court finding, and the firm can respond. A closeout letter is posted when FDA confirms the violations were corrected.

Source

Every field above is copied from FDA’s page for this letter, read Oct 3, 2026. The letter on fda.gov ↗ · All 161 GLP-1 warning letters