What FDA’s record states
| Field | What FDA’s record states | Source |
|---|---|---|
| Recipient | Apothecary Pharma, LLC | FDA letter ↗ |
| Location | Cary, NC | FDA letter ↗ |
| Letter date | Dec 1, 2025 | FDA letter ↗ |
| Posted by FDA | Mar 17, 2026 | FDA index ↗ |
| Issuing office | Center for Drug Evaluation and Research (CDER) | FDA letter ↗ |
| Subject | Compounding Pharmacy/Adulterated Drug Products | FDA letter ↗ |
| MARCS-CMS number | 717972 | FDA letter ↗ |
| GLP-1 drugs named | Semaglutide, Tirzepatide | FDA letter ↗ |
| Response letter | Not published by FDA | FDA letter ↗ |
| Closeout letter | Not published by FDA | FDA 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