Recalls / Active ingredient / Phentermine Hydrochloride
Phentermine Hydrochloride
5 FDA drug recalls involving the active ingredient “Phentermine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-05-09 | Class II | Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, | KVK Tech, Inc. |
| 2020-03-18 | Class II | Phentermine Hydrochloride Capsules, USP 15mg, 100-count bottles, Distributed by: Aurobindo Phama USA, Inc. Day | Aurobindo Pharma USA Inc. |
| 2017-08-11 | Class III | Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) | PD-Rx Pharmaceuticals, Inc. |
| 2017-08-03 | Class III | Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bo | KVK-Tech, Inc. |
| 2015-07-21 | Class III | Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 7-count (NDC 55289-791-07), b) 14-count (NDC 5 | PD-Rx Pharmaceuticals, Inc. |