Recalls / Active ingredient / Fenofibrate
Fenofibrate
3 FDA drug recalls involving the active ingredient “Fenofibrate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-03-13 | Class II | Fenofibrate Capsules 67 mg, USP, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, | Glenmark Pharmaceuticals Inc., USA |
| 2021-03-15 | Class II | FENOFIBRATE CAPSULES, UPS 67MG 100 CAPSULES NDC/UPC 27241-118-04; RX; CAPSULES | Cardinal Health Inc. |
| 2018-09-12 | Class III | Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Pis | Hetero Labs, Ltd. - Unit III |