Recalls / Active ingredient / Telmisartan
Telmisartan
6 FDA drug recalls involving the active ingredient “Telmisartan” — 1 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2024-02-09 | Class II | Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722 | Micro Labs Limited |
| 2022-06-29 | Class II | Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark | Glenmark Pharmaceuticals Inc., USA |
| 2022-06-29 | Class II | Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark P | Glenmark Pharmaceuticals Inc., USA |
| 2021-05-04 | Class II | Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distrib | Boehringer Ingelheim Pharmaceuticals, Inc. |
| 2021-03-17 | Class I | Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (F | Alembic Pharmaceuticals Limited |
| 2019-04-01 | Class III | Telmisartan and Amlodipine Tablets 80 mg/5 mg, 30 tablet bottle, Rx only, Manufactured for: Lupin Pharmaceutic | Lupin Pharmaceuticals Inc. |