Recalls / Active ingredient / Enalapril Maleate
Enalapril Maleate
6 FDA drug recalls involving the active ingredient “Enalapril Maleate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-03-16 | Class II | Enalapril Maleate Tablets, USP; 10 mg; 90 tablets, NDC 60429-185-90; manufactured by Taro Pharmaceutical Indus | Golden State Medical Supply Inc. |
| 2022-03-16 | Class II | Enalapril Maleate Tablets, USP; 5 mg; 90 tablets, NDC 60429-184-90; manufactured by Taro Pharmaceutical Indust | Golden State Medical Supply Inc. |
| 2022-03-16 | Class II | Enalapril Maleate Tablets, USP; 20 mg; 90 tablets, NDC 60429-186-90; manufactured by Taro Pharmaceutical Indus | Golden State Medical Supply Inc. |
| 2022-03-16 | Class II | Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharmaceutical Indu | Golden State Medical Supply Inc. |
| 2014-05-21 | Class III | Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets, NDC 0187-0146-01, 100 ct. bottles manufac | Valeant Pharmaceuticals North America LLC |
| 2014-05-21 | Class III | Vasotec (enalapril maleate) tablets, RX only, Manufactured by Valeant Pharmaceuticals International, Inc., Ste | Valeant Pharmaceuticals North America LLC |