Recalls / Active ingredient / Quinapril Hydrochloride
Quinapril Hydrochloride
6 FDA drug recalls involving the active ingredient “Quinapril Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-12-07 | Class II | Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Mary | Lupin Pharmaceuticals Inc. |
| 2022-12-07 | Class II | Quinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Mary | Lupin Pharmaceuticals Inc. |
| 2022-10-05 | Class II | Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharm | Aurobindo Pharma USA Inc. |
| 2015-12-07 | Class III | Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09 | Lupin Pharmaceuticals Inc. |
| 2013-09-17 | Class II | Quinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltim | Lupin Pharmaceuticals Inc. |
| 2013-09-17 | Class II | Quinapril Tablets USP, 5 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimo | Lupin Pharmaceuticals Inc. |