FDA Drug recall D-409-2014
Quinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 United States Ma…
- FDA Drug
- Class II
- terminated
- Published 2014-01-22
On 2014-01-22 the FDA classified a Class II recall of Quinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 United States Ma… by Lupin Pharmaceuticals, citing failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-409-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-17 |
| Published | 2014-01-22 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Lupin Pharmaceuticals |
| Distribution | US |
Product
Quinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 United States Manufactured by: Lupin Limited Goa 403 722 INDIA, NDC 68180-557-09
Reason
Failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval
Identifiers
| ndc | 68180-556-09 |
|---|---|
| ndc | 68180-557-09 |
| ndc | 68180-557-03 |
| ndc | 68180-558-09 |
| ndc | 68180-558-03 |
| ndc | 68180-554-09 |
| ndc | 68180-554-03 |
| ndc | 68180-559-03 |
| ndc | 68180-559-09 |
| code_info | Lot 3110358 Exp. 12/13 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-409-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.