Class III · Lower riskRecall completed
Quinapril
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberBatch number G303703, exp 3/2016
Where it was soldNationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Failed Impurities/Degradation Specifications; Impurity A
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byLupin Pharmaceuticals, Inc.
| Brand name | QUINAPRIL |
| Generic name | QUINAPRIL |
| Active ingredient(s) | QUINAPRIL HYDROCHLORIDE |
| Distributed by / for | Lupin Pharmaceuticals Inc. |
| NDC | 68180-556-09 |
Show the full FDA record
| Full product label | Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09 |
| Recalling firm | Lupin Pharmaceuticals Inc. |
| Distribution | Nationwide |
| Quantity | 15,168 bottes |
| Recall initiated | 2015-12-07 |
| Report date | 2017-04-12 |
| Recall completed | 2017-04-10 |
| Recall number | D-0650-2017 |
| Classification | Class III |
| FDA status | Terminated |
| Origin on file | Baltimore MD United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.