Drug recall D-0650-2017
Product
Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Reason for recall
Failed Impurities/Degradation Specifications; Impurity A
Lots and codes
Batch number G303703, exp 3/2016
Recall details
- Recalling firm
- Lupin Pharmaceuticals Inc., Baltimore, MD
- Quantity
- 15,168 bottes
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 7, 2015
- Terminated
- April 10, 2017
Related products
- Quinapril – drug information
- NDC 68180-554 Quinapril · Quinapril Hydrochloride 40 mg/1 · Lupin Pharmaceuticals, Inc.
- NDC 68180-558 Quinapril · Quinapril Hydrochloride 20 mg/1 · Lupin Pharmaceuticals, Inc.
- NDC 68180-559 Quinapril · Quinapril Hydrochloride 40 mg/1 · Lupin Pharmaceuticals, Inc.
- NDC 68180-557 Quinapril · Quinapril Hydrochloride 10 mg/1 · Lupin Pharmaceuticals, Inc.