Reported Apr 12, 2017 · Terminated
Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Lupin Pharmaceuticals Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Lupin Pharmaceuticals Inc. · 111 S Calvert St Fl 21ST · Baltimore, MD · 21202-6174
Is this the product you have?
- Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
- Lot codes and dates
Batch number G303703exp 3/2016
- Amount recalled
- 15,168 bottes
Where it was sold
- Nationwide
Why it was recalled
Failed Impurities/Degradation Specifications; Impurity A
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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