FDAFDA · Food and drugs·Recall number D-409-2014
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
Published January 22, 2014 · Recall initiated: September 17, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- QUINAPRIL
- Manufacturer
- Lupin Pharmaceuticals Inc.
- Distributor
- Nationwide and Puerto Rico
- UPC
- 0368180559092
- Lot
- Lot 3110358 Exp. 12/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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