Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC ...
FDA Recall #D-0650-2017 — Class III — December 7, 2015
Product Description
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
Recalling Firm
Lupin Pharmaceuticals Inc. — Baltimore, MD
Classification
Class III — Not likely to cause adverse health consequences.
Product Type
Drugs
Product Quantity
15,168 bottes
Distribution
Nationwide
Code Information
Batch number G303703, exp 3/2016
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated