RecallDepth
Class III Terminated

Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09

This recall has been terminated (originally issued April 12, 2017).

Company
Lupin Pharmaceuticals Inc.
Recall Initiated
December 7, 2015
Posted
April 12, 2017
Recall Number
D-0650-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
15,168 bottes
Firm Location
Baltimore, MD, United States
Official Source
View on FDA website ↗

Reason for Recall

Failed Impurities/Degradation Specifications; Impurity A

Distribution

Nationwide

Lot / Code Info

Batch number G303703, exp 3/2016

More recalls by Lupin Pharmaceuticals Inc.

View all recalls by this company →

Other recent Class III Drug recalls