Class II
Terminated
Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-558-09
- Company
- Lupin Pharmaceuticals Inc.
- Recall Initiated
- December 7, 2022
- Posted
- December 28, 2022
- Recall Number
- D-0089-2023
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 23,736
- Firm Location
- Baltimore, MD, United States
Reason for Recall
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Distribution
Product was distributed by major distribution chains nationwide.
Lot / Code Info
Lot #: G102929, Exp 04/2023
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