RecallRadar

FDA Drug recall D-408-2014

Quinapril Tablets USP, 5 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 United States Man…

On 2014-01-22 the FDA classified a Class II recall of Quinapril Tablets USP, 5 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 United States Man… by Lupin Pharmaceuticals, citing failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-408-2014
ClassificationClass II
Statusterminated
Initiated2013-09-17
Published2014-01-22
Last updated2026-09-13 11:51 UTC
CompanyLupin Pharmaceuticals
DistributionUS

Product

Quinapril Tablets USP, 5 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 68180-556-09

Reason

Failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval

Identifiers

ndc68180-556-09
ndc68180-557-09
ndc68180-557-03
ndc68180-558-09
ndc68180-558-03
ndc68180-554-09
ndc68180-554-03
ndc68180-559-03
ndc68180-559-09
code_infoLots 3104879, 3104880, Exp. 10/13, 3110218, 3110219, 3110220 Exp. 12/13

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-408-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.