RecallDepth
Class II Terminated

Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg, 100 tablet bottle, Rx only, Manufactured by for: Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by: Lupin Limited, Pithampur, INDIA NDC 68180-518-01

Company
Lupin Pharmaceuticals Inc.
Recall Initiated
July 17, 2019
Posted
August 21, 2019
Recall Number
D-1720-2019
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
39,216 bottles
Firm Location
Baltimore, MD, United States

Reason for Recall

Presence of Foreign Substance; Product complaints received related to brownish/blackish stains on the tablets and brownish/blackish powder observed inside the bottles.

Distribution

Product was distributed to wholesalers/distributors and supermarket and drug chains throughout the United States.

Lot / Code Info

Batch# H900575, exp. date 01/2022

More recalls by Lupin Pharmaceuticals Inc.

View all recalls by this company →

Other recent Class II Drug recalls