WhichRecall
Class IIReported 2025-07-23

Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, Manufactured by: Lupin Limited Nagpur-441 108, INDIA, NDC 68180-519-01

Recalled by Lupin Pharmaceuticals Inc.

Reason for Recall

Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.

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Recall Number
D-0532-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-06-20
Reported
2025-07-23
Distribution
Product was distributed nationwide within the United States.
Code Info
Lot #: QA01081, Exp. Date April 2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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