FDA recall record

Lupin Pharmaceuticals Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 recall — FDA D-0090-2022

CGMP Deviations: impurity N-nitrosoirbesartan detected in API

Class IIclassification
D-0090-2022official record ID
Nov 10, 2021report date

Recall record at a glance

Official recordD-0090-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLupin Pharmaceuticals Inc.
Report dateNov 10, 2021
Recall initiation dateOct 12, 2021
Quantity98,052 bottles
LocationBaltimore, MD, United States

Official product description

Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only

Why the product was recalled

CGMP Deviations: impurity N-nitrosoirbesartan detected in API

Distribution information

Product was distributed to major distributors who may have further distributed the product nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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