RECALL ALERT
Terminated
XLSX-B746A16B31
Lupin: Metformin Hydrochloride Extended-Release Tablets, 500mg and 1000mg
Recalled by Lupin Pharmaceuticals, Inc.
Classification
—
Reason for Recall
N-Nitrosodimethylamine (NDMA) Impurity
Product Details
Product Quantity
Not specified
Product Type
Food
Code Info
Not specified
Voluntary/Mandated
Not specified
Distribution & Geography
Distribution Pattern
Not specified
Company Location
Not specified
Timeline
Report Date
07/08/2020
Recall Initiated
07/08/2020
Classification Date
N/A
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: September 7, 2026
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