FDADecember 27, 2021drug

Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviations- Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.

What to do

FDA enforcement status: Terminated

Brands named

viona pharmaceuticalsviona

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01 — Recall Details · AllClear