FDADecember 11, 2024drug

chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottle, RX only, Manufactured for: Glenmark Pharmaceuticals Inc., NJ; Product of India, NDC 68462-862-01

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

The hazard

CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.

What to do

FDA enforcement status: Ongoing

Brands named

glenmark pharmaceuticalsglenmark

Recall history

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

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