FDAOctober 20, 2017drug

diphenoxylate hydrochloride and atropine sulfate tablets, USP, 2.5 mg/0.025 mg, a) 100-count bottle (NDC 59762-1061-1), b) 1000-count bottle (NDC 59762-1061-2), Rx Only, Distributed by: Greenstone LLC. Peapack, NJ 07977

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

The hazard

SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent

What to do

FDA enforcement status: Terminated

Brands named

pfizer

Recall history

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

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