FDAApril 7, 2015drug

Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 60505-3275-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9

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

The hazard

Subpotent drug

What to do

FDA enforcement status: Terminated

Brands named

apotex

UPCs

6050532750360505327500

Recall history

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

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