FDAMarch 22, 2017drug

Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (NDC 62756-556-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Ha...

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

The hazard

Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).

What to do

FDA enforcement status: Terminated

Brands named

sun pharmaceuticalsun

Recall history

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

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