Apotex Corp. recalls Olanzapine Orally Disintegrating Tablets 5 mg, 30-count Bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Ca
Recalled October 1, 2014 · FDA recall D-1609-2014 · Apotex
Hazard
Subpotent Drug: Out of specification (OOS) results at the 9 month temperature point. · FDA Class III
Units
5,397 bottles
Sold at
Nationwide.
Description
Subpotent Drug: Out of specification (OOS) results at the 9 month temperature point.
Product
Olanzapine Orally Disintegrating Tablets 5 mg, 30-count Bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada M9L1T9, Manufactured for Apotex Corp., Weston, Florida 33326, NDC # 60505-3275-03
Manufacturer(s)
Apotex Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →