PlainRecalls
FDA Drug Low Class III Terminated

Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9

Reported: May 20, 2015 Initiated: April 7, 2015 #D-1081-2015

Product Description

Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9

Reason for Recall

Subpotent drug

Details

Recalling Firm
Apotex Inc.
Units Affected
5,352 bottles
Distribution
Nationwide
Location
Toronto, N/A

Frequently Asked Questions

What product was recalled?
Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9. Recalled by Apotex Inc.. Units affected: 5,352 bottles.
Why was this product recalled?
Subpotent drug
Which agency issued this recall?
This recall was issued by the FDA Drug on May 20, 2015. Severity: Low. Recall number: D-1081-2015.