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
Reported: May 20, 2015 Initiated: April 7, 2015 #D-1079-2015
Product Description
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
Reason for Recall
Subpotent drug
Details
- Recalling Firm
- Apotex Inc.
- Units Affected
- 23,274 bottles/ blister cartons
- Distribution
- Nationwide
- Location
- Toronto, N/A
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Apotex Inc.. Units affected: 23,274 bottles/ blister cartons.
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-1079-2015.
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