FDAFDA · Food and drugs·Recall number D-1081-2015
Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
Published May 20, 2015 · Recall initiated: April 7, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent drug
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Apotex Inc.
- Distributor
- Nationwide
- Lot
- Lot # KL0664, Exp 04/15
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- Canada
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