FDA recall D-1081-2015
Apotex Inc. · Class III · drug
Product
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
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2015-04-07
- Report date
- 2015-05-20
- Termination date
- 2017-04-07
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Toronto, N/A, Canada
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1081-2015