Apotex Inc. recalls Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontari…
- Recall date
- April 7, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1081-2015
- FDA classification
- Class III
- Brand / firm
- Apotex Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Subpotent drug
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
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