# Olanzapine

NDC: 60505-3112
Generic name: Olanzapine
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120423

FDA application: ANDA090798

## Active ingredients

- OLANZAPINE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-3112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-3112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3347d1c8-04c9-5ce1-8cda-b38e0412b709