# OLANZAPINE

NDC: 13668-090
Generic name: OLANZAPINE
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20111025

FDA application: ANDA091415

## Active ingredients

- OLANZAPINE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13668-090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2cb1bebe-0ced-46d8-bf21-c28a9acc4a15