# Olanzapine

NDC: 72303-0843
Generic name: Olanzapine
Labeler / Manufacturer: HEC Pharm USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20260317

FDA application: ANDA208146

## Active ingredients

- OLANZAPINE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72303-0843"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72303-0843
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d1b83db-54db-d51f-e063-6394a90a4a69