# OLANZAPINE

NDC: 72303-0840
Generic name: Olanzapine
Labeler / Manufacturer: HEC Pharm USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181130

FDA application: ANDA206238

## 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:"72303-0840"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72303-0840
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d34f8f3-edc8-0a68-e063-6394a90a9c1f