# Olanzapine

NDC: 42658-152
Generic name: Olanzapine
Labeler / Manufacturer: Hisun Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250101

FDA application: ANDA206924

## Active ingredients

- OLANZAPINE: 7.5 mg/7.5mg

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42658-152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42658-152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0bbf07bd-400d-4f2a-e063-6294a90a1ed4