# Olanzapine

NDC: 72241-052
Generic name: Olanzapine
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230227

FDA application: ANDA210022

## Active ingredients

- OLANZAPINE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0943b4e-6bdc-48c1-8ecd-39cf732e16f5