# Olanzapine

NDC: 67046-0072
Generic name: Olanzapine
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260619

FDA application: ANDA202862

## 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:"67046-0072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-0072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=549dc142-adcd-99ed-e063-6294a90a37fa