# Olanzapine

NDC: 0527-3162
Generic name: Olanzapine
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20230530

FDA application: ANDA208146

## Active ingredients

- OLANZAPINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-3162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-3162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=002dd00f-7946-ea4f-e063-6294a90a5916