# Olanzapine

NDC: 70518-2337
Generic name: Olanzapine
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191002

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:"70518-2337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9eb6b0d1-b301-4847-88f5-f8613d550ecc