# Olanzapine

NDC: 70518-4729
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: 20260819

FDA application: ANDA202862

## Active ingredients

- OLANZAPINE: 2.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4729"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4729
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c47ee16f-5a86-49f2-8d85-5f49a6c8d91e