# Olanzapine

NDC: 0781-9105
Generic name: Olanzapine
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20111024

FDA application: ANDA201588

## Active ingredients

- OLANZAPINE: 10 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-9105"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-9105
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c44a96cc-817d-4eb5-a13a-00977f76e666