# Olanzapine

NDC: 31722-308
Generic name: Olanzapine
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20230322

FDA application: ANDA217466

## 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:"31722-308"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-308
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c1387008-6dc4-4f1e-ae29-fa7a0f0be684