# Ondansetron

NDC: 55154-6976
Generic name: ONDANSETRON
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20081016

FDA application: ANDA077548

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-6976"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-6976
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1b9c2d9f-62a8-4d26-a041-a598bc59e300