# Ondansetron

NDC: 51672-4091
Generic name: ondansetron hydrochloride
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20071130

FDA application: ANDA077009

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4091"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4091
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a95ca4f4-c4de-4822-9a08-209d10bf5136