# ondansetron

NDC: 55154-7879
Generic name: ondansetron hydrochloride
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20061226

FDA application: ANDA076183

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-7879"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-7879
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb02f2d7-31a9-4f12-880e-7ce7d85440d4