# Ondansetron Hydrochloride

NDC: 85509-1057
Generic name: Ondansetron Hydrochloride
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070731

FDA application: ANDA078539

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-1057"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1057
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40106070-6a25-5b0e-e063-6394a90a4197