# Ondansetron Hydrochloride

NDC: 85509-1076
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: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-1076"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1076
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a76bae2-04c2-ee2d-e063-6394a90ad4c8