# Ondansetron

NDC: 71205-713
Generic name: Ondansetron
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20100412

FDA application: ANDA090469

## Active ingredients

- ONDANSETRON: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-713"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-713
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47e26779-9465-410c-96b3-091119ae62f2