# Ondansetron

NDC: 85766-199
Generic name: ONDANSETRON
Labeler / Manufacturer: Sportpharm LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20061107

FDA application: ANDA077473

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85766-199"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85766-199
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98c1413c-ff7f-4554-9e9f-289038b39ca6