# Ondansetron

NDC: 0143-9891
Generic name: Ondansetron
Labeler / Manufacturer: West-Ward Pharmaceuticals Corp
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20061226

FDA application: ANDA076780

## 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:"0143-9891"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9891
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb4bc810-db26-471b-9ce7-6e2fb3018af0