# Ondansetron

NDC: 51407-004
Generic name: Ondansetron
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070625

FDA application: ANDA077851

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51407-004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b9ea1fc-59a4-8189-e063-6394a90a9ae6