# Ondansetron

NDC: 17856-0672
Generic name: Ondansetron Hydrochloride
Labeler / Manufacturer: Atlantic Biologics Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20071128

FDA application: ANDA078776

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0672"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0672
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41d71d26-0d42-b368-e063-6394a90add43