# Ondansetron

NDC: 69339-172
Generic name: Ondansetron
Labeler / Manufacturer: Natco Pharma USA LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221024

FDA application: ANDA077851

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69339-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69339-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=64527de5-0b92-4340-9243-7a37e8ff96d9