# Ondansetron

NDC: 68071-4115
Generic name: Ondansetron
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20070627

FDA application: ANDA078152

## Active ingredients

- ONDANSETRON: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5bacb621-1261-25d9-e053-2991aa0afa3b