# Ondansetron

NDC: 70518-4685
Generic name: Ondansetron
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20260629

FDA application: ANDA078152

## Active ingredients

- ONDANSETRON: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4685"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4685
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c3ad9c1-474e-4331-a017-09cec46702d8