# ONDANSETRON

NDC: 61919-986
Generic name: ONDANSETRON
Labeler / Manufacturer: Direct Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20140101

FDA application: ANDA090469

## 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:"61919-986"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-986
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b38feff2-900a-4e0c-8260-8f090edbc0bc