# ONDANSETRON

NDC: 51662-1514
Generic name: ONDANSETRON
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20200331

FDA application: ANDA090469

## 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:"51662-1514"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1514
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a22a94bc-4fa7-8a4e-e053-2a95a90a6308