# Ondansetron

NDC: 83008-026
Generic name: Ondansetron
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20230512
Marketing ended: 20260630
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:"83008-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83008-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=318c2f90-d4ad-49e7-b885-cfb132b4cd17