# Ondansetron

NDC: 62135-878
Generic name: Ondansetron
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20061226

FDA application: ANDA077406

## Active ingredients

- ONDANSETRON: 16 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-878"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-878
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c74336c-11ec-420a-80e1-d8e4a8f1c46d