# ONDANSETRON

NDC: 62135-350
Generic name: ONDANSETRON
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070625

FDA application: ANDA077303

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-350"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-350
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=88b7432b-f5a7-40f3-9b0c-e7b125f5103c