# ONDANSETRON

NDC: 63187-236
Generic name: ONDANSETRON
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070625

FDA application: ANDA077851

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41c0dc3d-a616-425e-9073-625a0cb692c4