# Febuxostat

NDC: 47335-722
Generic name: Febuxostat
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190705

FDA application: ANDA205467

## Active ingredients

- FEBUXOSTAT: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-722"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-722
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f7541bd-bf32-422b-b99a-89193cf193ca