Febuxostat 47335-0722
Product NDC
47335-0722- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 5, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA205467
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Febuxostat | 80 mg/1 |
Drug Class
Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]
Packaging Options(3)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-722-18)
30 TABLET, FILM COATED in 1 BOTTLE (47335-722-83)
100 TABLET, FILM COATED in 1 BOTTLE (47335-722-88)