Febuxostat 47335-0721-13

Package NDC

47335-0721-13

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	40 mg/1

Drug Class

Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]

Selected Package

47335-0721-13Selected

500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)

Other packages for this product(2)

47335-0721-81

90 TABLET, FILM COATED in 1 BOTTLE (47335-721-81)

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47335-0721-83

30 TABLET, FILM COATED in 1 BOTTLE (47335-721-83)

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