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"47335-721-13" National Drug Code (NDC)

Febuxostat 500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-721-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)
Product NDC47335-721
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFebuxostat
Non-Proprietary NameFebuxostat
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190705
Marketing Category NameANDA
Application NumberANDA205467
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFEBUXOSTAT
Strength40
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-721-13





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