"67877-668-38" National Drug Code (NDC)

Febuxostat 10 BLISTER PACK in 1 CARTON (67877-668-38) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-668-38
Package Description10 BLISTER PACK in 1 CARTON (67877-668-38) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC67877-668
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFebuxostat
Non-Proprietary NameFebuxostat
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211208
Marketing Category NameANDA
Application NumberANDA212924
ManufacturerAscend Laboratories, LLC
Substance NameFEBUXOSTAT
Strength40
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

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