"63739-495-40" National Drug Code (NDC)

Finasteride 100 TABLET, FILM COATED in 1 BOTTLE (63739-495-40)
(McKesson Packaging Services Business Unit of McKesson Corporation)

NDC Code63739-495-40
Package Description100 TABLET, FILM COATED in 1 BOTTLE (63739-495-40)
Product NDC63739-495
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101122
Marketing Category NameANDA
Application NumberANDA077914
ManufacturerMcKesson Packaging Services Business Unit of McKesson Corporation
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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