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"63739-495-41" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (63739-495-41)
(McKesson Packaging Services Business Unit of McKesson Corporation)

NDC Code63739-495-41
Package Description30 TABLET, FILM COATED in 1 BOTTLE (63739-495-41)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-495-41





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