"63629-1603-1" National Drug Code (NDC)

Propecia 30 TABLET, FILM COATED in 1 BOTTLE (63629-1603-1)
(Bryant Ranch Prepack)

NDC Code63629-1603-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (63629-1603-1)
Product NDC63629-1603
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePropecia
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19971219
Marketing Category NameNDA
Application NumberNDA020788
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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