"71335-0281-4" National Drug Code (NDC)

Finasteride 28 TABLET, FILM COATED in 1 BOTTLE (71335-0281-4)
(Bryant Ranch Prepack)

NDC Code71335-0281-4
Package Description28 TABLET, FILM COATED in 1 BOTTLE (71335-0281-4)
Product NDC71335-0281
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140920
Marketing Category NameANDA
Application NumberANDA203687
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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