"71335-1898-3" National Drug Code (NDC)

Finasteride 60 TABLET, FILM COATED in 1 BOTTLE (71335-1898-3)
(Bryant Ranch Prepack)

NDC Code71335-1898-3
Package Description60 TABLET, FILM COATED in 1 BOTTLE (71335-1898-3)
Product NDC71335-1898
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170105
Marketing Category NameANDA
Application NumberANDA204304
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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