"71335-1304-1" National Drug Code (NDC)

Finasteride 30 TABLET, COATED in 1 BOTTLE (71335-1304-1)
(Bryant Ranch Prepack)

NDC Code71335-1304-1
Package Description30 TABLET, COATED in 1 BOTTLE (71335-1304-1)
Product NDC71335-1304
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20170106
Marketing Category NameANDA
Application NumberANDA207750
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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