"17856-0090-1" National Drug Code (NDC)

Finasteride 1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)
(Atlantic Biologicals Corps)

NDC Code17856-0090-1
Package Description1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)
Product NDC17856-0090
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100528
Marketing Category NameANDA
Application NumberANDA090121
ManufacturerAtlantic Biologicals Corps
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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