"68084-399-01" National Drug Code (NDC)

Finasteride 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-399-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-399-11)
(American Health Packaging)

NDC Code68084-399-01
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-399-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-399-11)
Product NDC68084-399
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120124
End Marketing Date20190731
Marketing Category NameANDA
Application NumberANDA077914
ManufacturerAmerican Health Packaging
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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