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"51079-321-56" National Drug Code (NDC)

Finasteride 10 DOSE PACK in 1 CARTON (51079-321-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-321-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)
(Mylan Institutional Inc.)

NDC Code51079-321-56
Package Description10 DOSE PACK in 1 CARTON (51079-321-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-321-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)
Product NDC51079-321
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150713
End Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA077578
ManufacturerMylan Institutional Inc.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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