"50436-0089-1" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (50436-0089-1)
(Unit Dose Services)

NDC Code50436-0089-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50436-0089-1)
Product NDC50436-0089
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131108
Marketing Category NameANDA
Application NumberANDA091643
ManufacturerUnit Dose Services
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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