"0093-7355-98" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7355-98
Package Description90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)
Product NDC0093-7355
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20061215
Marketing Category NameANDA
Application NumberANDA076511
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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