"70771-1152-4" National Drug Code (NDC)

Finasteride 10 BLISTER PACK in 1 CARTON (70771-1152-4) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Zydus Lifesciences Limited)

NDC Code70771-1152-4
Package Description10 BLISTER PACK in 1 CARTON (70771-1152-4) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC70771-1152
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA078900
ManufacturerZydus Lifesciences Limited
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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