"67877-288-33" National Drug Code (NDC)

Finasteride 1 BLISTER PACK in 1 CARTON (67877-288-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-288-33
Package Description1 BLISTER PACK in 1 CARTON (67877-288-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC67877-288
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170105
Marketing Category NameANDA
Application NumberANDA204304
ManufacturerAscend Laboratories, LLC
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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