"71205-767-90" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (71205-767-90)
(Proficient Rx LP)

NDC Code71205-767-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71205-767-90)
Product NDC71205-767
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170105
Marketing Category NameANDA
Application NumberANDA204304
ManufacturerProficient Rx LP
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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