"70518-1704-1" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1704-1)
(REMEDYREPACK INC.)

NDC Code70518-1704-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1704-1)
Product NDC70518-1704
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181130
Marketing Category NameANDA
Application NumberANDA078341
ManufacturerREMEDYREPACK INC.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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