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"70518-1704-0" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1704-0)
(REMEDYREPACK INC.)

NDC Code70518-1704-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1704-0)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1704-0





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