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"70518-3616-5" National Drug Code (NDC)

Finasteride 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)
(REMEDYREPACK INC.)

NDC Code70518-3616-5
Package Description100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)
Product NDC70518-3616
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230118
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/70518-3616-5





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