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"61919-733-90" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (61919-733-90)
(Direct_Rx)

NDC Code61919-733-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-733-90)
Product NDC61919-733
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190118
Marketing Category NameANDA
Application NumberANDA090121
ManufacturerDirect_Rx
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/61919-733-90





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