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"58517-200-30" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (58517-200-30)
(New Horizon Rx Group, LLC)

NDC Code58517-200-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (58517-200-30)
Product NDC58517-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130813
Marketing Category NameANDA
Application NumberANDA090121
ManufacturerNew Horizon Rx Group, LLC
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/58517-200-30





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