"58118-7355-8" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-7355-8)
(Clinical Solutions Wholesale)

NDC Code58118-7355-8
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (58118-7355-8)
Product NDC58118-7355
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20061215
Marketing Category NameANDA
Application NumberANDA076511
ManufacturerClinical Solutions Wholesale
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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