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"16714-522-05" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (16714-522-05)
(NorthStar Rx LLC)

NDC Code16714-522-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (16714-522-05)
Product NDC16714-522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110302
Marketing Category NameANDA
Application NumberANDA077914
ManufacturerNorthStar Rx 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/16714-522-05





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