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"16714-522-10" National Drug Code (NDC)

Finasteride 1 BLISTER PACK in 1 DOSE PACK (16714-522-10) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(NorthStar Rx LLC)

NDC Code16714-522-10
Package Description1 BLISTER PACK in 1 DOSE PACK (16714-522-10) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC16714-522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110516
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/16714-522-10





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