"16714-305-01" National Drug Code (NDC)

Famciclovir 30 TABLET, FILM COATED in 1 BOTTLE (16714-305-01)
(NorthStar Rx LLC)

NDC Code16714-305-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE (16714-305-01)
Product NDC16714-305
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110321
Marketing Category NameANDA
Application NumberANDA091114
ManufacturerNorthStar Rx LLC
Substance NameFAMCICLOVIR
Strength500
Strength Unitmg/1
Pharmacy ClassesDNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

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