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"0781-5620-31" National Drug Code (NDC)

Famciclovir 30 TABLET, FILM COATED in 1 BOTTLE (0781-5620-31)
(Sandoz Inc)

NDC Code0781-5620-31
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0781-5620-31)
Product NDC0781-5620
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110307
End Marketing Date20140831
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020363
ManufacturerSandoz Inc
Substance NameFAMCICLOVIR
Strength125
Strength Unitmg/1
Pharmacy ClassesDNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-5620-31





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