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"17856-0708-1" National Drug Code (NDC)

Famciclovir 30 TABLET, FILM COATED in 1 BOTTLE (17856-0708-1)
(ATLANTIC BIOLOGICALS CORP.)

NDC Code17856-0708-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (17856-0708-1)
Product NDC17856-0708
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140910
Marketing Category NameANDA
Application NumberANDA202438
ManufacturerATLANTIC BIOLOGICALS CORP.
Substance NameFAMCICLOVIR
Strength500
Strength Unitmg/1
Pharmacy ClassesDNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/17856-0708-1





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