"60687-103-21" National Drug Code (NDC)

Famciclovir 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-11)
(American Health Packaging)

NDC Code60687-103-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-11)
Product NDC60687-103
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150331
Marketing Category NameANDA
Application NumberANDA091480
ManufacturerAmerican Health Packaging
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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