"63187-920-21" National Drug Code (NDC)

Famciclovir 21 TABLET in 1 BOTTLE (63187-920-21)
(Proficient Rx LP)

NDC Code63187-920-21
Package Description21 TABLET in 1 BOTTLE (63187-920-21)
Product NDC63187-920
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20110321
Marketing Category NameANDA
Application NumberANDA078278
ManufacturerProficient Rx LP
Substance NameFAMCICLOVIR
Strength500
Strength Unitmg/1
Pharmacy ClassesDNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]

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