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"71205-609-21" National Drug Code (NDC)

Famciclovir 21 TABLET, FILM COATED in 1 BOTTLE (71205-609-21)
(Proficient Rx LP)

NDC Code71205-609-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (71205-609-21)
Product NDC71205-609
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120113
Marketing Category NameANDA
Application NumberANDA201022
ManufacturerProficient Rx LP
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/71205-609-21





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