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"64980-351-03" National Drug Code (NDC)

Famciclovir 30 TABLET, FILM COATED in 1 BOTTLE (64980-351-03)
(Rising Pharma Holdings, Inc.)

NDC Code64980-351-03
Package Description30 TABLET, FILM COATED in 1 BOTTLE (64980-351-03)
Product NDC64980-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110321
Marketing Category NameANDA
Application NumberANDA091114
ManufacturerRising Pharma Holdings, Inc.
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/64980-351-03





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