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"60687-103-25" National Drug Code (NDC)

Famciclovir 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-95)
(American Health Packaging)

NDC Code60687-103-25
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-95)
Product NDC60687-103
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamciclovir
Non-Proprietary NameFamciclovir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150331
End Marketing Date20200531
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 [EXT]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-103-25





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