"0173-0949-55" National Drug Code (NDC)

NDC Code	0173-0949-55
Package Description	100 TABLET in 1 BOTTLE (0173-0949-55)
Product NDC	0173-0949
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zovirax
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19930729
End Marketing Date	20150613
Marketing Category Name	NDA
Application Number	NDA020089
Manufacturer	GlaxoSmithKline LLC
Substance Name	ACYCLOVIR
Strength	400
Strength Unit	mg/1
Pharmacy Classes	DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]