"0054-0114-13" National Drug Code (NDC)

NDC Code	0054-0114-13
Package Description	30 TABLET in 1 BOTTLE (0054-0114-13)
Product NDC	0054-0114
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20100524
End Marketing Date	20190130
Marketing Category Name	ANDA
Application Number	ANDA078656
Manufacturer	West-Ward Pharmaceuticals Corp.
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Strength	500
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]