"67296-1473-7" National Drug Code (NDC)

NDC Code	67296-1473-7
Package Description	21 TABLET, FILM COATED in 1 BOTTLE (67296-1473-7)
Product NDC	67296-1473
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir Hydrochloride
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20100524
Marketing Category Name	ANDA
Application Number	ANDA078518
Manufacturer	Redpharm Drug, Inc.
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 [EXT]