"70518-0323-0" National Drug Code (NDC)

NDC Code	70518-0323-0
Package Description	4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0323-0)
Product NDC	70518-0323
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20170316
Marketing Category Name	ANDA
Application Number	ANDA076588
Manufacturer	REMEDYREPACK INC.
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Strength	1
Strength Unit	g/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]