"70518-4100-1" National Drug Code (NDC)

NDC Code	70518-4100-1
Package Description	21 TABLET in 1 BOTTLE, PLASTIC (70518-4100-1)
Product NDC	70518-4100
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20240612
Marketing Category Name	ANDA
Application Number	ANDA209553
Manufacturer	REMEDYREPACK INC.
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Strength	1000
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]