"70518-4417-0" National Drug Code (NDC)

NDC Code	70518-4417-0
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4417-0)
Product NDC	70518-4417
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20250731
Marketing Category Name	ANDA
Application Number	ANDA203047
Manufacturer	REMEDYREPACK 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]