"67046-1347-3" National Drug Code (NDC)

NDC Code	67046-1347-3
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1347-3)
Product NDC	67046-1347
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20260504
Marketing Category Name	ANDA
Application Number	ANDA203047
Manufacturer	Coupler LLC
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]