"67296-1297-1" National Drug Code (NDC)

NDC Code	67296-1297-1
Package Description	21 TABLET, FILM COATED in 1 BOTTLE (67296-1297-1)
Product NDC	67296-1297
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20150525
Marketing Category Name	ANDA
Application Number	ANDA203047
Manufacturer	RedPharm Drug, 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]