"61786-721-08" National Drug Code (NDC)

NDC Code	61786-721-08
Package Description	10 TABLET, FILM COATED in 1 BOTTLE (61786-721-08)
Product NDC	61786-721
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valtrex
Non-Proprietary Name	Valacyclovir Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20160526
Marketing Category Name	NDA
Application Number	NDA020487
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 [Chemical/Ingredient]