"61919-919-71" National Drug Code (NDC)

NDC Code	61919-919-71
Package Description	100 CAPSULE in 1 BOTTLE (61919-919-71)
Product NDC	61919-919
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20150101
Marketing Category Name	ANDA
Application Number	ANDA077478
Manufacturer	Direct Rx
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]