"61919-515-20" National Drug Code (NDC)

NDC Code	61919-515-20
Package Description	20 TABLET in 1 BOTTLE (61919-515-20)
Product NDC	61919-515
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190424
Marketing Category Name	ANDA
Application Number	ANDA077135
Manufacturer	DirectRX
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]