"51660-905-03" National Drug Code (NDC)

NDC Code	51660-905-03
Package Description	10 TABLET in 1 BOTTLE (51660-905-03)
Product NDC	51660-905
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091125
Marketing Category Name	ANDA
Application Number	ANDA076588
Manufacturer	Ohm Laboratories 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]