"51660-904-03" National Drug Code (NDC)

NDC Code	51660-904-03
Package Description	10 TABLET in 1 BOTTLE (51660-904-03)
Product NDC	51660-904
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	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]