"68382-225-30" National Drug Code (NDC)

NDC Code	68382-225-30
Package Description	10 BLISTER PACK in 1 CARTON (68382-225-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	68382-225
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180405
Marketing Category Name	ANDA
Application Number	ANDA079137
Manufacturer	Zydus Pharmaceuticals (USA) 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]