"68788-8705-3" National Drug Code (NDC)

NDC Code	68788-8705-3
Package Description	30 TABLET in 1 BOTTLE (68788-8705-3)
Product NDC	68788-8705
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20240701
Marketing Category Name	ANDA
Application Number	ANDA209553
Manufacturer	Preferred Pharmaceuticals Inc.
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Strength	1000
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]