"69367-262-09" National Drug Code (NDC)

NDC Code	69367-262-09
Package Description	90 TABLET in 1 BOTTLE (69367-262-09)
Product NDC	69367-262
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20230214
Marketing Category Name	ANDA
Application Number	ANDA209553
Manufacturer	Westminster Pharmaceuticals, LLC
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]