"72189-594-16" National Drug Code (NDC)

NDC Code	72189-594-16
Package Description	16 TABLET in 1 BOTTLE (72189-594-16)
Product NDC	72189-594
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20241111
Marketing Category Name	ANDA
Application Number	ANDA209553
Manufacturer	Direct _Rx
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]