"72189-051-21" National Drug Code (NDC)

NDC Code	72189-051-21
Package Description	21 TABLET, FILM COATED in 1 BOTTLE (72189-051-21)
Product NDC	72189-051
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Valacyclovir
Non-Proprietary Name	Valacyclovir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200617
Marketing Category Name	ANDA
Application Number	ANDA203047
Manufacturer	DIRECT RX
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Strength	1
Strength Unit	g/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]