"50090-7270-0" National Drug Code (NDC)

NDC Code	50090-7270-0
Package Description	15 TABLET in 1 BOTTLE (50090-7270-0)
Product NDC	50090-7270
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	A-S Medication Solutions
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]