"66689-342-16" National Drug Code (NDC)

NDC Code	66689-342-16
Package Description	1 BOTTLE in 1 CARTON (66689-342-16) > 473 mL in 1 BOTTLE
Product NDC	66689-342
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20210927
Marketing Category Name	ANDA
Application Number	ANDA213951
Manufacturer	VistaPharm, Inc.
Substance Name	ACYCLOVIR
Strength	200
Strength Unit	mg/5mL
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]