"69117-0039-2" National Drug Code (NDC)

NDC Code	69117-0039-2
Package Description	500 CAPSULE in 1 BOTTLE (69117-0039-2)
Product NDC	69117-0039
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20210312
Marketing Category Name	ANDA
Application Number	ANDA212173
Manufacturer	YILING PHARMACEUTICAL, INC.
Substance Name	ACYCLOVIR
Strength	200
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]