"70518-2117-1" National Drug Code (NDC)

NDC Code	70518-2117-1
Package Description	14 TABLET in 1 BLISTER PACK (70518-2117-1)
Product NDC	70518-2117
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190528
Marketing Category Name	ANDA
Application Number	ANDA203834
Manufacturer	REMEDYREPACK INC.
Substance Name	ACYCLOVIR
Strength	400
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]