"70518-2032-0" National Drug Code (NDC)

NDC Code	70518-2032-0
Package Description	30 TABLET in 1 BLISTER PACK (70518-2032-0)
Product NDC	70518-2032
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190419
Marketing Category Name	ANDA
Application Number	ANDA210401
Manufacturer	REMEDYREPACK INC.
Substance Name	ACYCLOVIR
Strength	800
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]