"70518-2496-0" National Drug Code (NDC)

NDC Code	70518-2496-0
Package Description	30 CAPSULE in 1 BLISTER PACK (70518-2496-0)
Product NDC	70518-2496
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20191218
Marketing Category Name	ANDA
Application Number	ANDA074889
Manufacturer	REMEDYREPACK 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]