"58118-0791-8" National Drug Code (NDC)

NDC Code	58118-0791-8
Package Description	30 TABLET in 1 BLISTER PACK (58118-0791-8)
Product NDC	58118-0791
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190617
Marketing Category Name	ANDA
Application Number	ANDA204314
Manufacturer	Clinical Solutions Wholesale, LLC
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]