"71335-0319-7" National Drug Code (NDC)

NDC Code	71335-0319-7
Package Description	40 TABLET in 1 BOTTLE (71335-0319-7)
Product NDC	71335-0319
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140910
Marketing Category Name	ANDA
Application Number	ANDA204314
Manufacturer	Bryant Ranch Prepack
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]