"72162-1724-4" National Drug Code (NDC)

NDC Code	72162-1724-4
Package Description	35 TABLET in 1 BOTTLE (72162-1724-4)
Product NDC	72162-1724
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20060313
End Marketing Date	20261231
Marketing Category Name	ANDA
Application Number	ANDA077309
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]