"68071-5122-5" National Drug Code (NDC)

NDC Code	68071-5122-5
Package Description	35 TABLET in 1 BOTTLE (68071-5122-5)
Product NDC	68071-5122
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130808
Marketing Category Name	ANDA
Application Number	ANDA074891
Manufacturer	NuCare Pharmaceuticals,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]