"68071-3222-4" National Drug Code (NDC)

NDC Code	68071-3222-4
Package Description	14 TABLET in 1 BOTTLE (68071-3222-4)
Product NDC	68071-3222
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20131129
Marketing Category Name	ANDA
Application Number	ANDA203834
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]