"68071-3155-7" National Drug Code (NDC)

NDC Code	68071-3155-7
Package Description	35 TABLET in 1 BOTTLE (68071-3155-7)
Product NDC	68071-3155
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	NuCarePharmaceuticals, Inc.
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]