"68071-4345-5" National Drug Code (NDC)

NDC Code	68071-4345-5
Package Description	35 TABLET in 1 BOTTLE (68071-4345-5)
Product NDC	68071-4345
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20161015
Marketing Category Name	ANDA
Application Number	ANDA202168
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]