"40085-842-96" National Drug Code (NDC)

NDC Code	40085-842-96
Package Description	473 mL in 1 BOTTLE (40085-842-96)
Product NDC	40085-842
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20140903
End Marketing Date	20200131
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA019909
Manufacturer	Renaissance Pharma, Inc.
Substance Name	ACYCLOVIR
Strength	200
Strength Unit	mg/5mL
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]