"23155-229-01" National Drug Code (NDC)

NDC Code	23155-229-01
Package Description	100 CAPSULE in 1 BOTTLE (23155-229-01)
Product NDC	23155-229
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20140602
Marketing Category Name	ANDA
Application Number	ANDA074889
Manufacturer	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance Name	ACYCLOVIR
Strength	200
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]