"23155-485-51" National Drug Code (NDC)

NDC Code	23155-485-51
Package Description	473 mL in 1 BOTTLE (23155-485-51)
Product NDC	23155-485
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20200423
Marketing Category Name	ANDA
Application Number	ANDA212718
Manufacturer	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals 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]