"72205-170-72" National Drug Code (NDC)

NDC Code	72205-170-72
Package Description	473 mL in 1 BOTTLE (72205-170-72)
Product NDC	72205-170
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir Suspension
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20230309
Marketing Category Name	ANDA
Application Number	ANDA217393
Manufacturer	Novadoz Pharmaceuticals LLC
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]