"70954-188-10" National Drug Code (NDC)

NDC Code	70954-188-10
Package Description	473 mL in 1 BOTTLE (70954-188-10)
Product NDC	70954-188
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20200713
Marketing Category Name	ANDA
Application Number	ANDA212252
Manufacturer	ANI 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]