"68999-803-24" National Drug Code (NDC)

NDC Code	68999-803-24
Package Description	2 TRAY in 1 BOX (68999-803-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-803-05)
Product NDC	68999-803
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	Chartwell Governmental & Specialty RX, 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]