"63323-325-20" National Drug Code (NDC)

NDC Code	63323-325-20
Package Description	10 VIAL, SINGLE-DOSE in 1 TRAY (63323-325-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-325-09)
Product NDC	63323-325
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20001017
Marketing Category Name	ANDA
Application Number	ANDA074930
Manufacturer	Fresenius Kabi USA, LLC
Substance Name	ACYCLOVIR SODIUM
Strength	50
Strength Unit	mg/mL
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]