"55390-613-20" National Drug Code (NDC)

NDC Code	55390-613-20
Package Description	10 VIAL in 1 BOX (55390-613-20) > 20 mL in 1 VIAL
Product NDC	55390-613
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir Sodium
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	19970423
End Marketing Date	20150130
Marketing Category Name	ANDA
Application Number	ANDA074596
Manufacturer	Bedford Laboratories
Substance Name	ACYCLOVIR SODIUM
Strength	1000
Strength Unit	mg/20mL
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 [Chemical/Ingredient]