"55150-155-21" National Drug Code (NDC)

NDC Code	55150-155-21
Package Description	10 VIAL, SINGLE-DOSE in 1 CARTON (55150-155-21) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC	55150-155
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir Sodium
Non-Proprietary Name	Acyclovir Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20131011
Marketing Category Name	ANDA
Application Number	ANDA203701
Manufacturer	AuroMedics Pharma LLC
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 [EXT]