"50242-127-01" National Drug Code (NDC)

NDC Code	50242-127-01
Package Description	1 VIAL, SINGLE-DOSE in 1 CARTON (50242-127-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC	50242-127
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Columvi
Non-Proprietary Name	Glofitamab
Dosage Form	CONCENTRATE
Usage	INTRAVENOUS
Start Marketing Date	20230615
Marketing Category Name	BLA
Application Number	BLA761309
Manufacturer	Genentech, Inc.
Substance Name	GLOFITAMAB
Strength	10
Strength Unit	mg/10mL
Pharmacy Classes	Bispecific CD20-directed CD3 T Cell Engager [EPC], CD20-directed Antibody Interactions [MoA], CD3 Receptor Agonists [MoA], CD3-directed Antibody Interactions [MoA], Cytochrome P450 Inhibitors [MoA], Increased Cytokine Activity [PE]