"50242-150-01" National Drug Code (NDC)

NDC Code	50242-150-01
Package Description	1 VIAL, SINGLE-USE in 1 CARTON (50242-150-01) / 10 mL in 1 VIAL, SINGLE-USE
Product NDC	50242-150
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ocrevus
Non-Proprietary Name	Ocrelizumab
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20170328
Marketing Category Name	BLA
Application Number	BLA761053
Manufacturer	Genentech, Inc.
Substance Name	OCRELIZUMAB
Strength	300
Strength Unit	mg/10mL
Pharmacy Classes	Antibodies, Monoclonal [CS], Antibodies, Monoclonal, Humanized [CS], CD20-directed Antibody Interactions [MoA], CD20-directed Cytolytic Antibody [EPC]