ocrelizumab

FDA Drug Profile — OCREVUS

ocrelizumab is listed in the FDA National Drug Code directory with 4 NDC codes, marketed under brand name including OCREVUS. Available dosage forms: liquid, injection.

Drug Details

Generic Name
ocrelizumab
Brand Names
OCREVUS
Application Number
BLA761053
Sponsor
Lonza Biologics, Inc.
NDC Codes
4
Dosage Forms
LIQUID, INJECTION
Routes
INTRAVENOUS
Active Ingredients
OCRELIZUMAB

Indications and Usage

1 INDICATIONS AND USAGE OCREVUS is indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults Primary progressive MS, in adults Relapsing-remitting MS, in pediatric patients 10 years of age and older who weigh 25 kg or more. OCREVUS is a CD20-directed cytolytic antibody indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults ( 1 ) Primary progressive MS, in adults ( 1 ) Relapsing-remitting MS, in pediatric patients 10 years of age and older who weigh 25 kg or more ( 1 )