NDC 50242-150 – Ocrevus

Ocrelizumab 300 mg/10mL · Injection · Intravenous

Human Prescription Drug

Product NDC50242-150

Product details

Brand name
Ocrevus
Generic name
Ocrelizumab
Labeler
Genentech, Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
BLA · BLA761053
Marketed since
March 28, 2017
Listing expires
December 31, 2027
Pharmacologic class
CD20-directed Cytolytic Antibody

Active ingredients

Uses, dosage, side effects and warnings for Ocrevus →

Package NDC codes (1)

Package NDCDescriptionSince
50242-150-011 VIAL, SINGLE-USE in 1 CARTON (50242-150-01) / 10 mL in 1 VIAL, SINGLE-USEMar 28, 2017