MedPath

BENLYSTA

BENLYSTA

Approved
DIN Number

02370050

Drug Class

Human

Market Date

Aug 24, 2011

Company
HC

GlaxoSmithKline Inc

Product Information

Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.

Product Details

Health Canada regulatory and product classification information

Regulatory Identifiers
DIN Number02370050
AIG Number0152941002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription ,  Schedule D
A
ATC Code
L04AG04 BELIMUMAB
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification90:24.28
Health Canada Classification

ACTIVE INGREDIENTS (1)

BELIMUMABActive
Strength: 120 MG / VIAL
Monograph: BELIMUMAB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.