MedPath

ZINBRYTA

ZINBRYTA

Discontinued
DIN Number

02459639

Drug Class

Human

Market Date

N/A

Company
HC

Biogen Canada 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 Number02459639
AIG Number0158650001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription ,  Schedule D
A
ATC Code
L04AC01 DACLIZUMAB
Product Specifications
Dosage FormSolution
Route of AdministrationSubcutaneous
AHFS Classification92:20.00
Health Canada Classification

ACTIVE INGREDIENTS (1)

DACLIZUMAB BETAActive
Strength: 150 MG / ML
Monograph: DACLIZUMAB BETA

MedPath

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

© 2025 MedPath, Inc. All rights reserved.