MedPath

BIMZELX

BIMZELX

Approved
DIN Number

02553619

Drug Class

Human

Market Date

Apr 7, 2025

Company
HC

UCB 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 Number02553619
AIG Number0163399001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D ,  Prescription
A
ATC Code
L04AC21 BIMEKIZUMAB
Product Specifications
Dosage FormSolution
Route of AdministrationSubcutaneous
AHFS Classification84:06.28
Health Canada Classification

ACTIVE INGREDIENTS (1)

BIMEKIZUMABActive
Strength: 320 MG / 2 ML
Monograph: BIMEKIZUMAB

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