MedPath

ACTEMRA

ACTEMRA

Approved
DIN Number

02483327

Drug Class

Human

Market Date

Jan 15, 2019

Company
HC

Hoffmann-La Roche Limited

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 Number02483327
AIG Number0152713002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D ,  Prescription
A
ATC Code
L04AC07 TOCILIZUMAB
Product Specifications
Dosage FormSolution
Route of AdministrationSubcutaneous
AHFS Classification90:24.20.92
Health Canada Classification

ACTIVE INGREDIENTS (1)

TOCILIZUMABActive
Strength: 162 MG / 0.9 ML
Monograph: TOCILIZUMAB

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