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The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2010-05-26

Original market date: See footnote 1

2010-05-26

Product name:

ACTEMRA

Description:

4 SINGLE USE VIALS. PRESERVATIVE-FREE

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section .

DIN:

02350106

Product Monograph/Veterinary Labelling:

Date: 2021-01-04 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

HOFFMANN-LA ROCHE LIMITED
7070 Mississauga Road
Mississauga
Ontario
Canada  L5N 5M8

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

1

Schedule(s):

Schedule D,  Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

92:36.00   DISEASE-MODIFYING ANTIRHEUMATIC AGENTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

L04AC07  TOCILIZUMAB

Active ingredient group (AIG) number:See footnote 5

0152713001

List of active ingredient(s)
Active ingredient(s) Strength
TOCILIZUMAB 200 MG / 10 ML

Risk Management Plans See footnote 7

A Risk Management Plan (RMP) for this product was submitted.

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