Product information
From Health Canada
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:
Approved
Current status date:
2018-03-26
Product name:
HUMIRA
Description:
PREFILLED SYRINGE
DIN:
02474255
Product Monograph/Veterinary Labelling:
Date:
2022-09-16
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
ABBVIE CORPORATION
8401 Trans-Canada Highway
Saint-Laurent
Quebec
Canada
H4S 1Z1
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Subcutaneous
Number of active ingredient(s):
1
Schedule(s):
Schedule D , Prescription
American Hospital Formulary Service (AHFS): See footnote 3
92:36.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
L04AB04 ADALIMUMAB
Active ingredient group (AIG) number:See footnote5
0150364002
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| ADALIMUMAB | 10 MG / 0.1 ML |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
| Additional Risk Minimization Measures |
|---|
| Patient Wallet Card |
| Pharmacovigilance/Monitoring Activity |
|---|
| Clinical Trials |
| Observational Studies |
| Registry |