SKYRIZI DIN 02572850
Health Canada record
| Active ingredient(s) | RISANKIZUMAB 55 MG |
|---|---|
| Dosage form | Solution |
| Route | Subcutaneous |
| Schedule | SCHEDULE D; PRESCRIPTION |
| Class | Human |
| ATC | L04AC18 RIZANKIZUMAB |
| Original market date | |
| Current status date | 16-Oct-2026 |
| Source | Health Canada DPD |
Establishment licence of the holder
AbbVie Corporation — licence 101988, currently licensed, last inspection rating C (2023-07-18).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing RISANKIZUMAB
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02532093 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 360 MG | Marketed |
| 02519291 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 150 MG | Marketed |
| 02519283 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 150 MG | Marketed |
| 02546922 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 90 MG | Approved |
| 02532107 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 60 MG | Marketed |
| 02552507 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 180 MG | Marketed |
| 02487454 | SKYRIZI | ABBVIE CORPORATION | Solution | RISANKIZUMAB 75 MG | Cancelled Post Market |