JAKAVI DIN 02388022
Status: Marketed
Holder: NOVARTIS PHARMACEUTICALS CANADA INC
Molecule: RUXOLITINIB (RUXOLITINIB PHOSPHATE)
Available to quote
Health Canada record
| Active ingredient(s) | RUXOLITINIB (RUXOLITINIB PHOSPHATE) 20 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | L01EJ01 RUXOLITINIB |
| Original market date | 19-Jul-2012 |
| Current status date | 19-Jul-2012 |
| Source | Health Canada DPD |
Establishment licence of the holder
Novartis Pharmaceuticals Canada Inc — licence 100273, currently licensed, last inspection rating C (2025-01-14).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing RUXOLITINIB (RUXOLITINIB PHOSPHATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02388006 | JAKAVI | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | RUXOLITINIB (RUXOLITINIB PHOSPHATE) 5 MG | Marketed |
| 02388014 | JAKAVI | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | RUXOLITINIB (RUXOLITINIB PHOSPHATE) 15 MG | Marketed |
| 02434814 | JAKAVI | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | RUXOLITINIB (RUXOLITINIB PHOSPHATE) 10 MG | Marketed |
| 02552434 | OPZELURA | INCYTE CORPORATION | Cream | RUXOLITINIB (RUXOLITINIB PHOSPHATE) 1.5 % | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 13404 | 2012-06-19 | New Drug Submission (NDS) |