LUCENTIS DIN 02425629
Health Canada record
| Active ingredient(s) | RANIBIZUMAB 10 MG |
|---|---|
| Dosage form | Solution |
| Route | Intravitreal |
| Schedule | PRESCRIPTION; SCHEDULE D |
| Class | Human |
| ATC | S01LA04 RANIBIZUMAB |
| Original market date | 18-Sep-2014 |
| Current status date | 18-Sep-2014 |
| 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 RANIBIZUMAB
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02296810 | LUCENTIS | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | RANIBIZUMAB 10 MG | Marketed |
| 02525852 | MELVIZO | SAMSUNG BIOEPIS CO., LTD | Solution | RANIBIZUMAB 10 MG | Marketed |
| 02542250 | RANOPTO | TEVA CANADA LIMITED | Solution | RANIBIZUMAB 10 MG | Marketed |
| 02568942 | RANVU | APOTEX INC | Solution | RANIBIZUMAB 10 MG | Approved |
| 02568950 | RANVU | APOTEX INC | Solution | RANIBIZUMAB 10 MG | Approved |
| 02530589 | SUSVIMO | HOFFMANN-LA ROCHE LIMITED | Solution | RANIBIZUMAB 100 MG | Approved |