RANOPTO DIN 02542250
Status: Marketed
Holder: TEVA CANADA LIMITED
Available to quote
Health Canada record
| Active ingredient(s) | RANIBIZUMAB 10 MG |
|---|
| Dosage form | Solution |
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| Route | Intravitreal |
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| Schedule | SCHEDULE D; PRESCRIPTION |
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| Class | Human |
|---|
| ATC | S01LA04 RANIBIZUMAB |
|---|
| Original market date | 26-Feb-2024 |
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| Current status date | 26-Feb-2024 |
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| Source | Health Canada DPD |
|---|
Establishment licence of the holder
Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).
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 |
| 02425629 | LUCENTIS | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | RANIBIZUMAB 10 MG | Marketed |
| 02525852 | MELVIZO | SAMSUNG BIOEPIS CO., LTD | 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 |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 31825 | 2023-10-11 | New Drug Submission (NDS) | |
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