LUCENTIS DIN 02296810
Status: Marketed
Holder: NOVARTIS PHARMACEUTICALS CANADA INC
Health Canada record
| Active ingredient(s) | RANIBIZUMAB 10 MG |
|---|
| Dosage form | Solution |
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| Route | Intravitreal |
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| Schedule | PRESCRIPTION; SCHEDULE D |
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| Class | Human |
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| ATC | S01LA04 RANIBIZUMAB |
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| Original market date | 26-Jul-2007 |
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| Current status date | 29-May-2014 |
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| Source | Health Canada DPD |
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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 |
|---|
| 02425629 | 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 |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 15653 | 2014-05-28 | Supplement to a New Drug Submission (SNDS) | NEW PRESENTATION |
| 9528 | 2008-04-30 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 8866 | 2007-06-26 | New Drug Submission (NDS) | |
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