OPDIVO SC DIN 02557320
Status: Marketed
Holder: BRISTOL-MYERS SQUIBB CANADA
Health Canada record
| Active ingredient(s) | NIVOLUMAB 120 MG |
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| Dosage form | Solution |
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| Route | Subcutaneous |
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| Schedule | PRESCRIPTION; SCHEDULE D |
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| Class | Human |
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| ATC | L01FF01 NIVOLUMAB |
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| Original market date | 30-Dec-2025 |
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| Current status date | 30-Dec-2025 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Bristol-Myers Squibb Canada — licence 100100, currently licensed, last inspection rating C (2026-03-18).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing NIVOLUMAB
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02446626 | OPDIVO | BRISTOL-MYERS SQUIBB CANADA | Solution | NIVOLUMAB 10 MG | Marketed |
| 02446634 | OPDIVO | BRISTOL-MYERS SQUIBB CANADA | Solution | NIVOLUMAB 10 MG | Marketed |
| 02566931 | OPDIVO SC | BRISTOL-MYERS SQUIBB CANADA | Solution | NIVOLUMAB 120 MG | Approved |
| 02541416 | OPDUALAG | BRISTOL-MYERS SQUIBB CANADA | Solution | NIVOLUMAB 240 MG; RELATLIMAB 80 MG | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 35291 | 2025-05-01 | Supplement to a New Drug Submission (SNDS) | New formulation. New route of administration |
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