Discontinuation report CABLIVI
| Report ID | 248053 |
| Drug Identification Number | 02496194 |
| Brand name | CABLIVI |
| Common or Proper name | CAPLACIZUMAB |
| Company Name | SANOFI-AVENTIS CANADA INC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | CAPLACIZUMAB |
| Strength(s) | 11MG |
| Dosage form(s) | POWDER FOR SOLUTION KIT |
| Route of administration | SUBCUTANEOUS INTRAVENOUS |
|
Packaging sizes (GTIN)
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| Additional packaging sizes | 1 vial/box |
| ATC code | B01AX |
| ATC description | |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2025-01-14 |
| Actual discontinuation date | 2025-01-14 |
| Remaining supply date | |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Company contact information | email: [email protected] Telephone: 1-800-265-7927 |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v4 | 2025-01-17 | French | Compare |
| v3 | 2025-01-17 | English | Compare |
| v2 | 2025-01-17 | French | Compare |
| v1 | 2025-01-17 | English | Compare |
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