Drug Report History #257747
Below you will find the report version history. When a report is updated, a new version of the report is created. The report history allows you to see the changes between versions. You can select two versions of the report to compare. The fields that have changed between versions will be highlighted in yellow, and the changes will be clearly marked as updated.
The translation of reports creates two separate versions which is why some reports may not seem to have any differences. In this case, only the language field below will be highlighted in yellow, and the change will be clearly marked as updated.
| Field | Version v3-EN | Version v2-FR |
|---|---|---|
| Language | English (Updated) | French |
| Date Updated | 2025-11-20 (Updated) | 2025-11-19 |
| Drug Identification Number | 02482622 | 02482622 |
| Brand name | APO-TICAGRELOR | APO-TICAGRELOR |
| Common or Proper name | Nom commun ou nom propre | Nom commun ou nom propre |
| Company Name | APOTEX INC | APOTEX INC |
| Ingredients | TICAGRELOR | TICAGRELOR |
| Strength(s) | 60MG | 60MG |
| Dosage form(s) | TABLET | TABLET |
| Route of administration | ORAL | ORAL |
| Packaging size | Taille de l’emballage | Taille de l’emballage |
| ATC code | B01AC | B01AC |
| ATC description | ANTITHROMBOTIC AGENTS | ANTITHROMBOTIC AGENTS |
| Reason for discontinuation | Raw material availability | Raw material availability |
| Anticipated discontinuation date | 2022-01-02 | 2022-01-02 |
| Actual discontinuation date | 2024-08-17 | 2024-08-17 |
| Remaining supply date | ||
| Discontinuation status | Discontinued | Discontinued |
| Discontinuation decision reversal | No | No |
| Tier 3 Status | Yes (Updated) | No |
| Information on remaining supply | ||
| Company comments | ||
| Health Canada comments |