Discontinuation report GLYBURIDE
| Report ID | 230704 |
| Drug Identification Number | 02485664 |
| Brand name | GLYBURIDE |
| Common or Proper name | GLYBURIDE |
| Company Name | PRO DOC LIMITEE |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | GLYBURIDE |
| Strength(s) | 5MG |
| Dosage form(s) | TABLET |
| Route of administration | ORAL ORAL |
| Packaging size | 500 |
| ATC code | A10BB |
| ATC description | BLOOD GLUCOSE LOWERING DRUGS, EXCL. INSULINS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2024-12-31 |
| Actual discontinuation date | 2024-06-17 |
| Remaining supply date | 2025-04-30 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 2925 BOULEVARD INDUSTRIEL LAVAL, QUEBEC CANADA H7L 3W9 |
| Company contact information | 2925 BOULEVARD INDUSTRIEL, LAVAL QC, H7L 3W9 |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v4 | 2024-06-27 | French | Compare |
| v3 | 2024-06-27 | English | Compare |
| v2 | 2024-06-17 | French | Compare |
| v1 | 2024-06-17 | English | Compare |
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