Discontinuation report HEPARIN SODIUM INJECTION USP (MULTIDOSE VIAL-WITH PRESERVATIVE)
| Report ID | 228249 |
| Drug Identification Number | 02303108 |
| Brand name | HEPARIN SODIUM INJECTION USP (MULTIDOSE VIAL-WITH PRESERVATIVE) |
| Common or Proper name | HEPARIN NA |
| Company Name | SANDOZ CANADA INCORPORATED |
| Market Status | MARKETED |
| Active Ingredient(s) | HEPARIN SODIUM |
| Strength(s) | 10000UNIT |
| Dosage form(s) | SOLUTION |
| Route of administration | SUBCUTANEOUS INTRAVENOUS SUBCUTANEOUS INTRAVENOUS |
| Packaging size | 50ML 1LIVI |
| ATC code | B01AB |
| ATC description | ANTITHROMBOTIC AGENTS |
| Reason for discontinuation | Manufacturing issues |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2024-05-17 |
| Remaining supply date | 2024-05-17 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 110 RUE DE LAUZON BOUCHERVILLE, QUEBEC CANADA J4B 1E6 |
| Company contact information | 1 800-361-3062 |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v3 | 2024-05-18 | English | Compare |
| v2 | 2024-05-17 | French | Compare |
| v1 | 2024-05-17 | English | Compare |
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