Discontinuation report SODIUM AUROTHIOMALATE INJECTION BP
| Report ID | 55768 |
| Drug Identification Number | 02245458 |
| Brand name | SODIUM AUROTHIOMALATE INJECTION BP |
| Common or Proper name | AUROTHIOMALATE |
| Company Name | SANDOZ CANADA INCORPORATED |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | GOLD SODIUM THIOMALATE |
| Strength(s) | 50MG |
| Dosage form(s) | SOLUTION |
| Route of administration | INTRAMUSCULAR |
| Packaging size | 10 VIALS |
| ATC code | M01CB |
| ATC description | SPECIFIC ANTIRHEUMATIC AGENTS |
| Reason for discontinuation | Raw material availability |
| Anticipated discontinuation date | 2016-08-31 |
| Actual discontinuation date | 2016-09-10 |
| Remaining supply date | 2016-09-10 |
| 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 | |
|---|---|---|---|
| v1 | 2018-07-13 | English | Compare |
| v2 | 2018-07-13 | French | Compare |
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