Discontinuation report TUSSIONEX
| Report ID | 98368 |
| Drug Identification Number | 01916971 |
| Brand name | TUSSIONEX |
| Common or Proper name | Tussionex |
| Company Name | SANOFI-AVENTIS CANADA INC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | HYDROCODONE PHENYLTOLOXAMINE |
| Strength(s) | 5MG 10MG |
| Dosage form(s) | SUSPENSION |
| Route of administration | ORAL |
| Packaging size | 500ml |
| ATC code | R05DA |
| ATC description | COUGH SUPPRESSANTS EXCL. COMB. WITH EXPECTORANTS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2020-01-14 |
| Actual discontinuation date | 2020-02-07 |
| Remaining supply date | 2020-01-31 |
| 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
Click on "Compare" below to view the full report history and compare to other versions.
| Version Number | Date Updated | Language | |
|---|---|---|---|
| v7 | 2020-03-24 | English | Compare |
| v6 | 2020-01-24 | French | Compare |
| v5 | 2020-01-24 | English | Compare |
| v4 | 2019-12-11 | French | Compare |
| v3 | 2019-12-11 | English | Compare |
| v2 | 2019-11-11 | French | Compare |
| v1 | 2019-11-11 | English | Compare |
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