Discontinuation report ACT DUTASTERIDE
| Report ID | 258580 |
| Drug Identification Number | 02412691 |
| Brand name | ACT DUTASTERIDE |
| Common or Proper name | ACT DUTASTERIDE |
| Company Name | TEVA CANADA LIMITED |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | DUTASTERIDE |
| Strength(s) | 0.5MG |
| Dosage form(s) | CAPSULE |
| Route of administration | ORAL ORAL |
| Packaging size | 100, 30 |
| ATC code | G04CB |
| ATC description | DRUGS USED IN BENIGN PROSTATIC HYPERTROPHY |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2019-05-01 |
| Remaining supply date | 2019-05-01 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 30 NOVOPHARM COURT TORONTO, ONTARIO CANADA M1B 2K9 |
| Company contact information |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v2 | 2025-05-28 | French | Compare |
| v1 | 2025-05-28 | English | Compare |
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