Discontinuation report ACT NABILONE
| Report ID | 97581 |
| Drug Identification Number | 02393603 |
| Brand name | ACT NABILONE |
| Common or Proper name | NABILONE 1MG CAPSULES |
| Company Name | TEVA CANADA LIMITED |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | NABILONE |
| Strength(s) | 1MG |
| Dosage form(s) | CAPSULE |
| Route of administration | ORAL |
| Packaging size | 50's &100's |
| ATC code | A04AD |
| ATC description | ANTIEMETICS AND ANTINAUSEANTS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2019-10-31 |
| Actual discontinuation date | 2019-10-31 |
| Remaining supply date | 2019-10-31 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | ACT Product is discontinued and is transitioning to the TEVA DIN |
| 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 | |
|---|---|---|---|
| v3 | 2019-11-01 | English | Compare |
| v2 | 2019-10-31 | French | Compare |
| v1 | 2019-10-31 | English | Compare |
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