Discontinuation report ACT DILTIAZEM CD
| Report ID | 81418 |
| Drug Identification Number | 02370638 |
| Brand name | ACT DILTIAZEM CD |
| Common or Proper name | DILTIAZEM CD |
| Company Name | TEVA CANADA LIMITED |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | DILTIAZEM HYDROCHLORIDE |
| Strength(s) | 180MG |
| Dosage form(s) | CAPSULE (EXTENDED RELEASE) |
| Route of administration | ORAL |
| Packaging size | 500 |
| ATC code | C08DB |
| ATC description | SELECTIVE CALC.CHANNEL BLOCK. W/DIRECT CARDIAC EFF |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2019-03-15 |
| Remaining supply date | 2019-05-30 |
| 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
Click on "Compare" below to view the full report history and compare to other versions.
| Version Number | Date Updated | Language | |
|---|---|---|---|
| v2 | 2019-04-11 | French | Compare |
| v1 | 2019-04-11 | English | Compare |
Showing 1 to 2 of 2