Discontinuation report ULTRAVIST 240
| Report ID | 81959 |
| Drug Identification Number | 02078597 |
| Brand name | ULTRAVIST 240 |
| Common or Proper name | Iopromide |
| Company Name | BAYER INC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | IOPROMIDE |
| Strength(s) | 50% |
| Dosage form(s) | SOLUTION |
| Route of administration | INTRAVASCULAR |
| Packaging size | 50 & 200ML |
| ATC code | V08AB |
| ATC description | X-RAY CONTRAST MEDIA, IODINATED |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2019-04-16 |
| Actual discontinuation date | 2019-04-16 |
| Remaining supply date | 2019-04-30 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 2920 MATHESON BLVD EAST MISSISSAUGA, ONTARIO CANADA L4W 5R6 |
| Company contact information | 1-800-265-7382 |
Version History
Click on "Compare" below to view the full report history and compare to other versions.
| Version Number | Date Updated | Language | |
|---|---|---|---|
| v2 | 2019-04-17 | French | Compare |
| v1 | 2019-04-17 | English | Compare |
Showing 1 to 2 of 2