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
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Version Number | Date Updated | Language | |
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v2 | 2019-04-17 | French | Compare |
v1 | 2019-04-17 | English | Compare |
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