Drug · DIN 00788805
HEXABRIX 200
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since July 8, 2015; first marketed December 31, 1988.
- Drug Identification Number (DIN)
- 00788805
- Company (DIN owner)
- GuerbetRoissy Cdg Cedex, Val-D'Oise, France
- Schedule
- Ethical
- Dosage form
- Solution
- Route
- Intravascular
- Therapeutic class (ATC)
- Ioxaglic acid V08AB03
- Class
- Human
- Record last updated
- June 18, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| IOXAGLATE SODIUM | 123 MG | ML |
| IOXAGLATE MEGLUMINE | 246 MG | ML |
Notices of Compliance
Health Canada approvals that name this DIN.
- May 6, 2013: NOC 14339New Drug Submission (NDS) · Manufacturer name change
- January 22, 2003: NOC 1500New Drug Submission (NDS) · Manufacturer name change