Lipiodol Ultra-fluide
Lipiodol Ultra-fluide is a medicine authorised by Swissmedic under authorisation number 30274. The authorisation holder is Guerbet AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 24 September 1964 and the authorisation is valid without a time limit. ATC code V08AD01 places the medicine in the group Contrast media.
| Authorisation number | 30274 |
|---|---|
| Name | Lipiodol Ultra-fluide |
| Full name | Lipiodol Ultra-fluide, Injektionslösung |
| Authorisation holder | Guerbet AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | V08AD01 |
| First authorisation | 24 September 1964 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 2 | Lipiodol Ultra-fluide, Injektionslösung | B | 12 June 2003 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 24 | 1 | Ampulle(n) | V08AD01 | 14.01.0. | B |
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Frequently asked questions
Is Lipiodol Ultra-fluide authorised in Switzerland?
Yes. Lipiodol Ultra-fluide is authorised by Swissmedic under authorisation number 30274, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Lipiodol Ultra-fluide have?
Lipiodol Ultra-fluide is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Lipiodol Ultra-fluide?
The authorisation holder is Guerbet AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.