Xeomin 50 LD50-Einheiten
Xeomin 50 LD50-Einheiten is a medicine authorised by Swissmedic under authorisation number 62080. The authorisation holder is Merz Pharma (Schweiz) AG. The medicinal product code is Biotechnological medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 12 April 2013 and the authorisation is valid without a time limit. ATC code M03AX01 places the medicine in the group Muscle relaxants.
| Authorisation number | 62080 |
|---|---|
| Name | Xeomin 50 LD50-Einheiten |
| Full name | Xeomin 50 LD50-Einheiten, Pulver zur Herstellung einer Injektionslösung |
| Authorisation holder | Merz Pharma (Schweiz) AG |
| Medicinal product code | Biotechnological medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | M03AX01 |
| First authorisation | 12 April 2013 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Xeomin 50 LD50-Einheiten, Pulver zur Herstellung einer Injektionslösung | A | 12 April 2013 |
| 2 | Xeomin 100 LD50-Einheiten, Pulver zur Herstellung einer Injektionslösung | A | 12 April 2013 |
| 3 | Xeomin 200 LD50-Einheiten, Pulver zur Herstellung einer Injektionslösung | A | 24 August 2020 |
Scroll the table sideways
| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 1 | Durchstechflasche(n) | M03AX01 | 01.13.0. | A |
| 2 | 1 | Durchstechflasche(n) | M03AX01 | 01.13.0. | A |
| 3 | 1 | Durchstechflasche(n) | M03AX01 | 01.13.0. | A |
Scroll the table sideways
Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Xeomin 50 LD50-Einheiten authorised in Switzerland?
Yes. Xeomin 50 LD50-Einheiten is authorised by Swissmedic under authorisation number 62080, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Xeomin 50 LD50-Einheiten have?
Xeomin 50 LD50-Einheiten is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.
Who is the authorisation holder of Xeomin 50 LD50-Einheiten?
The authorisation holder is Merz Pharma (Schweiz) 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.