Sugammadex Viatris 200 mg/ 2 ml
Sugammadex Viatris 200 mg/ 2 ml is a medicine authorised by Swissmedic under authorisation number 69530. The authorisation holder is Viatris Pharma GmbH. 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 09 July 2024 and the authorisation is limited until 08 July 2029. ATC code V03AB35 places the medicine in the group All other therapeutic products.
| Authorisation number | 69530 |
|---|---|
| Name | Sugammadex Viatris 200 mg/ 2 ml |
| Full name | Sugammadex Viatris 200 mg/ 2 ml, Injektionslösung |
| Authorisation holder | Viatris Pharma GmbH |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | V03AB35 |
| First authorisation | 09 July 2024 |
| Authorisation validity | 08 July 2029 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Sugammadex Viatris 200 mg/ 2 ml, Injektionslösung | B | 09 July 2024 |
| 2 | Sugammadex Viatris 500 mg/ 5 ml, Injektionslösung | B | 09 July 2024 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 10 | Durchstechflasche(n) | V03AB35 | 15.01.0. | B |
| 2 | 10 | Durchstechflasche(n) | V03AB35 | 15.01.0. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Sugammadex Viatris 200 mg/ 2 ml authorised in Switzerland?
Yes. Sugammadex Viatris 200 mg/ 2 ml is authorised by Swissmedic under authorisation number 69530, data as of 01 September 2026. The authorisation is limited until 08 July 2029.
Which dispensing category does Sugammadex Viatris 200 mg/ 2 ml have?
Sugammadex Viatris 200 mg/ 2 ml 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 Sugammadex Viatris 200 mg/ 2 ml?
The authorisation holder is Viatris Pharma GmbH. 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.