Alyftrek 4 mg/ 20 mg/ 50 mg
Alyftrek 4 mg/ 20 mg/ 50 mg is a medicine authorised by Swissmedic under authorisation number 69398. The authorisation holder is Vertex Pharmaceuticals (CH) GmbH. The medicinal product code is Synthetic 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 15 October 2025 and the authorisation is limited until 14 October 2030. ATC code R07AX33 places the medicine in the group Other respiratory system products.
| Authorisation number | 69398 |
|---|---|
| Name | Alyftrek 4 mg/ 20 mg/ 50 mg |
| Full name | Alyftrek 4 mg/ 20 mg/ 50 mg, Filmtabletten |
| Authorisation holder | Vertex Pharmaceuticals (CH) GmbH |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | R07AX33 |
| First authorisation | 15 October 2025 |
| Authorisation validity | 14 October 2030 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Alyftrek 4 mg/ 20 mg/ 50 mg, Filmtabletten | A | 15 October 2025 |
| 2 | Alyftrek 10 mg/ 50 mg/ 125 mg, Filmtabletten | A | 15 October 2025 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 84 | Tablette(n) | R07AX33 | 03.99.0. | A |
| 2 | 56 | Tablette(n) | R07AX33 | 03.99.0. | A |
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Other medicines from this authorisation holder
Frequently asked questions
Is Alyftrek 4 mg/ 20 mg/ 50 mg authorised in Switzerland?
Yes. Alyftrek 4 mg/ 20 mg/ 50 mg is authorised by Swissmedic under authorisation number 69398, data as of 01 September 2026. The authorisation is limited until 14 October 2030.
Which dispensing category does Alyftrek 4 mg/ 20 mg/ 50 mg have?
Alyftrek 4 mg/ 20 mg/ 50 mg 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 Alyftrek 4 mg/ 20 mg/ 50 mg?
The authorisation holder is Vertex Pharmaceuticals (CH) 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.