Kerendia 10 mg
Kerendia 10 mg is a medicine authorised by Swissmedic under authorisation number 68130. The authorisation holder is Bayer (Schweiz) 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 26 November 2021 and the authorisation is valid without a time limit. ATC code C03DA05 places the medicine in the group Diuretics.
| Authorisation number | 68130 |
|---|---|
| Name | Kerendia 10 mg |
| Full name | Kerendia 10 mg, Filmtabletten |
| Authorisation holder | Bayer (Schweiz) AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | C03DA05 |
| First authorisation | 26 November 2021 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Kerendia 10 mg, Filmtabletten | B | 26 November 2021 |
| 2 | Kerendia 20 mg, Filmtabletten | B | 26 November 2021 |
| 3 | Kerendia 40 mg, Filmtabletten | B | 09 January 2026 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 28 | Tablette(n) | C03DA05 | 07.09.0. | B |
| 2 | 98 | Tablette(n) | C03DA05 | 07.09.0. | B |
| 4 | 28 | Tablette(n) | C03DA05 | 07.09.0. | B |
| 5 | 98 | Tablette(n) | C03DA05 | 07.09.0. | B |
| 7 | 28 | Tablette(n) | C03DA05 | 07.09.0. | B |
| 8 | 98 | Tablette(n) | C03DA05 | 07.09.0. | B |
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Frequently asked questions
Is Kerendia 10 mg authorised in Switzerland?
Yes. Kerendia 10 mg is authorised by Swissmedic under authorisation number 68130, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Kerendia 10 mg have?
Kerendia 10 mg 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 Kerendia 10 mg?
The authorisation holder is Bayer (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.