Ivabradin Viatris 5 mg
Ivabradin Viatris 5 mg is a medicine authorised by Swissmedic under authorisation number 67253. 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 31 July 2019 and the authorisation is valid without a time limit. ATC code C01EB17 places the medicine in the group Cardiac therapy.
| Authorisation number | 67253 |
|---|---|
| Name | Ivabradin Viatris 5 mg |
| Full name | Ivabradin Viatris 5 mg, Filmtabletten |
| Authorisation holder | Viatris Pharma GmbH |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | C01EB17 |
| First authorisation | 31 July 2019 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Ivabradin Viatris 5 mg, Filmtabletten | B | 31 July 2019 |
| 2 | Ivabradin Viatris 7.5 mg, Filmtabletten | B | 31 July 2019 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 5 | 56 | Tablette(n) | C01EB17 | 02.99.0. | B |
| 6 | 112 | Tablette(n) | C01EB17 | 02.99.0. | B |
| 7 | 56 | Tablette(n) | C01EB17 | 02.99.0. | B |
| 8 | 112 | Tablette(n) | C01EB17 | 02.99.0. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Ivabradin Viatris 5 mg authorised in Switzerland?
Yes. Ivabradin Viatris 5 mg is authorised by Swissmedic under authorisation number 67253, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Ivabradin Viatris 5 mg have?
Ivabradin Viatris 5 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 Ivabradin Viatris 5 mg?
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.