Micardis Plus 80/12
Micardis Plus 80/12 is a medicine authorised by Swissmedic under authorisation number 55970. The authorisation holder is Boehringer Ingelheim (Schweiz) 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 30 August 2002 and the authorisation is valid without a time limit. ATC code C09DA07 places the medicine in the group Agents acting on the renin-angiotensin system.
| Authorisation number | 55970 |
|---|---|
| Name | Micardis Plus 80/12 |
| Full name | Micardis Plus 80/12,5 mg, Tabletten |
| Authorisation holder | Boehringer Ingelheim (Schweiz) GmbH |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | C09DA07 |
| First authorisation | 30 August 2002 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 2 | Micardis Plus 80/12,5 mg, Tabletten | B | 30 August 2002 |
| 3 | Micardis Plus 80/25 mg, Tabletten | B | 06 March 2008 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 5 | 28 | Tablette(n) | C09DA07 | 02.07.2. | B |
| 7 | 98 | Tablette(n) | C09DA07 | 02.07.2. | B |
| 9 | 28 | Tablette(n) | C09DA07 | 02.07.2. | B |
| 11 | 98 | Tablette(n) | C09DA07 | 02.07.2. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Micardis Plus 80/12 authorised in Switzerland?
Yes. Micardis Plus 80/12 is authorised by Swissmedic under authorisation number 55970, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Micardis Plus 80/12 have?
Micardis Plus 80/12 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 Micardis Plus 80/12?
The authorisation holder is Boehringer Ingelheim (Schweiz) 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.