Dexilant 30 mg
Dexilant 30 mg is a medicine authorised by Swissmedic under authorisation number 62993. The authorisation holder is Takeda Pharma 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 09 May 2014 and the authorisation is valid without a time limit. ATC code A02BC06 places the medicine in the group Drugs for acid related disorders.
| Authorisation number | 62993 |
|---|---|
| Name | Dexilant 30 mg |
| Full name | Dexilant 30 mg, Hartkapseln mit veränderter Wirkstofffreisetzung |
| Authorisation holder | Takeda Pharma AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | A02BC06 |
| First authorisation | 09 May 2014 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Dexilant 30 mg, Hartkapseln mit veränderter Wirkstofffreisetzung | B | 09 May 2014 |
| 2 | Dexilant 60 mg, Hartkapseln mit veränderter Wirkstofffreisetzung | B | 09 May 2014 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 14 | Kapsel(n) | A02BC06 | 04.99.0. | B |
| 2 | 28 | Kapsel(n) | A02BC06 | 04.99.0. | B |
| 5 | 98 | Kapsel(n) | A02BC06 | 04.99.0. | B |
| 3 | 14 | Kapsel(n) | A02BC06 | 04.99.0. | B |
| 4 | 28 | Kapsel(n) | A02BC06 | 04.99.0. | B |
| 6 | 56 | Kapsel(n) | A02BC06 | 04.99.0. | B |
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Frequently asked questions
Is Dexilant 30 mg authorised in Switzerland?
Yes. Dexilant 30 mg is authorised by Swissmedic under authorisation number 62993, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Dexilant 30 mg have?
Dexilant 30 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 Dexilant 30 mg?
The authorisation holder is Takeda Pharma 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.