Kenacort-A Solubile 10 mg/0.25 mL
Kenacort-A Solubile 10 mg/0.25 mL is a medicine authorised by Swissmedic under authorisation number 38774. The authorisation holder is Dermapharm 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 02 September 1975 and the authorisation is valid without a time limit. ATC code H02AB08 places the medicine in the group Corticosteroids for systemic use.
| Authorisation number | 38774 |
|---|---|
| Name | Kenacort-A Solubile 10 mg/0.25 mL |
| Full name | Kenacort-A Solubile 10 mg/0.25 mL, Injektionslösung |
| Authorisation holder | Dermapharm AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | H02AB08 |
| First authorisation | 02 September 1975 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 8 | Kenacort-A Solubile 10 mg/0.25 mL, Injektionslösung | B | 11 June 2012 |
| 9 | Kenacort-A Solubile 40 mg/1 mL, Injektionslösung | B | 11 June 2012 |
| 10 | Kenacort-A Solubile 80 mg/2 mL, Injektionslösung | B | 11 June 2012 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 213 | 5 | Ampulle(n) | H02AB08 | 07.07.24 | B |
| 214 | 5 | Ampulle(n) | H02AB08 | 07.07.24 | B |
| 215 | 5 | Ampulle(n) | H02AB08 | 07.07.24 | B |
| 216 | 1 | Spritze(n) | H02AB08 | 07.07.24 | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Kenacort-A Solubile 10 mg/0.25 mL authorised in Switzerland?
Yes. Kenacort-A Solubile 10 mg/0.25 mL is authorised by Swissmedic under authorisation number 38774, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Kenacort-A Solubile 10 mg/0.25 mL have?
Kenacort-A Solubile 10 mg/0.25 mL 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 Kenacort-A Solubile 10 mg/0.25 mL?
The authorisation holder is Dermapharm 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.