Risperdal Consta 25 mg
Risperdal Consta 25 mg is a medicine authorised by Swissmedic under authorisation number 56092. The authorisation holder is Janssen-Cilag 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 June 2002 and the authorisation is valid without a time limit. ATC code N05AX08 places the medicine in the group Psycholeptics.
| Authorisation number | 56092 |
|---|---|
| Name | Risperdal Consta 25 mg |
| Full name | Risperdal Consta 25 mg, Suspension zur i.m. Applikation |
| Authorisation holder | Janssen-Cilag AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | N05AX08 |
| First authorisation | 26 June 2002 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Risperdal Consta 25 mg, Suspension zur i.m. Applikation | B | 26 June 2002 |
| 2 | Risperdal Consta 37,5 mg, Suspension zur i.m. Applikation | B | 26 June 2002 |
| 3 | Risperdal Consta 50 mg, Suspension zur i.m. Applikation | B | 26 June 2002 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 1 | Set | N05AX08 | 01.05.0. | B |
| 3 | 1 | Set | N05AX08 | 01.05.0. | B |
| 5 | 1 | Set | N05AX08 | 01.05.0. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Risperdal Consta 25 mg authorised in Switzerland?
Yes. Risperdal Consta 25 mg is authorised by Swissmedic under authorisation number 56092, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Risperdal Consta 25 mg have?
Risperdal Consta 25 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 Risperdal Consta 25 mg?
The authorisation holder is Janssen-Cilag 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.