Orthoton 750 mg
Orthoton 750 mg is a medicine authorised by Swissmedic under authorisation number 68326. The authorisation holder is RECORDATI 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 20 July 2023 and the authorisation is limited until 19 July 2028. The export lists no ATC code for this medicine.
| Authorisation number | 68326 |
|---|---|
| Name | Orthoton 750 mg |
| Full name | Orthoton 750 mg, Filmtabletten |
| Authorisation holder | RECORDATI AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | not stated |
| First authorisation | 20 July 2023 |
| Authorisation validity | 19 July 2028 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Orthoton 750 mg, Filmtabletten | B | 20 July 2023 |
| 2 | Orthoton 1500 mg, Filmtabletten | B | 20 July 2023 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| The Swissmedic export lists no pack sizes for this medicine. | |||||
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Other medicines from this authorisation holder
Frequently asked questions
Is Orthoton 750 mg authorised in Switzerland?
Yes. Orthoton 750 mg is authorised by Swissmedic under authorisation number 68326, data as of 01 September 2026. The authorisation is limited until 19 July 2028.
Which dispensing category does Orthoton 750 mg have?
Orthoton 750 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 Orthoton 750 mg?
The authorisation holder is RECORDATI 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.