Ospolot 20 mg/ml

Ospolot 20 mg/ml is a medicine authorised by Swissmedic under authorisation number 69828. The authorisation holder is Desitin Pharma 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 05 August 2025 and the authorisation is limited until 04 August 2030. ATC code N03AX03 places the medicine in the group Antiepileptics.

  • Dispensing category B
  • Authorisation number 69828
  • ATC N03AX03
  • Synthetic medicines
Authorisation data
Authorisation number69828
NameOspolot 20 mg/ml
Full nameOspolot 20 mg/ml, Suspension zum Einnehmen
Authorisation holderDesitin Pharma GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN03AX03
First authorisation05 August 2025
Authorisation validity04 August 2030
Strengths
No.NameDispensing categoryAuthorisation date
1Ospolot 20 mg/ml, Suspension zum EinnehmenB05 August 2025

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1250mlN03AX0301.07.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ospolot 20 mg/ml authorised in Switzerland?

Yes. Ospolot 20 mg/ml is authorised by Swissmedic under authorisation number 69828, data as of 01 September 2026. The authorisation is limited until 04 August 2030.

Which dispensing category does Ospolot 20 mg/ml have?

Ospolot 20 mg/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 Ospolot 20 mg/ml?

The authorisation holder is Desitin Pharma 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.

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