Kesimpta

Kesimpta is a medicine authorised by Swissmedic under authorisation number 67757. The authorisation holder is Novartis Pharma Schweiz AG. The medicinal product code is Biotechnological 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 01 February 2021 and the authorisation is valid without a time limit. The export lists no ATC code for this medicine.

  • Dispensing category B
  • Authorisation number 67757
  • Biotechnological medicines
Authorisation data
Authorisation number67757
NameKesimpta
Full nameKesimpta, Injektionslösung in Fertigspritze
Authorisation holderNovartis Pharma Schweiz AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codenot stated
First authorisation01 February 2021
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Kesimpta, Injektionslösung in FertigspritzeB01 February 2021

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing 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 Kesimpta authorised in Switzerland?

Yes. Kesimpta is authorised by Swissmedic under authorisation number 67757, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Kesimpta have?

Kesimpta 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 Kesimpta?

The authorisation holder is Novartis Pharma Schweiz 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.

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