Fabhalta 200 mg

Fabhalta 200 mg is a medicine authorised by Swissmedic under authorisation number 68603. The authorisation holder is Novartis Pharma Schweiz AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 29 August 2024 and the authorisation is limited until 28 August 2029. ATC code L04AJ08 places the medicine in the group Immunosuppressants.

  • Dispensing category A
  • Authorisation number 68603
  • ATC L04AJ08
  • Synthetic medicines
Authorisation data
Authorisation number68603
NameFabhalta 200 mg
Full nameFabhalta 200 mg, Hartkapseln
Authorisation holderNovartis Pharma Schweiz AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL04AJ08
First authorisation29 August 2024
Authorisation validity28 August 2029
Strengths
No.NameDispensing categoryAuthorisation date
1Fabhalta 200 mg, HartkapselnA29 August 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
156Kapsel(n)L04AJ0807.15.0.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Fabhalta 200 mg authorised in Switzerland?

Yes. Fabhalta 200 mg is authorised by Swissmedic under authorisation number 68603, data as of 01 September 2026. The authorisation is limited until 28 August 2029.

Which dispensing category does Fabhalta 200 mg have?

Fabhalta 200 mg is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.

Who is the authorisation holder of Fabhalta 200 mg?

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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