Tecartus

Tecartus is a medicine authorised by Swissmedic under authorisation number 67884. The authorisation holder is Gilead Sciences Switzerland Sàrl. The medicinal product code is Transplant: gene therapy product 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 25 August 2021 and the authorisation is valid without a time limit. ATC code L01XL06 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 67884
  • ATC L01XL06
  • Transplant: gene therapy product
Authorisation data
Authorisation number67884
NameTecartus
Full nameTecartus, Infusionsdispersion
Authorisation holderGilead Sciences Switzerland Sàrl
Medicinal product codeTransplant: gene therapy product
Dispensing categoryA · Prescription, not repeatable
ATC codeL01XL06
First authorisation25 August 2021
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Tecartus, InfusionsdispersionA25 August 2021

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11BeutelL01XL0607.16.4.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Tecartus authorised in Switzerland?

Yes. Tecartus is authorised by Swissmedic under authorisation number 67884, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Tecartus have?

Tecartus 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 Tecartus?

The authorisation holder is Gilead Sciences Switzerland Sàrl. 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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