Trikafta 100 mg / 50 mg / 75 mg

Trikafta 100 mg / 50 mg / 75 mg is a medicine authorised by Swissmedic under authorisation number 69212. The authorisation holder is Vertex Pharmaceuticals (CH) GmbH. 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 13 June 2024 and the authorisation is limited until 12 June 2029. ATC code R07AX32 places the medicine in the group Other respiratory system products.

  • Dispensing category A
  • Authorisation number 69212
  • ATC R07AX32
  • Synthetic medicines
Authorisation data
Authorisation number69212
NameTrikafta 100 mg / 50 mg / 75 mg
Full nameTrikafta 100 mg / 50 mg / 75 mg, 75 mg, Granulat
Authorisation holderVertex Pharmaceuticals (CH) GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeR07AX32
First authorisation13 June 2024
Authorisation validity12 June 2029
Strengths
No.NameDispensing categoryAuthorisation date
1Trikafta 100 mg / 50 mg / 75 mg, 75 mg, GranulatA13 June 2024
2Trikafta 80 mg / 40 mg / 60 mg, 59.5 mg, GranulatA13 June 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
256Sachet(s)R07AX3203.99.0.A
156Sachet(s)R07AX3203.99.0.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Trikafta 100 mg / 50 mg / 75 mg authorised in Switzerland?

Yes. Trikafta 100 mg / 50 mg / 75 mg is authorised by Swissmedic under authorisation number 69212, data as of 01 September 2026. The authorisation is limited until 12 June 2029.

Which dispensing category does Trikafta 100 mg / 50 mg / 75 mg have?

Trikafta 100 mg / 50 mg / 75 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 Trikafta 100 mg / 50 mg / 75 mg?

The authorisation holder is Vertex Pharmaceuticals (CH) 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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