Brukinsa 160 mg

Brukinsa 160 mg is a medicine authorised by Swissmedic under authorisation number 69945. The authorisation holder is BeOne Medicines I 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 27 October 2025 and the authorisation is limited until 26 October 2030. ATC code L01EL03 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 69945
  • ATC L01EL03
  • Synthetic medicines
Authorisation data
Authorisation number69945
NameBrukinsa 160 mg
Full nameBrukinsa 160 mg, Filmtabletten
Authorisation holderBeOne Medicines I GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01EL03
First authorisation27 October 2025
Authorisation validity26 October 2030
Strengths
No.NameDispensing categoryAuthorisation date
1Brukinsa 160 mg, FilmtablettenA27 October 2025

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
160Tablette(n)L01EL0307.16.1.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Brukinsa 160 mg authorised in Switzerland?

Yes. Brukinsa 160 mg is authorised by Swissmedic under authorisation number 69945, data as of 01 September 2026. The authorisation is limited until 26 October 2030.

Which dispensing category does Brukinsa 160 mg have?

Brukinsa 160 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 Brukinsa 160 mg?

The authorisation holder is BeOne Medicines I 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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