Brukinsa 80 mg

Brukinsa 80 mg is a medicine authorised by Swissmedic under authorisation number 67998. 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 08 February 2022 and the authorisation is valid without a time limit. ATC code L01EL03 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 67998
  • ATC L01EL03
  • Synthetic medicines
Authorisation data
Authorisation number67998
NameBrukinsa 80 mg
Full nameBrukinsa 80 mg, Hartkapseln
Authorisation holderBeOne Medicines I GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01EL03
First authorisation08 February 2022
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Brukinsa 80 mg, HartkapselnA08 February 2022

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1120Kapsel(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 80 mg authorised in Switzerland?

Yes. Brukinsa 80 mg is authorised by Swissmedic under authorisation number 67998, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Brukinsa 80 mg have?

Brukinsa 80 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 80 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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