Ruxience 100 mg/10 ml

Ruxience 100 mg/10 ml is a medicine authorised by Swissmedic under authorisation number 69701. The authorisation holder is Pfizer AG. The medicinal product code is Biotechnological 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 19 August 2024 and the authorisation is limited until 18 August 2029. ATC code L01FA01 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 69701
  • ATC L01FA01
  • Biotechnological medicines
Authorisation data
Authorisation number69701
NameRuxience 100 mg/10 ml
Full nameRuxience 100 mg/10 ml, Konzentrat zur Herstellung einer Infusionslösung
Authorisation holderPfizer AG
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01FA01
First authorisation19 August 2024
Authorisation validity18 August 2029
Strengths
No.NameDispensing categoryAuthorisation date
1Ruxience 100 mg/10 ml, Konzentrat zur Herstellung einer InfusionslösungA19 August 2024
2Ruxience 500 mg/50 ml, Konzentrat zur Herstellung einer InfusionslösungA19 August 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Durchstechflasche(n)L01FA0107.16.1.A
32 x 1Durchstechflasche(n)L01FA0107.16.1.A
21Durchstechflasche(n)L01FA0107.16.1.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ruxience 100 mg/10 ml authorised in Switzerland?

Yes. Ruxience 100 mg/10 ml is authorised by Swissmedic under authorisation number 69701, data as of 01 September 2026. The authorisation is limited until 18 August 2029.

Which dispensing category does Ruxience 100 mg/10 ml have?

Ruxience 100 mg/10 ml 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 Ruxience 100 mg/10 ml?

The authorisation holder is Pfizer 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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