Beyfortus 50 mg/0.5 ml

Beyfortus 50 mg/0.5 ml is a medicine authorised by Swissmedic under authorisation number 69039. The authorisation holder is Sanofi-Aventis (Suisse) SA. 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 22 December 2023 and the authorisation is limited until 21 December 2028. ATC code J06BD08 places the medicine in the group Immune sera and immunoglobulins.

  • Dispensing category A
  • Authorisation number 69039
  • ATC J06BD08
  • Biotechnological medicines
Authorisation data
Authorisation number69039
NameBeyfortus 50 mg/0.5 ml
Full nameBeyfortus 50 mg/0.5 ml, solution injectable en seringue préremplie
Authorisation holderSanofi-Aventis (Suisse) SA
Medicinal product codeBiotechnological medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeJ06BD08
First authorisation22 December 2023
Authorisation validity21 December 2028
Strengths
No.NameDispensing categoryAuthorisation date
1Beyfortus 50 mg/0.5 ml, solution injectable en seringue préremplieA22 December 2023
2Beyfortus 100 mg/1 ml, solution injectable en seringue préremplieA22 December 2023

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Fertigspritze(n)J06BD0808.03.0.A
21Fertigspritze(n)J06BD0808.03.0.A
31Fertigspritze(n)J06BD0808.03.0.A
41Fertigspritze(n)J06BD0808.03.0.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Beyfortus 50 mg/0.5 ml authorised in Switzerland?

Yes. Beyfortus 50 mg/0.5 ml is authorised by Swissmedic under authorisation number 69039, data as of 01 September 2026. The authorisation is limited until 21 December 2028.

Which dispensing category does Beyfortus 50 mg/0.5 ml have?

Beyfortus 50 mg/0.5 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 Beyfortus 50 mg/0.5 ml?

The authorisation holder is Sanofi-Aventis (Suisse) SA. 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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