Dupixent 300 mg/2 ml

Dupixent 300 mg/2 ml is a medicine authorised by Swissmedic under authorisation number 66649. The authorisation holder is Sanofi-Aventis (Suisse) SA. The medicinal product code is Biotechnological medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 05 April 2019 and the authorisation is valid without a time limit. ATC code D11AH05 places the medicine in the group Other dermatological preparations.

  • Dispensing category B
  • Authorisation number 66649
  • ATC D11AH05
  • Biotechnological medicines
Authorisation data
Authorisation number66649
NameDupixent 300 mg/2 ml
Full nameDupixent 300 mg/2 ml, solution injectable en seringue préremplie avec système de sécurité
Authorisation holderSanofi-Aventis (Suisse) SA
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codeD11AH05
First authorisation05 April 2019
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Dupixent 300 mg/2 ml, solution injectable en seringue préremplie avec système de sécuritéB05 April 2019
2Dupixent 200 mg/1.14 ml, solution injectable en seringue préremplie avec système de sécuritéB19 November 2020

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
12Fertigspritze(n)D11AH0507.15.0.B
22Fertigspritze(n)D11AH0507.15.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Dupixent 300 mg/2 ml authorised in Switzerland?

Yes. Dupixent 300 mg/2 ml is authorised by Swissmedic under authorisation number 66649, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Dupixent 300 mg/2 ml have?

Dupixent 300 mg/2 ml is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.

Who is the authorisation holder of Dupixent 300 mg/2 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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