Welireg 40 mg

Welireg 40 mg is a medicine authorised by Swissmedic under authorisation number 68531. The authorisation holder is MSD Merck Sharp & Dohme AG. 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 21 March 2024 and the authorisation is limited until 30 June 2030. ATC code L01XX74 places the medicine in the group Antineoplastic agents.

  • Dispensing category A
  • Authorisation number 68531
  • ATC L01XX74
  • Synthetic medicines
Authorisation data
Authorisation number68531
NameWelireg 40 mg
Full nameWelireg 40 mg, Filmtabletten
Authorisation holderMSD Merck Sharp & Dohme AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeL01XX74
First authorisation21 March 2024
Authorisation validity30 June 2030
Strengths
No.NameDispensing categoryAuthorisation date
1Welireg 40 mg, FilmtablettenA21 March 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
190Tablette(n)L01XX7407.16.4.A
290Tablette(n)L01XX7407.16.4.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Welireg 40 mg authorised in Switzerland?

Yes. Welireg 40 mg is authorised by Swissmedic under authorisation number 68531, data as of 01 September 2026. The authorisation is limited until 30 June 2030.

Which dispensing category does Welireg 40 mg have?

Welireg 40 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 Welireg 40 mg?

The authorisation holder is MSD Merck Sharp & Dohme 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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