Erelzi SensoReady 50 mg/1 ml

Erelzi SensoReady 50 mg/1 ml is a medicine authorised by Swissmedic under authorisation number 66176. The authorisation holder is Sandoz Pharmaceuticals AG. 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 18 May 2018 and the authorisation is valid without a time limit. ATC code L04AB01 places the medicine in the group Immunosuppressants.

  • Dispensing category B
  • Authorisation number 66176
  • ATC L04AB01
  • Biotechnological medicines
Authorisation data
Authorisation number66176
NameErelzi SensoReady 50 mg/1 ml
Full nameErelzi SensoReady 50 mg/1 ml, Injektionslösung im Fertigpen
Authorisation holderSandoz Pharmaceuticals AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codeL04AB01
First authorisation18 May 2018
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Erelzi SensoReady 50 mg/1 ml, Injektionslösung im FertigpenB18 May 2018

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Injektor(en), vorgefüllt/PenL04AB0107.15.0.B
22Injektor(en), vorgefüllt/PenL04AB0107.15.0.B
34Injektor(en), vorgefüllt/PenL04AB0107.15.0.B
412Injektor(en), vorgefüllt/PenL04AB0107.15.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Erelzi SensoReady 50 mg/1 ml authorised in Switzerland?

Yes. Erelzi SensoReady 50 mg/1 ml is authorised by Swissmedic under authorisation number 66176, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Erelzi SensoReady 50 mg/1 ml have?

Erelzi SensoReady 50 mg/1 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 Erelzi SensoReady 50 mg/1 ml?

The authorisation holder is Sandoz Pharmaceuticals 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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