Hulio 40 mg/0.8 ml

Hulio 40 mg/0.8 ml is a medicine authorised by Swissmedic under authorisation number 67612. The authorisation holder is Medius 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 13 May 2020 and the authorisation is valid without a time limit. The export lists no ATC code for this medicine.

  • Dispensing category B
  • Authorisation number 67612
  • Biotechnological medicines
Authorisation data
Authorisation number67612
NameHulio 40 mg/0.8 ml
Full nameHulio 40 mg/0.8 ml, Injektionslösung in einer Durchstechflasche
Authorisation holderMedius AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codenot stated
First authorisation13 May 2020
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Hulio 40 mg/0.8 ml, Injektionslösung in einer DurchstechflascheB13 May 2020

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
The Swissmedic export lists no pack sizes for this medicine.

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Other medicines from this authorisation holder

Frequently asked questions

Is Hulio 40 mg/0.8 ml authorised in Switzerland?

Yes. Hulio 40 mg/0.8 ml is authorised by Swissmedic under authorisation number 67612, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Hulio 40 mg/0.8 ml have?

Hulio 40 mg/0.8 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 Hulio 40 mg/0.8 ml?

The authorisation holder is Medius 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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