Actrapid HM

Actrapid HM is a medicine authorised by Swissmedic under authorisation number 44610. The authorisation holder is Novo Nordisk Pharma 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 22 August 1986 and the authorisation is valid without a time limit. ATC code A10AB01 places the medicine in the group Drugs used in diabetes.

  • Dispensing category B
  • Authorisation number 44610
  • ATC A10AB01
  • Biotechnological medicines
Authorisation data
Authorisation number44610
NameActrapid HM
Full nameActrapid HM, Injektionslösung
Authorisation holderNovo Nordisk Pharma AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codeA10AB01
First authorisation22 August 1986
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
2Actrapid HM, InjektionslösungB22 August 1986

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11 x 10 mlDurchstechflasche(n)A10AB0107.06.1.B
351 x 10 mlDurchstechflasche(n)A10AB0107.06.1.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Actrapid HM authorised in Switzerland?

Yes. Actrapid HM is authorised by Swissmedic under authorisation number 44610, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Actrapid HM have?

Actrapid HM 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 Actrapid HM?

The authorisation holder is Novo Nordisk Pharma 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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