Tresiba Penfill

Tresiba Penfill is a medicine authorised by Swissmedic under authorisation number 62562. 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 12 March 2013 and the authorisation is valid without a time limit. ATC code A10AE06 places the medicine in the group Drugs used in diabetes.

  • Dispensing category B
  • Authorisation number 62562
  • ATC A10AE06
  • Biotechnological medicines
Authorisation data
Authorisation number62562
NameTresiba Penfill
Full nameTresiba Penfill, Injektionslösung
Authorisation holderNovo Nordisk Pharma AG
Medicinal product codeBiotechnological medicines
Dispensing categoryB · Prescription only
ATC codeA10AE06
First authorisation12 March 2013
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Tresiba Penfill, InjektionslösungB12 March 2013

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
15 x 3mlA10AE0607.06.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Tresiba Penfill authorised in Switzerland?

Yes. Tresiba Penfill is authorised by Swissmedic under authorisation number 62562, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Tresiba Penfill have?

Tresiba Penfill 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 Tresiba Penfill?

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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