Dexmedetomidin Fresenius i.v. 200ug/2ml

Dexmedetomidin Fresenius i.v. 200ug/2ml is a medicine authorised by Swissmedic under authorisation number 69275. The authorisation holder is Fresenius Kabi (Schweiz) 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 22 June 2023 and the authorisation is limited until 21 June 2028. ATC code N05CM18 places the medicine in the group Psycholeptics.

  • Dispensing category A
  • Authorisation number 69275
  • ATC N05CM18
  • Synthetic medicines
Authorisation data
Authorisation number69275
NameDexmedetomidin Fresenius i.v. 200ug/2ml
Full nameDexmedetomidin Fresenius i.v. 200ug/2ml, Konzentrat zur Herstellung einer Infusionslösung
Authorisation holderFresenius Kabi (Schweiz) AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeN05CM18
First authorisation22 June 2023
Authorisation validity21 June 2028
Strengths
No.NameDispensing categoryAuthorisation date
1Dexmedetomidin Fresenius i.v. 200ug/2ml, Konzentrat zur Herstellung einer InfusionslösungA22 June 2023
2Dexmedetomidin Fresenius i.v. 400ug/4ml, Konzentrat zur Herstellung einer InfusionslösungA22 June 2023
3Dexmedetomidin Fresenius i.v. 1000ug/10ml, Konzentrat zur Herstellung einer InfusionslösungA22 June 2023

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Durchstechflasche(n)N05CM1801.04.1.A
210Durchstechflasche(n)N05CM1801.04.1.A
310Durchstechflasche(n)N05CM1801.04.1.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Dexmedetomidin Fresenius i.v. 200ug/2ml authorised in Switzerland?

Yes. Dexmedetomidin Fresenius i.v. 200ug/2ml is authorised by Swissmedic under authorisation number 69275, data as of 01 September 2026. The authorisation is limited until 21 June 2028.

Which dispensing category does Dexmedetomidin Fresenius i.v. 200ug/2ml have?

Dexmedetomidin Fresenius i.v. 200ug/2ml 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 Dexmedetomidin Fresenius i.v. 200ug/2ml?

The authorisation holder is Fresenius Kabi (Schweiz) 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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