Sugammadex Fresenius i.v. 200 mg/2 ml

Sugammadex Fresenius i.v. 200 mg/2 ml is a medicine authorised by Swissmedic under authorisation number 69703. The authorisation holder is Fresenius Kabi (Schweiz) AG. The medicinal product code is Synthetic 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 15 November 2024 and the authorisation is limited until 14 November 2029. ATC code V03AB35 places the medicine in the group All other therapeutic products.

  • Dispensing category B
  • Authorisation number 69703
  • ATC V03AB35
  • Synthetic medicines
Authorisation data
Authorisation number69703
NameSugammadex Fresenius i.v. 200 mg/2 ml
Full nameSugammadex Fresenius i.v. 200 mg/2 ml, Injektionslösung
Authorisation holderFresenius Kabi (Schweiz) AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeV03AB35
First authorisation15 November 2024
Authorisation validity14 November 2029
Strengths
No.NameDispensing categoryAuthorisation date
2Sugammadex Fresenius i.v. 200 mg/2 ml, InjektionslösungB15 November 2024
3Sugammadex Fresenius i.v. 500 mg/5 ml, InjektionslösungB15 November 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Durchstechflasche(n)V03AB3515.01.0.B
210Durchstechflasche(n)V03AB3515.01.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Sugammadex Fresenius i.v. 200 mg/2 ml authorised in Switzerland?

Yes. Sugammadex Fresenius i.v. 200 mg/2 ml is authorised by Swissmedic under authorisation number 69703, data as of 01 September 2026. The authorisation is limited until 14 November 2029.

Which dispensing category does Sugammadex Fresenius i.v. 200 mg/2 ml have?

Sugammadex Fresenius i.v. 200 mg/2 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 Sugammadex Fresenius i.v. 200 mg/2 ml?

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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