Rapiscan 400 µg/ 5 ml

Rapiscan 400 µg/ 5 ml is a medicine authorised by Swissmedic under authorisation number 66137. The authorisation holder is GE Healthcare 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 28 July 2017 and the authorisation is valid without a time limit. ATC code C01EB21 places the medicine in the group Cardiac therapy.

  • Dispensing category A
  • Authorisation number 66137
  • ATC C01EB21
  • Synthetic medicines
Authorisation data
Authorisation number66137
NameRapiscan 400 µg/ 5 ml
Full nameRapiscan 400 µg/ 5 ml, Injektionslösung
Authorisation holderGE Healthcare AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeC01EB21
First authorisation28 July 2017
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Rapiscan 400 µg/ 5 ml, InjektionslösungA28 July 2017

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
11Durchstechflasche(n)C01EB2114.03.0.A

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Other medicines from this authorisation holder

Frequently asked questions

Is Rapiscan 400 µg/ 5 ml authorised in Switzerland?

Yes. Rapiscan 400 µg/ 5 ml is authorised by Swissmedic under authorisation number 66137, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Rapiscan 400 µg/ 5 ml have?

Rapiscan 400 µg/ 5 ml 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 Rapiscan 400 µg/ 5 ml?

The authorisation holder is GE Healthcare 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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