Resonium-A

Resonium-A is a medicine authorised by Swissmedic under authorisation number 33379. The authorisation holder is Sanofi-Aventis (Suisse) SA. 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 22 April 1968 and the authorisation is valid without a time limit. ATC code V03AE01 places the medicine in the group All other therapeutic products.

  • Dispensing category B
  • Authorisation number 33379
  • ATC V03AE01
  • Synthetic medicines
Authorisation data
Authorisation number33379
NameResonium-A
Full nameResonium-A, poudre
Authorisation holderSanofi-Aventis (Suisse) SA
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeV03AE01
First authorisation22 April 1968
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Resonium-A, poudreB22 April 1968

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
13450gV03AE0116.00.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Resonium-A authorised in Switzerland?

Yes. Resonium-A is authorised by Swissmedic under authorisation number 33379, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Resonium-A have?

Resonium-A 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 Resonium-A?

The authorisation holder is Sanofi-Aventis (Suisse) SA. 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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