Amiodar

Amiodar is a medicine authorised by Swissmedic under authorisation number 55721. The authorisation holder is Sandoz Pharmaceuticals 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 19 May 2004 and the authorisation is valid without a time limit. ATC code C01BD01 places the medicine in the group Cardiac therapy.

  • Dispensing category B
  • Authorisation number 55721
  • ATC C01BD01
  • Synthetic medicines
Authorisation data
Authorisation number55721
NameAmiodar
Full nameAmiodar, Tabletten
Authorisation holderSandoz Pharmaceuticals AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC01BD01
First authorisation19 May 2004
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
2Amiodar, TablettenB19 May 2004

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
220Tablette(n)C01BD0102.02.0.B
460Tablette(n)C01BD0102.02.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Amiodar authorised in Switzerland?

Yes. Amiodar is authorised by Swissmedic under authorisation number 55721, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Amiodar have?

Amiodar 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 Amiodar?

The authorisation holder is Sandoz Pharmaceuticals 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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