Duodart

Duodart is a medicine authorised by Swissmedic under authorisation number 60095. The authorisation holder is GlaxoSmithKline 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 17 March 2010 and the authorisation is valid without a time limit. ATC code G04CA52 places the medicine in the group Urologicals.

  • Dispensing category B
  • Authorisation number 60095
  • ATC G04CA52
  • Synthetic medicines
Authorisation data
Authorisation number60095
NameDuodart
Full nameDuodart, Hartkapseln
Authorisation holderGlaxoSmithKline AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeG04CA52
First authorisation17 March 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Duodart, HartkapselnB17 March 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
230Kapsel(n)G04CA5205.99.0.B
390Kapsel(n)G04CA5205.99.0.B
77Kapsel(n)G04CA5205.99.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Duodart authorised in Switzerland?

Yes. Duodart is authorised by Swissmedic under authorisation number 60095, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Duodart have?

Duodart 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 Duodart?

The authorisation holder is GlaxoSmithKline 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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