Flucoderm 50 mg

Flucoderm 50 mg is a medicine authorised by Swissmedic under authorisation number 58061. The authorisation holder is Dermapharm 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 27 August 2007 and the authorisation is valid without a time limit. ATC code J02AC01 places the medicine in the group Antimycotics for systemic use.

  • Dispensing category B
  • Authorisation number 58061
  • ATC J02AC01
  • Synthetic medicines
Authorisation data
Authorisation number58061
NameFlucoderm 50 mg
Full nameFlucoderm 50 mg, Kapseln
Authorisation holderDermapharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeJ02AC01
First authorisation27 August 2007
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Flucoderm 50 mg, KapselnB27 August 2007
2Flucoderm 100 mg, KapselnB27 August 2007
3Flucoderm 150 mg, KapselnB27 August 2007
4Flucoderm 200 mg, KapselnB27 August 2007

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
27Kapsel(n)J02AC0108.06.0.B
428Kapsel(n)J02AC0108.06.0.B
64Kapsel(n)J02AC0108.06.0.B
87Kapsel(n)J02AC0108.06.0.B
1014Kapsel(n)J02AC0108.06.0.B
121Kapsel(n)J02AC0108.06.0.B
144Kapsel(n)J02AC0108.06.0.B
162Kapsel(n)J02AC0108.06.0.B
187Kapsel(n)J02AC0108.06.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Flucoderm 50 mg authorised in Switzerland?

Yes. Flucoderm 50 mg is authorised by Swissmedic under authorisation number 58061, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Flucoderm 50 mg have?

Flucoderm 50 mg 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 Flucoderm 50 mg?

The authorisation holder is Dermapharm 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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