Makatussin Comp.

Makatussin Comp. is a medicine authorised by Swissmedic under authorisation number 39255. The authorisation holder is Gebro Pharma 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 29 June 1976 and the authorisation is valid without a time limit. ATC code R05DA20 places the medicine in the group Cough and cold preparations.

  • Dispensing category B
  • Authorisation number 39255
  • ATC R05DA20
  • Synthetic medicines
Authorisation data
Authorisation number39255
NameMakatussin Comp.
Full nameMakatussin Comp., Hustensirup
Authorisation holderGebro Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeR05DA20
First authorisation29 June 1976
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
3Makatussin Comp., HustensirupB26 May 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
3180mlR05DA2003.03.1.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Makatussin Comp. authorised in Switzerland?

Yes. Makatussin Comp. is authorised by Swissmedic under authorisation number 39255, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Makatussin Comp. have?

Makatussin Comp. 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 Makatussin Comp.?

The authorisation holder is Gebro Pharma 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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