Seffalair Spiromax 55/14 mcg

Seffalair Spiromax 55/14 mcg is a medicine authorised by Swissmedic under authorisation number 67891. The authorisation holder is Teva 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 12 April 2021 and the authorisation is valid without a time limit. ATC code R03AK06 places the medicine in the group Drugs for obstructive airway diseases.

  • Dispensing category B
  • Authorisation number 67891
  • ATC R03AK06
  • Synthetic medicines
Authorisation data
Authorisation number67891
NameSeffalair Spiromax 55/14 mcg
Full nameSeffalair Spiromax 55/14 mcg, Multidosenpulverinhalator
Authorisation holderTeva Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeR03AK06
First authorisation12 April 2021
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Seffalair Spiromax 55/14 mcg, MultidosenpulverinhalatorB12 April 2021
2Seffalair Spiromax 113/14 mcg, MultidosenpulverinhalatorB12 April 2021
3Seffalair Spiromax 232/14 mcg, MultidosenpulverinhalatorB12 April 2021

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
160StückR03AK0603.04.3.B
260StückR03AK0603.04.3.B
360StückR03AK0603.04.3.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Seffalair Spiromax 55/14 mcg authorised in Switzerland?

Yes. Seffalair Spiromax 55/14 mcg is authorised by Swissmedic under authorisation number 67891, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Seffalair Spiromax 55/14 mcg have?

Seffalair Spiromax 55/14 mcg 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 Seffalair Spiromax 55/14 mcg?

The authorisation holder is Teva 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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