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EMA Product

Seffalair Spiromax

Product approved by European Medicines Agency (EU)

Basic Information

Seffalair Spiromax

Regulatory Information

EMEA/H/C/004881

Authorised

March 26, 2021

2

August 23, 2021

Company Information

the netherlands

Swensweg 5 2031GA Haarlem

Teva Pharma B.V.

Active Substances Detail

fluticasone propionatesalmeterol xinafoate

Detailed Information

Therapeutic Indication

### Therapeutic indication Seffalair Spiromax is indicated in the regular treatment of asthma in adults and adolescents aged 12 years and older not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled short-acting ?? agonists.

Overview Summary

Seffalair Spiromax is a medicine used for the regular treatment of asthma in adults and adolescents above 12 years of age. It is used in patients whose disease is not adequately controlled despite treatment with a combination of a short-acting beta-2 agonist and inhaled corticosteroid. It contains the active substances salmeterol and fluticasone.

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