- Regulatory authorities in Ireland and Czech Republic grant marketing authorizations for AirFluSal® Forspiro®
- Approval for 50-250 and 50-500µg dosage forms
- AirFluSal Forspiro already launched in four European countries and South Korea
Holzkirchen, November 19, 2014 – Sandoz announces today that the pharmaceutical regulatory authorities in Ireland and the Czech Republic have granted marketing authorizations for AirFluSal® Forspiro®, an innovative new inhaler for patients with asthma and/or chronic obstructive pulmonary disease (COPD).
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