GW gains first approval for Seretide MDI
Glaxo Wellcome has received its first approval, from the UK'sMedicines Control Agency, to market Seretide (fluticasone propionate and salmeterol xinafoate) in a metered dose inhaler. The product was launched last year in the dry powder Diskus inhaler formulation. The company says that while "Seretide has already enjoyed notable commercial success....the MDI, used by 70% of patients worldwide, remains the mainstay of asthma treatment." The UK will now act as reference member state for European Union approval.
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