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Meda files Dymista MAA in Europe

Meda has registered a marketing authorization application (MAA) of its Dymista in Europe.

The MAA includes the efficacy and safety data of several studies involving over 4,000 patients, and also includes a long-term safety study with more than 600 patients.

Dymista is formulated with azelastine hydrochloride and fluticasone propionate and is used as a nasal spray formulation to treat moderate to severe allergic rhinitis and rhinoconjuctivitis.