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Acrux Says Europe Marketing Authorization for Recuvyra Granted

Oct. 13 (Bloomberg) -- Acrux Ltd. said the European Medicines Agency has granted the marketing authorization for commercial use of Recuvyra 50 mg/mL transdermal solution for dogs, according to a regulatory filing.

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To contact the editor responsible for this story: Victoria Batchelor at vbatchelor@bloomberg.net

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