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AVANIR Pharmaceuticals announces filing of Complete Response to FDA Approvable Letter for Zenvia AVANIR Pharmaceuticals, Inc. today announced the submission of its Full Response to the October 2006 Approvable Letter released by the U.S. AVANIR expects the FDA to classify the response as a Class 2 resubmission, which would result in an expected review period of 180 times and potential authorization of Zenvia in the 4th calendar quarter of 2010.