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You are here: Industry Insights > FDA acceptance

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Sunovion Announces FDA Acceptance for Review of sNDA for Latuda for Bipolar Depression americanpharmaceuticalreview
July 04, 2017
Sunovion Pharmaceuticals announced the U.S. Food and Drug Administration (FDA) has accepted for review the supplemental New Drug Application (sNDA) for the expanded use of Latuda (lurasidone HCI) in children...

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