FDA
approval
· 2016-07-08
FDA Approved: LATUDA — Supplemental Application (Sumitomo Pharma America, Inc.)
Summary
FDA approved a supplemental application for LATUDA (lurasidone hydrochloride) submitted by Sumitomo Pharma America, Inc.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for LATUDA (LURASIDONE HYDROCHLORIDE)