FDA Approved: LATUDA — Supplemental Application (Sumitomo Pharma America, Inc.)

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Summary

The FDA approved a supplemental application for Latuda (lurasidone hydrochloride) from Sumitomo Pharma America, Inc. to update the product labeling.

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Diseases / indications

• Bipolar Disorder Depressive Episodes
• Schizophrenia

Drugs mentioned

• Latuda (lurasidone)

Snippet

SUPPL AP for LATUDA (LURASIDONE HYDROCHLORIDE)