FDA Approved: DEPAKOTE ER — Supplemental Application (AbbVie Inc.)

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Summary

The FDA approved a supplemental application for Depakote ER (divalproex sodium) filed by AbbVie Inc., resulting in a regulatory update to the product label.

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Diseases / indications

• Bipolar Disorder
• Epilepsy
• Migraine

Drugs mentioned

• DEPAKOTE ER (DIVALPROEX SODIUM)

Snippet

SUPPL AP for DEPAKOTE ER (DIVALPROEX SODIUM)