divalproex sodium

First Nation Group, LLC🇺🇸 United States

FDA Page

Effective Date: Nov 19, 2025
Approval ID: a76f9909-28c9-4eb7-8ffd-ff6222fea079
Products: 1 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE CAPSULES safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE CAPSULES. DIVALPROEX SODIUM delayed-release capsules, for oral use Initial U.S. Approval: 1989

Quick Stats

Total Products1

Labelers2

Label Sections42

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.