FESILTY

🇺🇸 United States

FDA Page

Effective Date: Aug 20, 2026
Approval ID: 1b470116-54bc-4ef8-ae46-2fba06c3368b
Products: 0 registered
Version: 5

Regulatory Information

Labeling Type

PLASMA DERIVATIVE

Status

Approved

Full Title

These highlights do not include all the information needed to use FESILTY safely and effectively. See full prescribing information for FESILTY. FESILTY (fibrinogen, human - chmt), lyophilized powder for reconstitution, for intravenous useInitial U.S. Approval: 2025

Quick Stats

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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.