KEBILIDI

🇺🇸 United States

FDA Page

Effective Date: Jun 11, 2026
Approval ID: 9d6a6401-c6b5-4f29-af11-67707d249482
Products: 0 registered
Version: 4

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use KEBILIDI safely and effectively. See full prescribing information for KEBILIDI. KEBILIDI (eladocagene exuparvovec-tneq) suspension, for intraputaminal infusion Initial U.S. Approval: 2024

Quick Stats

Total Products0

Labelers0

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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.