Cardiolite

🇺🇸 United States

FDA Page

Effective Date: Sep 10, 2026
Approval ID: 773b6729-2a74-49e7-9215-ca70da3b854c
Products: 0 registered
Version: 2

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use CARDIOLITE safely and effectively. See full prescribing information for CARDIOLITE. CARDIOLITE®, Kit for the Preparation of Technetium Tc99m Sestamibi for Injection Initial U.S. Approval: December, 1990

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.