Nexiclon XR

Athena Bioscience, LLC🇺🇸 United States

FDA Page

Effective Date: Apr 15, 2026
Approval ID: dad35a6f-d57e-f302-e053-2995a90a9efb
Products: 1 registered
Version: 2

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

NEXICLON™ XR (clonidine) Extended-Release Tablets These highlights do not include all the information needed to use NEXICLON™ XR (clonidine) Extended-Release Tablets safely and effectively. See full prescribing information for NEXICLON™ XR (clonidine) Extended-Release Tablets. NEXICLON™ XR (clonidine) Extended-Release Tablets Initial U.S. Approval: 1974

Quick Stats

Total Products1

Labelers2

Label Sections17

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.