EC-NAPROXEN

Bryant Ranch Prepack🇺🇸 United States

FDA Page

Effective Date: Dec 8, 2023
Approval ID: d6443cba-5593-4bd1-8137-af12b4103790
Products: 1 registered
Version: 103

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use NAPROXEN Tablets, EC-NAPROXEN and NAPROXEN SODIUM safely and effectively. See full prescribing information for NAPROXEN, EC-NAPROXEN and NAPROXEN SODIUM. NAPROXEN (naproxen) tablets, EC-NAPROXEN (naproxen delayed-release tablets), NAPROXEN SODIUM (naproxen sodium tablets), for oral use Initial U.S. Approval: 1976

Quick Stats

Total Products1

Labelers2

Label Sections19

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.