XELPROS

Sun Pharmaceutical Industries, Inc.🇺🇸 United States

FDA Page

Effective Date: Dec 18, 2025
Approval ID: 34ad5cf6-4df0-4104-bddd-4c7631133ded
Products: 1 registered
Version: 9

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use XELPROS safely and effectively. See full prescribing information for XELPROS. XELPROS(latanoprost ophthalmic emulsion) 0.005%, for topical ophthalmic useInitial U.S. Approval: 1996

Quick Stats

Total Products1

Labelers2

Label Sections21

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.