Verkazia

Harrow Eye, LLC🇺🇸 United States

FDA Page

Effective Date: Jun 3, 2026
Approval ID: 48651d30-9e6e-74b0-e063-6294a90a8337
Products: 1 registered
Version: 5

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use VERKAZIA safely and effectively. See full prescribing information for VERKAZIA. Verkazia® (cyclosporine ophthalmic emulsion) 0.1%, for topical ophthalmic use Initial U.S. Approval: 1983

Quick Stats

Total Products1

Labelers1

Label Sections15

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.