YUTIQ

EyePoint Pharmaceuticals, Inc🇺🇸 United States

FDA Page

Effective Date: Dec 13, 2023
Approval ID: 43ba66d9-653d-48b9-9914-b0a50b68b79a
Products: 1 registered
Version: 11

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use YUTIQ safely and effectively. See full prescribing information for YUTIQ. YUTIQ (fluocinolone acetonide intravitreal implant) 0.18 mg, for intravitreal injection Initial U.S. Approval: 1963

Quick Stats

Total Products1

Labelers2

Label Sections14

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.