Olopatadine

Akorn🇺🇸 United States

FDA Page

Effective Date: Feb 3, 2022
Approval ID: 7de7f9ea-53e3-4f03-b60d-31a2817b5f49
Products: 1 registered
Version: 3

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use Olopatadine Hydrochloride Ophthalmic Solution USP, 0.2% safely and effectively. See full prescribing information for Olopatadine Hydrochloride Ophthalmic Solution USP, 0.2%.Olopatadine Hydrochloride Ophthalmic Solution USP, 0.2%Initial U.S. Approval: 1996

Quick Stats

Total Products1

Labelers2

Label Sections29

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.