Dorzolamide Hydrochloride

Sagent Pharmaceuticals🇺🇸 United States

FDA Page

Effective Date: Jan 9, 2026
Approval ID: 0246463c-6c24-4611-8e22-2d5254ace66a
Products: 1 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use DORZOLAMIDE HYDROCHLORIDE OPHTHALMIC SOLUTION safely and effectively. See full prescribing information for DORZOLAMIDE HYDROCHLORIDE OPHTHALMIC SOLUTION. DORZOLAMIDE HYDROCHLORIDE ophthalmic solution 2%, for topical ophthalmic use Initial U.S. Approval: 1994

Quick Stats

Total Products1

Labelers1

Label Sections17

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.