ACULAR LS

Allergan, Inc.🇺🇸 United States

FDA Page

Effective Date: Mar 1, 2021
Approval ID: 4fad0873-f79c-4f07-9fac-5060be6b38fe
Products: 1 registered
Version: 15

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use ACULAR LS safely and effectively. See full prescribing information for ACULAR LS. ACULAR LS (ketorolac tromethamine ophthalmic solution) 0.4% , for topical ophthalmic use Initial U.S. Approval: 1991

Quick Stats

Total Products1

Labelers2

Label Sections13

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.