memantine hydrochloride

Sun Pharmaceutical Industries, Inc.🇺🇸 United States

FDA Page

Effective Date: Dec 27, 2019
Approval ID: e16a8aa8-f5fd-4db8-abb2-d54e742bb95f
Products: 4 registered
Version: 6

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use MEMANTINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES safely and effectively. See full prescribing information for MEMANTINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES. MEMANTINE HYDROCHLORIDE extended-release capsules, for oral use Initial U.S. Approval: 2003

Quick Stats

Total Products4

Labelers2

Label Sections20

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.