memantine

Chartwell RX, LLC🇺🇸 United States

FDA Page

Effective Date: Feb 2, 2023
Approval ID: 6906b0b4-1944-40f0-844a-e0db72ba4675
Products: 2 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 MEMANTINE HYDROCHLORIDE TABLETS, USP safely and effectively. See full prescribing information for MEMANTINE HYDROCHLORIDE TABLETS, USP. MEMANTINE HYDROCHLORIDE TABLETS, USP for oral use Initial U.S. Approval: 2003

Quick Stats

Total Products2

Labelers2

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.