LURASIDONE HYDROCHLORIDE

Aurobindo Pharma Limited🇺🇸 United States

FDA Page

Effective Date: Mar 29, 2023
Approval ID: b3e9cc86-0c5c-444f-ab57-f4d1a6865035
Products: 5 registered
Version: 2

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use LURASIDONE HYDROCHLORIDE TABLETS safely and effectively. See full prescribing information for LURASIDONE HYDROCHLORIDE TABLETS. LURASIDONE HYDROCHLORIDE tablets, for oral use Initial U.S. Approval: 2010

Quick Stats

Total Products5

Labelers2

Label Sections23

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.