venlafaxine hydrochloride, extended release

Edenbridge Pharmaceuticals LLC.🇺🇸 United States

FDA Page

Effective Date: Jan 4, 2024
Approval ID: 38431a76-6185-4c17-994f-8278b6cd7510
Products: 2 registered
Version: 3

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use Venlafaxine Hydrochloride Extended-Release Tablets safely and effectively. See full prescribing information for Venlafaxine Hydrochloride Extended-Release Tablets. Venlafaxine Hydrochloride Extended-Release Tablets, for oral use. Initial U.S. Approval: 1993

Quick Stats

Total Products2

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.