Duloxetine hydrochloride

Proficient Rx LP🇺🇸 United States

FDA Page

Effective Date: Jan 1, 2021
Approval ID: 510ceafd-8254-428c-b2ff-a167f283cda7
Products: 1 registered
Version: 4

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use duloxetine delayed-release capsules, USP safely and effectively. See full prescribing information for duloxetine delayed-release capsules, USP.DULOXETINE delayed-release capsules USP, for oral use.Initial U.S. Approval: 2004

Quick Stats

Total Products1

Labelers2

Label Sections21

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.