Zolpidem tartrate

Par Pharmaceutical, Inc.🇺🇸 United States

FDA Page

Effective Date: Oct 1, 2019
Approval ID: b8b57980-d3ef-49aa-a30f-3090d2ebb305
Products: 2 registered
Version: 33

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use ZOLPIDEM TARTRATE SUBLINGUAL TABLETS safely and effectively. See full prescribing information for ZOLPIDEM TARTRATE SUBLINGUAL TABLETS . ZOLPIDEM TARTRATE sublingual tablets, for oral use, CIV Initial U.S. Approval: 1992

Quick Stats

Total Products2

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.