Zohydro

Zogenix, Inc.🇺🇸 United States

FDA Page

Effective Date: Feb 25, 2015
Approval ID: 6ccfbd98-7750-4955-a654-ec104fb666f9
Products: 6 registered
Version: 20

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use ZOHYDRO ER safely and effectively. See full prescribing information for ZOHYDRO ER. ZOHYDRO ER (hydrocodone bitartrate) extended‑release capsules, for oral use, CII Initial U.S. Approval: 1943

Quick Stats

Total Products6

Labelers2

Label Sections25

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.