Protonix

Cardinal Health 107, LLC🇺🇸 United States

FDA Page

Effective Date: Dec 16, 2022
Approval ID: 189b7b6a-9717-44eb-b87b-fd3e985b2268
Products: 1 registered
Version: 13

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use PROTONIX safely and effectively. See full prescribing information for PROTONIX. PROTONIX (pantoprazole sodium) delayed-release tablets, for oral usePROTONIX (pantoprazole sodium) for delayed-release oral suspensionInitial U.S. approval: 2000

Quick Stats

Total Products1

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.