SUTAB

Azurity Pharmaceuticals, Inc.🇺🇸 United States

FDA Page

Effective Date: Jan 31, 2026
Approval ID: c020e973-dccf-4862-999e-17db6209a48a
Products: 1 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use SUTABsafely and effectively. See full prescribing information for SUTAB. SUTAB (sodium sulfate, magnesium sulfate, and potassium chloride) tablets, for oral use Initial U.S. Approval: 2020

Quick Stats

Total Products1

Labelers1

Label Sections18

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.