Northera

Lundbeck Pharmaceuticals LLC🇺🇸 United States

FDA Page

Effective Date: Jul 1, 2019
Approval ID: 2179f02c-48d7-48eb-8007-5ae43d8d16bc
Products: 3 registered
Version: 24

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use NORTHERA® safely and effectively. See full prescribing information for NORTHERA. NORTHERA® (droxidopa) capsules, for oral useInitial U.S. Approval: 2014

Quick Stats

Total Products3

Labelers2

Label Sections37

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.