Albumin (Human)

Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.🇺🇸 United States

FDA Page

Effective Date: Aug 1, 2008
Approval ID: 90f0c351-3977-2b84-0a6a-e9cb091430ca
Products: 1 registered
Version: 5

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use ALBUMIN (HUMAN) 20% safely and effectively. See full prescribing information for ALBUMIN (HUMAN) 20%. ALBUMIN (HUMAN) 20% For intravenous use only 20% solution Initial U.S. Approval: 2006

Quick Stats

Total Products1

Labelers2

Label Sections16

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.