RECOTHROM

Baxter Healthcare Corporation🇺🇸 United States

FDA Page

Effective Date: Jun 9, 2025
Approval ID: 54885644-e51e-4263-aadb-366abaeb56a3
Products: 3 registered
Version: 12

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use RECOTHROM safely and effectively. See full prescribing information for RECOTHROM.RECOTHROM Thrombin topical (Recombinant)Lyophilized Powder for Solution – For Topical Use OnlyInitial U.S. Approval: 2008

Quick Stats

Total Products3

Labelers2

Label Sections32

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.