Uniferon® approved in UK (replaces Leodex®)

May 18, 2006

Uniferon® has been approved by the Veterinary Medicines Directorate in the United Kingdom (UK) and replaces Leodex®. Uniferon® is Pharmacosmos' veterinary Iron Dextran compound for injection and the worldwide leading injectable Iron Dextran solution for prevention of iron deficiency anemia in piglets.

Leodex® in the UK

Since 1992, Pharmacosmos has supplied the active pharmaceutical ingredient (API) in Leodex® veterinary Iron Dextran solution for injection. Leodex® has been marketed by Leo Laboratories Ltd., a UK subsidiary of Danish-based pharmaceutical company Leo Pharma A/S.

As a natural extension of Pharmacosmos' commitment the UK customers, Pharmacosmos is pleased to announce that the company agreed to acquire Leo Laboratories Ltd.'s marketing authorization of Leodex® earlier in 2006.

Uniferon® replaces Leodex®

As an important part of the procedure of acquiring the marketing authorization of Leodex®, Pharmacosmos has decided to let Uniferon® replace Leodex® as product name. This will allow UK customers to benefit from the strong awareness of the documented positive effects of Uniferon®. Today, Uniferon® has been approved by the UK Veterinary Medicines Directorate.

About Uniferon®

Injection of Uniferon® provides high 200 mg iron per ml for treatment and is an efficient method to prevent iron deficiency anemia. Ensuring healthy and vigorous growth in piglets, Uniferon® has been approved in all major countries including the United States (US).

Please read more information about Uniferon®.

About Pharmacosmos A/S

Pharmacosmos A/S is a Danish pharmaceutical company that manufactures and markets injectable iron pharmaceuticals for iron repletion in humans and Dextran used in various clinical and technical compounds including solutions for infusion.

Pharmacosmos is one of the leading companies within its area of business and markets its products in more than 50 countries worldwide. The manufacturing is controlled and approved the Danish Medicines Agency and the US Food & Drug Administration.

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