Draxis radiopharmaceutical approved

AuntMinnie.com staff writers

Jan 12, 2006

Radiopharmaceutical developer Draxis Health has received FDA approval for its supplemental new drug application for sodium iodide I-131 oral capsules.

The capsules are intended to be used by physicians to perform radioactive iodide (RAI) uptake tests to evaluate thyroid function prior to treatment with stronger therapeutic doses of sodium iodide I-131, according to the Mississauga, Ontario-based firm. Diagnostic doses of sodium iodide I-131 may also be employed in localizing metastases associated with thyroid malignancies.

The capsules will be produced by the company's DraxImage subsidiary, and will be introduced in the U.S. market in the first half of 2006.

By AuntMinnie.com staff writers
January 13, 2006

Related Reading

Draxis iodine kit gets FDA approval, November 22, 2005

Draxis Health lowers expectations, November 21, 2005

Temporary shutdown hurts Draxis Health’s Q3, November 3, 2005

Draxis taps Brazier as COO, October 4, 2005

Draxis posts Q2 rise, August 11, 2005

Copyright © 2006 AuntMinnie.com

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