Wednesday, September 23, 2009

FDA Advisory Committee Hears Presentations and Public Comment on EXALGO Extended-Release Tablets

)--Sep 23, 2009 - Covidien, a leading global provider of healthcare products, today announced that it presented information to members of a U.S. Food and Drug Administration (FDA) Advisory Committee on the New Drug Application and proposed Risk Evaluation and Mitigation Strategy (REMS) program for EXALGOTM (hydromorphone HCl extended release) tablets, an opioid formulation.

The details can be read here.

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