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See Latest ArticlesFDA grants marketing approval for Lundbeck's Sabril (vigabatrin)
Lundbeck, 08/24/09
H. Lundbeck A/S announced that the US Food and Drug Administration (FDA) has granted two New Drug Application (NDA) approvals for Sabril Tablets and Oral Solution. Lundbeck Inc. plans to launch Sabril in the US during the third quarter of 2009, with an extensive Risk Evaluation and Mitigation Strategy (REMS) program as required by the FDA and created in collaboration with the agency.
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Today in Drug Trials...keeping you current
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A 25-week, open-label trial investigating rivastigmine transdermal patches with concomitant memantine in mild-to-moderate Alzheimers disease: a post hoc analysis
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