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FDA expands label for GlaxoSmithKline's antiepileptic Lamictal XR

This article was originally published in Scrip

Executive Summary

The US FDA has expanded the label of GlaxoSmithKline's once-daily Lamictal XR (lamotrigine) extended release tablets to include add-on treatment of epilepsy in patients aged 13 years and older with primary generalized tonic-clonic seizures.


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