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A Bioavailability Crossover Study of Two Formulations of Lamotrigine Extended Release Tablets in Healthy Subjects

Food and Drug Administration (FDA) · 2016
ClinicalTrials.gov · Datasets · License: Public Domain · 2016
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The objective of this study is to determine bioequivalence between two different formulations of lamotrigine extended release tablets (one reference product and one generic product) in a healthy adult population, following a single oral dose under fed conditions.
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