Nowadays, pharmaceutical cocrystals are an alternative approach to the synthesis of new solids without altering active pharmaceutical ingredients of the drug. In this study, lamotrigine (LTG) theophylline (THP) cocrystal monohydrate (1:1:1) and LTG glutarimide (GLU) cocrystal (1:1) were synthesized and characterized by single-crystal X-ray diffraction, powder X-ray diffraction, and Fourier transform infrared analysis. The Hirshfeld surface and 2D fingerprint of the LTG molecule in LTG-THP-H2O and LTG-GLU indicated that the main intermolecular forces between two LTG coaystals molecules are H center dot center dot center dot N/N center dot center dot center dot H and H center dot center dot center dot O. Dissolution results and stability studies demonstrated that the properties of LTG were enhanced by coaystal formation. Contrary to LTG-GLU, LTG-THP-H2O posed slower dissolution rate and higher stability capability, which can be ascribed to the hydrated structure in LTG-THP-H2O and the aminopyridine dimer structure in LTG-GLU. Hence, it is necessary to select the conformers purposefully as to improve the corresponding performance of LTG. (C) 2020 Elsevier B.V. All rights reserved.