Empirical findings have demonstrated that the application of an N-Methyl-D-aspartate (NMDA) receptor antagonist effectively prevents the formation of morphine-induced location preference. Eugenol, the primary constituent found in the extract of S. aromaticum (SA), exhibits notable efficacy in traversing the blood-brain barrier and possesses inhibitory properties against the metabotropic NMDA receptor. This study aimed to evaluate the actions of the hydro-alcoholic extract of S. aromaticum on the acquisition and expression of morphine-induced conditioned place preference (CPP) in mice, followed by in silico studies. The conditioned place preference (CPP) test was used for investigating addictive-seeking behavior. Morphine (5 mg/kg) was used to produce CPP, and saline was used as a control. Morphine significantly increased the preference scores on the drug-paired side (p<0.001), whereas both doses of S. aromaticum extract (200 and 400 mg/kg) did not reveal any liking compared to the control group. Higher doses of S. aromaticum extract (400 mg/kg) reduced the acquisition of MOR-induced CPP (p<0.001) but had no significant effect on the expression of morphine CPP. Molecular docking analysis showed that the binding affinities of eugenol to NMDA receptor are -5.1 kcal/mol, comparable to the reference NMDA antagonist memantine which has -5.6 kcal/mol binding affinity to NMDA receptor. Eugenol formed hydrophobic bonds with NMDA receptors at VAL644, PHE554, TRP563 and TYR647 residues, comparable to the binding affinity of NMDA antagonist memantine. ADMET analysis showed that eugenol has high intestinal absorption and good bioavailability (>90%) and can cross the BBB easily (logBB> 0.3). On the basis of our in vivo trials and in silico report, we settled that the acquisition effect of S. aromaticum might be due to the antioxidant and antagonistic properties of eugenol to NMDA receptor. It would be reasonable to conduct mechanistic research in the forthcoming days to elucidate the underlying mechanisms utilizing various methodologies. Dhaka Univ. J. Pharm. Sci. 23(1): 77-92, 2024 (June)