A liquid chromatographic method is described for the simultaneous determination of cefalexin and trimethoprim in dog plasma. A simple protein precipitation procedure was adopted for the sample preparation with satisfactory extraction recoveries for both analytes. Chromatographic separation of the analytes was achieved on a C 18 column using a mixture of 2mol/l formate buffer (pH 3.5), methanol and acetonitrile (22:7:7, v/v/v) containing a 0.002mol/l sodium dodecyl sulfate as mobile phase and detection was performed at 240nm. The linearity was obtained over the concentration ranges of 1.0–100.0μg/ml for cefalexin and 0.5–50.0μg/ml for trimethoprim. For each level of QC samples including the lower limit of quantification, both inter- and intra-day precisions (R.S.D.) were ≤14.0% for cefalexin and ≤11.4% for trimethoprim, and accuracy (RE) was −1.4% for cefalexin and −3.0% for trimethoprim. The present LC method was successfully applied to the pharmacokinetic studies of coformulated cefalexin dispersible tablets after oral administration to beagle dogs.