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Also provided herein is a process for preparing a stable oral liquid formulation comprising lisinopril, xylitol, a buffer, and sodium benzoate, the process which comprises the step of adding about 086 mg/ml anhydrous citric acid, about 144 mg/ml anhydrous sodium citrate, about 080 mg/ml sodium benzoate, about 109 mg/ml lisinopril dihydrate, and about 150 mg/ml xylitol to water; adjusting the volume to the desired volume by adding more water; and adjusting the pH to 49 by adding sodium hydroxide or hydrochloric acid.

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