Method Development and Validation of Pregabalin in Bulk and Tablet Dosage forms by UV Spectroscopy

For determining Pregabalin in bulk and pharmaceutical formulations, a straightforward and accurate UVspectrophotometric method was created and verified. Distilled water was used as the solvent in the estimation. It wasdetermined that the absorbance was 210 nm. A correlation coefficient of 0.997 indicated that the method's range waslinear, between 2 and 10 μg/ml. 98.12–101.17% was the recovery rate determined. There was less than a 2-foldrelative standard deviation found. Assay, robustness, ruggedness, quantitation limit, accuracy, and precision were allevaluated in the validation process. It has been discovered that this UV spectrophotometric approach isstraightforward, exact, accurate, repeatable, and reasonably priced. In the bulk and pharmaceutical formulationssectors, the method can be helpful for routine daily analysis carried out by quality control departments.