1Student,
2Assistant Professor,
This review paper presents a comparative analysis of the quality control measures applied to commercial ibuprofen tablets versus a formulated version of ibuprofen tablets. The study aims to evaluate the physicochemical properties, dissolution profiles, and overall efficacy of both formulations. By assessing parameters such as hardness, disintegration time, and dissolution rates, we aim to determine the quality and reliability of commercially available ibuprofen compared to a laboratory-formulated Tablet. The findings suggest significant differences in quality control metrics, which could have implications for clinical efficacy and patient safety. This study evaluates the physicochemical properties, disintegration times, dissolution profiles, and overall quality attributes of both formulations. The findings reveal significant differences in quality control parameters, emphasizing the importance of rigorous quality assessments in pharmaceutical manufacturing to ensure therapeutic efficacy and patient safety.
Ibuprofen Tablets, Formulation, In process quality control, Film-coated tablets, Tablet evaluation