To Formulate and Evaluate Paracetamol Tablet

The present study aims to formulate and evaluate paracetamol tablets to ensure optimal therapeutic efficacy, safety, and patient compliance. Paracetamol, a widely used analgesic and antipyretic agent, was selected due to its well-established pharmacological profile and extensive clinical use. Tablets were prepared using the direct compression method with various excipients to enhance compressibility, disintegration, and dissolution profiles. The formulated tablets were evaluated for key quality parameters including hardness, friability, weight variation, disintegration time, and in vitro drug release. The results indicated that the optimized formulation met pharmacopeial standards and exhibited.