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Pharmaceutical tablet manufacturing is the process of producing tablets that contain medications or supplements in a controlled and standardized manner. The process typically involves several stages, including the preparation of the active pharmaceutical ingredient (API), formulation of the tablet, compression of the tablet, and final packaging.

During the preparation of the API, the raw materials are tested for purity and potency, and the chemical synthesis or extraction process is carefully monitored to ensure consistency and quality. The formulated tablet is then produced by mixing the API with other excipients, such as fillers, binders, and disintegrants, and compressing the resulting mixture into the desired shape and size.

Once the tablet is formed, it is inspected for defects, such as cracks or chips, and then packaged into blister packs or bottles with appropriate labeling and information. Quality control and assurance are critical components of pharmaceutical tablet manufacturing, with rigorous testing and analysis performed throughout the process to ensure that the final product is safe, effective, and consistent.