Which aspect of tablets is ensured by control procedures in non-sterile compounding?

The correct answer focuses on the importance of ensuring that each tablet produced during non-sterile compounding is uniform in size and remains intact. Control procedures in compounding aim to guarantee that each dosage form meets specified standards for quality and consistency. Uniformity in size is crucial because it directly impacts the dosage accuracy and therapeutic effect of the medication. If tablets vary significantly in size, it could lead to inconsistencies in drug delivery and effectiveness, which could have serious ramifications for patient safety.

Quality control measures during the tablet compounding process verify that each tablet adheres to the predetermined specifications for size and structural integrity. This not only includes checking for proper weight and dimensions but also ensuring that each tablet remains whole without any breakage or crumbling, which could affect both dosing and patient compliance.

While flavor uniformity and color consistency may be considered in some formulations, they are not as critical as size and integrity concerning the therapeutic outcomes. Checking solely for texture would not encompass the comprehensive quality control that is vital for patient safety and efficacy. Thus, the emphasis is rightly placed on the uniformity in size and intactness of the tablets.