Which USP chapter deals with non-sterile compounding?

Chapter 795 of the United States Pharmacopeia (USP) specifically addresses non-sterile compounding, outlining the standards and guidelines necessary for pharmacists to follow when preparing non-sterile drug products. This chapter emphasizes the need for proper handling, compounding techniques, and quality control measures to ensure that non-sterile compounded preparations are made safely and effectively for patients.

The importance of this chapter lies in its focus on ensuring that compounded medications meet appropriate quality standards. It provides detailed instructions on various factors such as facilities, equipment, personnel qualifications, and the procedures to be followed, thereby helping to prevent contamination and ensure the stability of the compounded products.

In contrast, other chapters like Chapter 800 pertain to hazardous drugs and describe the practices required to ensure safety when handling such substances. Chapter 707 deals with the performance requirements for pharmacy compounding, particularly concerning compounded sterile preparations, while Chapter 1045 is focused on the stability of compounded sterile preparations. Each of these chapters discusses different aspects of compounding, but Chapter 795 is uniquely dedicated to non-sterile compounding, making it the correct choice for this question.