Differences between compounding and manufacturing

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Reference no: EM133595041

According to USP-NF Chapter <795>, how is compounding defined?
What are the major differences between compounding and manufacturing?
Name four reasons why it might be necessary to compound a preparation.
What reference might be used to aid in the compounding of a particular preparation? Why, what type of information does it contain?
How is compounding regulated in pharmacy?
Your pharmacy receives an order for a compounded preparation, what are your responsibilities as a compounder? What are the responsibilities of the pharmacists?
You work in a retail pharmacy and receive a prescription for a compounded preparation. Upon reviewing the order, the pharmacist asks you to preform the compounding. In the process, you determine that the pharmacy's stock of sucrose (table sugar) is too low to compound the quantity of the ordered prescription, but the store stocks sugar for customer purchase. Will you be able to use the sugar stocked by the store in the compounding process? Why/Why not?
Name the three main categories of instabilities.
What is the difference between an expiration date and beyond-use date?
What are the recommendations for assigning BUDs for non-sterile preparations?

Reference no: EM133595041

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