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Question
which of the following information should a pharmacy technician include on the compounding record for a non-sterile compound?
prescriber information
dosage instructions
date of compounding
stability information
Identify the regulatory requirements
Using the USP 795 Regulations and Nonsterile Compounding knowledge points
- USP Chapter <795> governs the standards for nonsterile compounding in pharmacies.
- A compounding record (CR) is an individual record that documents the actual preparation of a specific compounded preparation.
- According to USP <795>, the compounding record must include specific details of the compounding process to ensure traceability and quality control.
Evaluate the options
Using the USP 795 Regulations knowledge point
- Prescriber information and Dosage instructions are typically found on the prescription label or master formulation record, but are not standard requirements for the internal compounding record itself.
- Stability information is generally part of the Master Formulation Record (MFR) rather than the individual batch compounding record.
- Date of compounding is a mandatory element of the compounding record to document exactly when the preparation was made, along with the assigned beyond-use date (BUD), the names of the individuals who compounded and verified the preparation, and the specific lot numbers of the ingredients used.
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- Prescriber information
- Dosage instructions
- Date of compounding (Correct answer)
- Stability information