West Virginia MPJE (Pharmacy Jurisprudence) Practice Exam

What information is required to be on unit-dose packaging?

1. Drug name, quantity of active ingredient, BUD, and lot number

2. Drug name, quantity of active ingredient, patient's name, and lot number

3. Drug name, quantity of active ingredient, pharmacist's name, and expiration date

4. Drug name, quantity of active ingredient, manufacturer's name, and patient's name

The correct answer is: Drug name, quantity of active ingredient, BUD, and lot number

The correct answer includes the essential elements that must be displayed on unit-dose packaging to ensure clarity and safety in medication administration. The inclusion of the drug name helps identify the medication being dispensed, which is crucial for both healthcare providers and patients. The quantity of the active ingredient is also vital, as it communicates the exact dosage present in each unit, helping to prevent potential dosing errors. In addition, the beyond-use date (BUD) is critical because it indicates until when the medication can be safely used, protecting patients from potential harm due to expired medications. The lot number is used to trace the medication back to its manufacturing batch, which is important for quality control and recall purposes if any issues arise with that particular batch. These components collectively ensure that the medication can be accurately administered and that any necessary information related to safety and tracking is readily available. Other options contain elements that, while relevant in different contexts, do not meet the specific requirements established for unit-dose packaging as comprehensively as the correct answer.