Which information is required on repackaged containers?

When it comes to repackaged containers in the pharmacy setting, specific labeling requirements are mandated to ensure the safe and effective use of medications. The correct answer highlights that both the manufacturer and lot number must be included on repackaged containers. This information is critical for several reasons.

Firstly, the manufacturer's name provides traceability to the source of the drug, which is essential for quality assurance and safety monitoring. If there were to be a product recall or if a question arises regarding the drug's safety, knowing its manufacturer can help healthcare professionals and patients quickly access relevant information.

Secondly, the lot number is key for identifying the specific batch from which the drug was taken. This is particularly important in the event of adverse reactions or contamination, as it can direct investigations to the exact product lot.

Together, the inclusion of the manufacturer and lot number on repackaged containers supports proper medication management, assists in tracking drugs, and enhances patient safety by allowing for quick action when necessary. Other options, while related to drug labeling, do not encompass the essential details required for repackaged pharmaceuticals as defined by regulations.