True or False: In an institutional setting, unit-of-use packages are legally labeled if they contain identification, drug name, strength, and expiration date.

In an institutional setting, unit-of-use packages must meet specific labeling requirements to be legally compliant. While identification, drug name, strength, and expiration date are essential components, there are additional requirements that must be fulfilled for the packaging to be considered legally labeled.

For a unit-of-use package to be compliant, it typically needs to include information such as the manufacturer's name, lot number, and dosage instructions. The absence of any of these critical details means that the package may not meet the legal standards established for pharmaceutical labeling. Therefore, stating that unit-of-use packages are legally labeled simply based on the presence of the identification, drug name, strength, and expiration date is insufficient, making the assertion false.

Understanding this helps clarify the broader context of pharmaceutical regulations, emphasizing the importance of comprehensive labeling for both patient safety and legal compliance.