Which is true about medications labeled for unit doses?

Medications labeled for unit doses are indeed required to include the manufacturer's information. This is crucial because such information ensures traceability and accountability throughout the distribution and administration process. It provides essential details about the medication, such as the active ingredients, dosing information, and potential side effects, which are vital for healthcare providers when administrating the medication to patients. Including the manufacturer's information also aids in identifying authenticity and recalls if necessary.

The other options do not accurately represent the characteristics of unit dose medications. For example, while they can be generic or brand-name products, they are not limited to generics. Additionally, unit doses are not generally classified as repackaged medications for mass distribution; instead, they are often prepared specifically for individual patient doses in hospitals or nursing facilities. Lastly, the use of unit dose medications depends on a valid prescription, meaning they cannot be distributed for use by any patient without proper authorization.