Ohio Pharmacy Law Practice Test

What information must labels contain for repackaged drugs stored within a pharmacy prior to being dispensed?

1. Drug's price and origin

2. Drug's name, strength, and dosage form

3. Manufacturer's contact information

4. Pharmacy's hours of operation

The correct answer is: Drug's name, strength, and dosage form

The requirement for repackaged drugs to have labels that include the drug's name, strength, and dosage form is rooted in ensuring safe and effective medication use. This information is crucial for both pharmacists and patients because it allows for the accurate identification of the medication. The drug's name ensures that there’s no confusion about the medication's identity, while the strength informs the user about the potency of the drug that has been repackaged. The dosage form indicates how the drug is administered (e.g., tablet, capsule, liquid), which is essential for ensuring that patients receive the medication in the manner intended. This labeling standard is a key component of pharmacy law and ensures compliance with safety regulations. It supports pharmacists in preventing medication errors and aids patients in understanding the medication they are receiving, thus promoting better adherence and health outcomes.