What did the Drug Listing Act of 1972 require for each new medication?

The Drug Listing Act of 1972 established the requirement for a National Drug Code (NDC) number to be assigned to each new medication. The NDC serves as a unique identifier that provides essential information about the drug, including the manufacturer, product, and package size. This coding system helps ensure the accurate identification and tracking of drugs, facilitating proper regulation and safety monitoring.

The introduction of the NDC system enhances the efficiency of drug information processing and aids in inventory management, billing, and prescription writing. It is critical for pharmacists and healthcare providers as they manage and dispense medications, ensuring that they can quickly access vital drug information.

The other options, while important components of pharmaceutical management, do not specifically pertain to the requirements set forth by the Drug Listing Act of 1972. They may be involved in various regulations surrounding medication safety and efficacy but are not mandated by this particular act.