Tag: Pharmaceutical law

In the United States, drugs are classified into five schedules based on their medical use and potential for abuse, with Schedule II and Schedule III drugs having distinct characteristics. This guide addresses the common question, **What are Category 2 and 3 drugs?**, by explaining the official DEA classifications and the critical differences between them.

Originating from the Durham-Humphrey Amendment of 1951, **what is a legend drug** became a crucial distinction in U.S. pharmaceutical law, mandating a prescription for specific medications. This legislative act was designed to ensure patient safety by restricting access to drugs with potential for harm, addiction, or misuse, distinguishing them from freely available over-the-counter options.