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The U.S. Food and Drug Administration (FDA) has approved Xanax for two primary conditions: generalized anxiety disorder (GAD) and panic disorder. GAD is characterized by persistent, excessive worry about everyday activities or events, often accompanied by physical symptoms such as fatigue, difficulty concentrating, irritability, and muscle tension. Xanax provides short-term relief by reducing the intensity and frequency of these symptoms. Panic disorder, the second FDA-approved use, involves sudden episodes of intense fear accompanied by physical symptoms like chest pain, rapid heartbeat, trembling, sweating, dizziness, and shortness of breath. These episodes can occur unexpectedly or in response to specific situations. Xanax can help reduce the severity of panic attacks and improve daily functioning during acute phases. However, because Xanax carries a risk of dependence and tolerance, healthcare providers use it cautiously and monitor patients closely. They may prescribe it during the initial stages of treatment while long-term therapies—such as cognitive-behavioral therapy or antidepressants—are being established. The FDA approval does not mean Xanax is appropriate for everyone. Individuals with a history of substance misuse, respiratory disorders, or certain medical conditions may require modified treatment approaches. Side effects, including drowsiness, memory issues, and impaired coordination, must also be monitored. The FDA emphasizes that Xanax should be taken exactly as prescribed and never shared with others. Education on safe use, interactions, and proper storage is essential to prevent accidental ingestion or misuse. While Xanax remains a valuable treatment when used appropriately, it must be part of a comprehensive, medically supervised plan for managing anxiety or panic disorder.