The chemical stability of drugs plays a pivotal role in the pharmaceutical industry, impacting drug development, manufacturing, storage, and ultimately, patient safety. This abstract explores the key aspects of chemical stability, emphasizing its significance in drug formulation and quality control. Chemical stability refers to a drug's ability to maintain its chemical composition and therapeutic efficacy over time, despite exposure to various environmental factors. Temperature, humidity, pH, light, and the presence of impurities are among the critical factors influencing a drug's stability. The deviation from stability can lead to decreased potency, changes in pharmacokinetics, and the formation of potentially toxic degradation products, posing risks to patients. Stability testing is a systematic process that assesses how different conditions affect a drug product over time. It employs analytical techniques to monitor changes in the drug's chemical and physical properties. These studies provide essential data for determining a drug's shelf life, recommended storage conditions, and appropriate packaging materials. The chemical stability of drugs is a fundamental element in pharmaceutical science, underpinning the quality, safety, and efficacy of medications. Rigorous stability testing is essential in drug development and regulatory approval, guaranteeing that patients receive safe and effective therapies. As the field continues to evolve, an enhanced understanding of drug stability contributes to the development of more durable, reliable pharmaceutical products.