generic drug regulations

Generic drug regulations ensure that medications with the same active ingredients, strength, and dosage as brand-name drugs are safe, effective, and of high quality. Regulatory agencies like the FDA review and approve generics by confirming they meet strict standards, including bioequivalence—meaning they work the same way in the body. Generics are typically sold at lower prices because they don’t have the same development costs as brand names. These rules help protect consumers by ensuring that generic medicines are reliable alternatives, providing affordable options without compromising safety or effectiveness.