Are there any laws governing the use of generic drugs?
Yes, there are laws governing the use of generic drugs in California. All generic drugs must be approved by the U.S. Food and Drug Administration (FDA) to ensure they are equivalent to their brand-name counterparts. California requires that generic drugs must meet the same standards as brand-name drugs, including safety, quality and efficacy. In addition, drug manufacturers are required to provide complete information about generic drugs to the FDA and to the public. This information must include the active ingredient, dose, route of administration, indications, and strength. Furthermore, drug manufacturers must follow good manufacturing practices, which ensure that the medicines made are safe and effective for patients. Generic drugs are also subject to California’s prescription drug monitoring program. This program helps to detect, prevent, and regulate the inappropriate use of prescription drugs. It also requires pharmacies to report all sales of prescription drugs to a state-run database. Finally, California’s generic drug substitution law allows pharmacists to substitute generic drugs for their brand-name counterparts. As long as the generic drugs are approved and equivalent to their brand-name counterparts, pharmacists can dispense generic drugs even when a physician has prescribed a brand-name drug.
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