GENERIC DRUG?
Jun 15, 2023
The FDA (U.S. Food and Drug Administration) approves generic medicines based on a thorough evaluation of their safety, efficacy, and quality. The generic drug approval process involves demonstrating bioequivalence to the brand-name drug and meeting the FDA's stringent regulatory standards.
It's important to note that generic drugs approved by regulatory authorities outside the United States may have undergone similar evaluations by their respective regulatory bodies. Different countries may have variations in their approval processes, but they generally ensure that generic drugs meet established standards of safety, efficacy, and quality.
The FDA's approval process for generic medicines helps ensure that patients have access to safe, effective, and affordable alternatives to brand-name drugs.
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