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To put it differently generics have identical active ingredients and their pharmacological effects are the same, as those of their brand-name equivalents.
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A nonprescription, or over-the-counter (OTC) drugs, is one which the U.S. Food and Drug Administration (FDA) has found to be protected and efficient for direct client use based on the label directions and warnings. FDA requires a wider margin of safety for OTC medicines than for pharmaceuticals.
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