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The whole manufacturing process is regulated by the US Food and Drug Administration (FDA) and other relevant authorities.

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A generic drug is actually its brand-name equivalent, although it doesnt bear the original trademark and looks slightly different.

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A generic drug simply means that the drug is not made by the original manufacturer, the chemical is exactly the same.

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Manufacturers of generic drugs cannot use brand names on their pharmaceuticals as that would be the breach of copyright while using the well known ingredients is absolutely legal.

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According to the recent FDA data, generic drugs account for about 45-50 percent of all prescription drug purchases in the United States.

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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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