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The FDA requires that generic drugs act as effectively and as fast as the initial brand name
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jeopardized to produce the products. Actually drugs are far only cheaper as the manufacturers
haven't experienced the expenses of marketing and developing a new medication. When a company
brings a new drug on the marketplace, the business has spent substantial money for
development, research, marketing and promotion. A patent is given that gives the business that
developed the drug an exclusive right to market the medication. Some times, generic versions
of a drug have different colors, tastes, or mixes of inactive ingredients compared to
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Trade mark laws in the United States don't allow the medication to check exactly like the
groundwork, but the active ingredients must be the exact same in both preparations, ensuring
both have the exact medicinal effects. Since the patent nears expiration, manufacturers can
apply to the FDA for permission to sell and make generic versions of their drug and minus the
startup costs for creation of their medication, other companies can afford to sell and make it
cheaply. The rivalry among them can also drive the price when multiple businesses begin
selling and producing a drug.
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