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The FDA requires that generic drugs act as effectively as fast as the original brand name
products. Generic drugs are copies of brand-name drugs that have the exact same dose, planned
usage , effects, side effects. To put it differently, their pharmacological effects are the
same as the ones of their brand-name counterparts. So there is no truth from the myths that
generic drugs are manufactured in poorer-quality facilities or are poor in quality. The FDA
applies the very same standards for many medication manufacturing facilities, and both generic
and brand name drugs are manufactured by many companies. Actually, generic drugs are simply
cheaper because the manufacturers haven't experienced the expenses of developing and selling a
new medication. When an organization brings a new drug on the marketplace, the business has
spent substantial money on promotion, development, research and promotion of the medication.
There is A patent granted that gives the organization that developed the drug an exclusive
right to sell the medication for as long as the patent is in effect. Generic versions of this
drug have different colors, tastes, or mixes of ingredients compared to medications that are
initial. Trade mark legislation in the USA don't permit the generic medication to look exactly
like the preparation, but the active ingredients must be the same in both preparations,
ensuring both have exactly the exact medicinal effects. As the patent nears expiration,
manufacturers can apply to make and sell generic versions of their medication and minus the
startup costs for development of the medication, additional companies can afford to make and
sell it cheaply. When multiple companies begin selling and producing a drug, the rivalry among
them is able to also drive the price down further. Lots of people become concerned because
drugs are often cheaper compared to brandname variants. They wonder if the quality and
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