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The FDA requires that generic drugs work as fast and as
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Generic drugs are copies of brand name drugs that have
exactly the same dosage effects, side effects. To put it
differently, their pharmacological effects are the same as
those of their brand-name counterparts. So there is no truth
in the fables that generic drugs are stated from poorer-
quality centers or are poor in quality to drugs. The FDA
applies the exact standards for many drug manufacturing
facilities, and both medication are manufactured by many
companies. Generic drugs are far simply cheaper because the
manufacturers never have experienced the expenses of growing
and marketing a new medication. When an organization brings a
brand new drug onto the current marketplace, the business has
spent substantial money for promotion, development, marketing
and research of the medication. A patent is given that gives
an exclusive right to sell the drug. Sometimes, generic
versions of this drug have tastes, various colours, or mixes
of inactive ingredients compared to medications. Trademark
legislation in the United States do not allow the medication
that are generic to look like the brand-name groundwork,
however the active ingredients have to be the same in both
preparations, ensuring that both have exactly the same
effects. Since the patent nears expiration, manufacturers can
apply to the FDA for permission to make and sell generic
versions of their medication and without startup costs for
development of the drug, additional companies are able to
afford to make and sell it. When companies begin selling and
producing a drug, the competition one of them is able to drive
the price. Many people come to be concerned because generic
drugs are substantially cheaper compared to brandname
variants. They wonder whether efficacy and the quality are
compromised to generate the products.