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The FDA requires that generic drugs act as fast as efficiently as the original products.
Generic drugs are copies of brand-name drugs that have the exact same dose, meant useeffects,
side effects, route of administration, risks, safety, and strength as the original drug. To
put it differently, their pharmacological effects are the same as the ones of their
counterparts. So there is no truth in the urban myths which generic drugs are manufactured
from facilities that are poorer-quality or are poor in quality to drugs. The FDA applies the
same standards for many drug manufacturing centers, and lots of businesses fabricate both
generic and brandname drugs. Actually, generic drugs are simply cheaper because the
manufacturers have not experienced the expenses of developing and selling a new medication.
When an organization brings a brand new drug onto the market, the business has spent
substantial money on research, development, marketing and promotion. A patent is given that
gives the company that acquired the medication an exclusive right to sell the medication.
Sometimes, generic versions of a drug have different colors, flavors, or combinations of
inactive ingredients than the first medications. Trade mark laws in the United States don't
allow the generic medication to look exactly like the brand-name groundwork, but the active
ingredients have to be the same in both preparations, ensuring both have the exact effects.
Because the patent nears expiration, manufacturers can apply to sell and make generic versions
of the medication and minus the startup costs for development of this drug, sell and other
companies are able to afford to make it. When companies begin producing and selling a drug,
your competition among them are able to drive the price. Lots of folks become concerned
because drugs are substantially less expensive than the brand-name variants.
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They wonder whether effectiveness and the high quality are jeopardized to create the more
affordable products.
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