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The FDA requires that generic drugs act as fast as efficiently as the original brand-name
services and products. Generic drugs are copies of brandname drugs that have the exact same
dosage useeffects, side effects. To put it differently, their effects are the same as the ones
of these counterparts. So there is no truth in the myths that generic drugs are manufactured
from facilities that are poorer-quality or are inferior in quality to brand name drugs. The
FDA uses the exact standards for many drug manufacturing centers, and both generic and
brandname medication are manufactured by businesses. Generic drugs are far more economical
because the manufacturers never have experienced the expenses of selling and growing a new
medication. When a company brings a brand new drug onto the market, the firm has spent
substantial money for promotion, development, research and promotion. A patent is given that
gives an exclusive right to sell the medication for as long as the patent is in effect.
Generic versions of this drug have various colors, flavors, or mixes of ingredients compared
to medications that are initial. Trademark legislation in the United States do not permit the
generic medication to appear exactly like the 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 the drug and minus startup costs for development of this drug, sell
and additional companies are able to afford to make it cheaply.
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When multiple businesses begin selling and producing a drug, the rivalry among them is able
to drive the price. Many people come to be concerned because drugs are often cheaper than the
brand-name versions. They wonder if efficacy and the high quality are compromised to produce
the more affordable products.
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