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The FDA requires that generic drugs act as fast as efficiently as the authentic services and
products. Generic drugs are copies of brand-name drugs that have the exact same dosage
effects, side effects. In other words, their effects are the same as the ones of these brand-
name counterparts. Therefore there is no truth in the myths which generic drugs are
manufactured in poorer-quality centers or are poor in quality. The FDA uses the same standards
for all medication manufacturing centers, and many companies manufacture both brand name and
generic drugs. In reality, the FDA estimates that 50 percent of generic drug production is by
brand name companies.
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Many men and women become concerned because generic drugs are often cheaper than the
brandname versions. They wonder if the quality and effectiveness are compromised to make the
products. Actually drugs are far cheaper because the manufacturers never have experienced the
expenses of developing and selling a new drug. When a company brings a brand new drug on the
market, the business has already spent substantial money for promotion, development, research
and promotion of their medication. A patent is given that gives a special right to sell the
medication so long as the patent is in effect to the company that acquired the medication.
Some times, generic versions of this drug have tastes, different colors, or combinations of
inactive ingredients compared to original medications. Trade mark legislation in the United
States do not permit the generic drugs to appear like the product groundwork, however the
active ingredients have to be the same in both preparations, ensuring that both have exactly
the exact effects. Whilst the patent nears expiration, manufacturers can apply to make and
sell generic versions of the drug and minus startup costs for development of the drug, other
businesses are able to afford to make and sell it. Your competition among them is able to
drive the price, when multiple companies begin producing and selling a drug.
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