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The FDA requires that generic drugs work as effectively and as fast as the authentic
brandname services and products. Generic drugs are copies of brandname drugs that have the
exact same dosage effects, side effects, route of administration, risks, safety, and strength
as the original drug. In other words, their effects are the same as those of their
counterparts. So there is not any truth from the urban fables that generic drugs are
manufactured from poorer-quality facilities or are inferior in quality. The FDA uses the same
standards for all medication manufacturing centers, and several companies manufacture both
drugs. In reality, the FDA estimates that 50 percent of generic drug production is by brand-
name businesses.
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Actually, generic drugs are cheaper as the manufacturers never have had the expenses of
developing and marketing a new drug. When an organization brings a new drug on the
marketplace, the business has spent substantial money on promotion, development, marketing and
research of this medication. A patent is granted that gives an exclusive right to promote the
medication. Some times, generic versions of a drug have various colors, flavors, or mixes of
inactive ingredients compared to medications. Trade mark laws in the USA do not permit the
drugs to look like the preparation, however the active ingredients have to be the exact same
in both preparations, ensuring both have the same medicinal effects. Because the patent nears
expiration, manufacturers can apply to sell and make generic versions of their medication and
without the startup costs for development of this medication, sell and other companies can
afford to make it. The competition among them is able to also drive the price, when multiple
companies begin producing and selling a drug. Many folks become concerned because drugs are
substantially less expensive compared to brand-name variants. They wonder whether the high
quality and efficacy are compromised to generate the products.
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