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The FDA requires that generic drugs work as efficiently and as fast as the unique brand name
products. Generic drugs are copies of brand name drugs that have the exact same dosage
effects, side effects, route of management, risks, safety, and strength because the original
medication. To put it differently, their pharmacological effects are the same as those of
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So there is no truth from the fables which generic drugs are manufactured from centers or are
inferior in quality. The FDA applies the very same standards for several medication
manufacturing facilities, and both brand name and generic medication are manufactured by
businesses. In fact, the FDA estimates that 50% of generic drug production is by companies.
Actually, generic drugs are far cheaper because the manufacturers haven't had the expenses of
marketing and developing a new medication. When a company brings a brand new drug onto the
current market, the firm has spent substantial money for promotion, development, marketing and
research of this medication. A patent is granted that gives an exclusive right to sell the
medication for as long as the patent is essentially. Generic versions of this drug have
various colors, flavors, or mixes of inactive ingredients compared to medications. Trademark
legislation in the United States do not allow the drugs that are generic to look exactly like
the preparation, but the active ingredients must be the same in both preparations, ensuring
both have the exact effects. As the patent nears expiration, manufacturers can apply to sell
and make generic versions of their medication and without startup costs for creation of their
medication, sell and other companies can afford to make it cheaply. When multiple companies
begin selling and producing a medication, the rivalry one of them is able to also drive the
price down further. Many people become concerned because drugs are often cheaper compared to
brandname variants. They wonder whether efficacy and the high quality are compromised to make
the products.
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