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The FDA requires that generic drugs work as fast as efficiently as the authentic services and
products. Generic drugs are copies of brand name drugs which have the exact same dosage usage
, effects, side effects. In other words, their effects are the same as those of their
counterparts. So there is no truth from the urban fables generic drugs are manufactured in
facilities or are poor in quality which. The FDA applies the same standards for many drug
manufacturing facilities, and both brand-name and generic drugs are manufactured by
businesses. Generic drugs are far more economical because the manufacturers never have
experienced the expenses of marketing and growing a new medication. When a company brings a
brand new drug on the marketplace, the firm has spent substantial money on promotion,
development, research and promotion of their medication. A patent is given that gives a unique
right to promote the drug to the company that developed the drug. Generic versions of this
drug have different colours, tastes, or combinations of inactive ingredients than the
medications that are initial. Trademark laws in the United States do not allow the generic
medication to look like the preparation, but the active ingredients must be the exact 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 the startup costs for development of this drug, other
businesses can afford to make and sell it. Your competition one of them is able to also drive
the price down further when multiple businesses begin selling and producing a drug. Many men
and women come to be concerned because drugs are often cheaper than the brand-name variants.
They wonder whether the high quality and effectiveness have been jeopardized to create the
more affordable products.
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