A generic drug is the same as it’s brand name counterpart, but is much less expensive usually. A generic drug must have the same active ingredients, path of administration, dosage where to buy in canada, kewvineyards.com, form, power, and indications as the original brand product. Generic medications are authorized by the U.S. Drug and Food Administration, and so are deemed to end up being as effective and safe as the brand product.
Generics can’t be sold until after the drug patent expires on the initial brand name product. For instance, generic fluoxetine could not be sold before patent had expired on the brand equivalent Prozac. A medication manufacturer applies tablets for sale a patent to safeguard their medication from getting copied and over the counter drugs (http://kewvineyards.com/pharmacy/lopressor) offered by another firm and losing profits.
Patents expire twenty years from the date of filing typically. During this period of patent protection, only the original manufacturer can analysis, develop and sell the brand medication. When the patent expires, other producers can send an abbreviated new drug program (ANDA) to the FDA for acceptance to market the generic version.
Generic drugs have lower research costs and improved market competition and those substantial savings are passed on to the patient. However, generic drugs must meet tight FDA requirements with respect to quality still, performance, labeling, manufacturing, and bioequivalence. For legal reasons, generic drugs must have the same substances as the brand product, and they should be expected to really have the same impact when found in place of a brand name drug.
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