FDA & Generic Drugs
FDA defines generic
drugs: A generic drug is an identical or an
equivalent of a brand name drug in its dosage form, safety,
strength, quality, performance, characteristics and usage. Although
generic drug is identical to its branded counterparts, it is
typically sold at prices that are much lower than its counterparts'.
Figures from the Congressional Budget Office show
that generic drugs save consumers an estimated US$8 - US$10
billion a year. Hospitals are already using generic drugs
as their prescribed drugs and are rapidly pushing brand name
drugs out of the medical scene.
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