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Heres what you need to know about the evolving market, growing safety concerns, and new regulatory efforts: To view or add a comment, sign in The FDA's statistical formula that defined bioequivalence as a range---a generic drug's concentration in the blood couldn't fall below 80% or rise above 125% of the brand names's concentration, using a 90% confidence interval---still allowed for a potential outside range of 45% among generics labelled as being the same
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