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a preferred oral formulation thus preferably includes an effective amount of GSH mixed with a stabilizing agent, which is administered under such conditions that the concentration of GSH attained in the lumen of the latter portion of the duodenum is higher than the plasma GSH concentration, and preferably higher than the intercellular concentration of the epithelial lining cells

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(2) For a Part B rebatable drug first approved or licensed by the FDA after December 1, 2020, the benchmark period CPI-U is the CPI-U for the first month of the first full calendar quarter after a drug's first marketed date

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