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As is also discussed in section 50, CMS considered options for establishing a standardized method and process at regular intervals to determinate any appropriate adjustments to the rebate amount for a Part D rebatable drug for an applicable period to account for additional revised information as well as options for recalculation based on CMS identifying an agency error or determining manufacturer data was misreported

the drug can be deposited on surfaces through e-cigarette vapor, according to the American Chemical Society