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To facilitate manufacturer understanding of the Preliminary Rebate Report, CMS is proposing in proposed 428.401(b)(1) that the Preliminary Rebate Report would include the following information: the NDC(s) for the Part D rebatable drug as defined under proposed 428.20

and (4) Reporting burden on MIPS eligible clinicians is significantly reduced

CMS understands it is possible that a manufacturer may not have sales or monthly units of a COD to report to the Medicaid Drug Programs system for a calendar quarter because, for example, there may be a temporary interruption in sales of the COD, or there may be no sales immediately after the drug is first approved or licensed by the FDA

These pack a much higher dose per session