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We stated in the proposed rule that we continued to be interested in comments on this topic and thus welcomed additional comments on this approach and alternative approachesspecifically, how CMS should address the situations in which the manufacturer of a Part D rebatable drug does not have an MDRP agreement in effect for any part of the applicable period or when a Part D rebatable drug may be excluded from the definition of a COD and manufacturers may not be required to report pricing and drug product information under section 1927(b)(3) of the Act