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At 428.201(b), we proposed to exclude from the calculation performed under subpart C drugs and biologicals that meet the definition of a Part D rebatable drug, but which are missing AMP data for the entire duration of the applicable period because, for the reasons specified below, there were no quarters during that period in which their manufacturers were required to report AMP data under section 1927(b)(3) of the Act

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Acknowledgements This work was supported by the National Research Development and Innovation Office (NKFIH) grants (KKP 126963 awarded to A.R., NKFIH-PD-135121 awarded to M.B., NKFIH-PD-146252 awarded to D.C., and NKFIH-K-142486 awarded to I.P.), VEKOP-2.3.3-15-2016-00011, and by the Hungarian Academy of Sciences (KEP-10/2019), and by the National Research, Development and Innovation Fund (2020-1.1.2-PIACI-KFI-2020-00021 awarded to K.M.)