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We also proposed new policies for the Medicare Part D Drug Inflation Rebate Program as follows: Proposed 428.202(c)(3) provided that if a Part D rebatable drug first approved or licensed by the FDA on or before October 1, 2021, does not have AMP data reported under section 1927(b)(3) of the Act for any quarters during the period beginning on January 1, 2021 and ending on September 30, 2021, CMS will identify the payment amount benchmark period as the first calendar year, which would be no earlier than calendar year 2021, in which such drug has at least 1 quarter of AMP reported

Although there appears to be only one GS gene (Webb et al ., 1995), there are two forms of the disease (Ristoff and Larsson, 1998): a milder form, caused by a GS deficiency limited to erythrocytes, resulting in chronic haemolytic anaemia and neonatal jaundice

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