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Description

Fukuda H, Takekuma M, Hirashima Y Internal medicine (Tokyo, Japan) 2020

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Section 1847A(i)(1)(A) of the Act requires the Secretary to provide a report to each manufacturer of a Part B rebatable drug with the following information not later than 6 months after the end of an applicable calendar quarter: (1) the total number of billing units for each Part B rebatable drug

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