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doi: 10.1002/jcb.25078 82 ChoYAJueSSBaeWJHeoSHShinSIKwonIKet al

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In 428.101(a), CMS proposes to identify a Part D rebatable drug [580] for each applicable period by determining which covered Part D drugs, as defined in section 1860D-2(e) of the Act, meet the requirements in section 1860D-14B(g)(1)(C) of the Act (that is, are brand name drugs approved under an NDA, biologicals licensed under a biologics license application (BLA), or generic drugs approved under an ANDA)

We are requesting comments on these proposals, as well as information pertaining to potential clinician education for these proposed codes