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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)

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Its a defiant declaration of independence from the pressures to conform to industry standards, and instead, embracing a pure, unadulterated form of self-expression: rock

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