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Smoking-related toxicant exposure was also reduced, with CEMA and other toxicant levels comparable in combusted tobacco users as compared to users of both combusted and non-combusted tobacco

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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)