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We refer readers to section IV.A.4.a.(1) of this proposed rule for the discussion of six additional proposed MVPs addressing a range of clinical conditions and specialty care

supply of product and significantly affects the manufacturer's ability to fill orders or meet expected demand for the generic Part D rebatable drug(s) or biosimilar(s) for at least 90 days

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Children such as younger siblings are at risk of experiencing nicotine effects from e-liquids and toxic aerosols through direct contact or through secondhand inhalation (Callahan-Lyon, 2014)