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While generic drugs that do not meet the sole source criteria in section 1860D-14B(g)(1)(C)(ii) of the Act (that is, multiple source generic drugs) are excluded from the definition of a Part D rebatable drug, CMS understands that a generic drug may meet the definition of a Part D rebatable drug on the first day of an applicable period and then cease to meet such definition later in the applicable period if, for example, the FDA approves another therapeutically equivalent generic drug under a 505(j) ANDA and that drug is marketed during such applicable period

We will provide another update at 10:00 am EST on Saturday, September 27, 2025

Now, the USFWS has until November 2026 to issue a new environmental impact statement and decision on the matter

And e-cigs are becoming banned in more and more settings