The Hatch-Waxman Act allows a generic drugmaker to rely on a branded drugmaker’s Food and Drug Administration-approved New Drug Application if the generic drugmaker can show that the.
In Mentone Solutions LLC v. Digi International Inc., 2021 WL 5291802 (Fed. Cir. Nov. 15, 2021) the U.S. Court of Appeals for the Federal Circuit reversed the U.S. District Court for the.
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