Search for: "AVENTIS PHARMACEUTICALS, INC.," Results 21 - 40 of 219
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30 Jan 2020, 10:49 am by luiza
In January 2019, Illinois reached a $135 million settlement with Teva Pharmaceuticals, and in October, the state reached a $242 million settlement with more than a dozen different drug makers, including Abbot Laboratories, Aventis, GlaxoSmithLine, Johnson & Johnson, McNeil, Novartis, and more. [read post]
1 Aug 2019, 8:30 am by Seeger Weiss LLP
Boehringer Ingelheim Corp., et al., a $150 million settlement with GlaxoSmithKline PLC, and a $190 million settlement with Aventis Pharmaceuticals, Inc. [read post]
5 Feb 2018, 9:59 pm by Patent Docs
Mylan Pharmaceuticals, Inc. v. [read post]
5 Sep 2017, 7:45 am by Ben Vernia
According to DOJ’s press release: Pharmaceutical companies Mylan Inc. and Mylan Specialty L.P. have agreed to pay $465 million to resolve claims that they violated the False Claims Act by knowingly misclassifying EpiPen as a generic drug to avoid paying rebates owed primarily to Medicaid, the Justice Department announced today. [read post]
25 Aug 2017, 7:02 am by Fraud Fighters
On Thursday, August 17, 2017, the Department of Justice, announced that Mylan Inc. and Mylan Specialty L.P. [read post]
25 Aug 2017, 7:02 am by Fraud Fighters
On Thursday, August 17, 2017, the Department of Justice, announced that Mylan Inc. and Mylan Specialty L.P. [read post]
10 Oct 2016, 2:59 pm by Michael Grossman
Taxotere: The Case Against a Chemo Drug Taxotere, the marketed brand name of the drug docetaxel, is a taxane-class drug manufactured by Sanofi-Aventis Pharmaceutical. [read post]
26 Jul 2016, 8:45 pm by Patent Docs
Zydus Pharmaceuticals (USA) Inc. 1:16-cv-00540; filed June 29, 2016 in the District Court of Delaware Plaintiffs: Genzyme Corp.; Sanofi-Aventis U.S. [read post]
29 Jul 2015, 10:00 pm by Courtenay C. Brinckerhoff
LLC and Regeneron Pharmaceuticals, Inc. filed a petition for Inter Partes Review (IPR) of the “Cabilly II” patent, U.S. [read post]
26 May 2015, 7:42 am
  Claims such as in Mills, which are at loggerheads with FDA criteria for drug development, are precisely those with the most potential for making pharmaceutical manufacturers into “sitting ducks” for litigation, in this instance litigation based on extraneous genetic factors.It may well be that the coming (and to some extent existing) revolution in genetically individualized medical therapy will require changes in how drugs are evaluated, labeled, etc., but this is a… [read post]
17 May 2015, 4:00 am by Administrator
Pharmaceuticals: Amending PleadingsSanofi-Aventis v. [read post]