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26 Dec 2011, 12:37 pm by Steve McConnell
Actavis Totowa, LLC, 2009 WL 1082026 (N.D. [read post]
24 Feb 2011, 1:49 pm by Bexis
Actavis Totowa, LLC, 2010 WL 3604674, at *3-4 (S.D. [read post]
31 Dec 2009, 2:34 am by Sean Wajert
Actavis Totowa, LLC, et al., 2:08-cv-01282  • William J. [read post]
29 Oct 2009, 3:13 am
Dozens of product liability cases alleging that defendants Actavis Totowa LLC, Actavis Inc. and Actavis Elizabeth LLC marketed Digitek tablets containing double the appropriate dosage were transferred to an MDL assigned to Chief Judge Goodwin of the Southern District of West Virginia last summer. [read post]
28 Sep 2009, 1:31 am
We received a copy of Ford Motor Co. v. [read post]
28 Sep 2009, 1:31 am
We received a copy of Ford Motor Co. v. [read post]
28 Sep 2009, 1:31 am
We received a copy of Ford Motor Co. v. [read post]
24 Sep 2009, 5:09 am
We received a copy of Ford Motor Co. v. [read post]
8 May 2009, 12:10 am
Actavis Totowa LLC, 2009 WL 1082026 (N.D. [read post]
21 Apr 2009, 2:34 am
A similar massive recall was announced by Actavis Totowa LLC, Mylan Bertek and UDL on April 25, 2008, involving millions of pills that were improperly manufactured at a facility in Little Falls, New Jersey, which has been the subject of much controversy and a Congressional inquiry. [read post]
14 Nov 2008, 3:23 pm
Department of Justice (DOJ)  issued a Press Release concerning the court papers  that were  filed against Actavis Totowa LLC, "U.S. [read post]
4 Nov 2008, 6:18 am
Digitek, also known as digitalis or digoxin, is a prescription drug that was recalled from the market in April of 2008 by manufacturers Actavis Totowa, LLC; Actavis, Inc.; Actavis US; Mylan, Inc.; Mylan Pharmaceuticals, Inc.; Mylan Laboratories, Inc.; Mylan Bertek Pharmaceuticals; and UDL Laboratories, Inc. [read post]
16 Oct 2008, 7:17 pm
As you may know already, in April 2008 Actavis Totowa LLC recalled all strengths of Digitek due to the possibility that tablets with double the appropriate thickness may contain twice the approved level of active ingredient. [read post]
9 Oct 2008, 3:59 pm
Dingell and Stupak sent a letter to FDA Commissioner Andrew C. von Eschenbach to inform him that Congress will investigate the facts giving rise to the Class 1 recall of Digitek in the spring of 2008 as well as the August 1, 2008 recall of all generic drugs manufactured at the Actavis Totowa LLC at its plant in Little Falls, New Jersey (formerly operated by Amide Pharmaceuticals). [read post]
26 Sep 2008, 7:23 pm
Furthermore, on August 1, 2008 Actavis Totowa LLC announced a recall of all generic drugs manufactured at its Little Falls plant, apparently due  to a lack of good manufacturing practices (GMP) and/or a lack of quality control at this particular New Jersey facilty. [read post]
14 Aug 2008, 2:32 am
Sixty-five different potentially dangerous generic drugs manufactured by Actavis Totowa, LLC, one of the world's largest generic drug manufacturers, were recalled from market last week. [read post]