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The official website of the Federal Trade Commission, protecting America’s consumers for over 100 years. ... The complaint charges that Cephalon was able to induce each of the generic companies to abandon its patent challenge and agree to refrain from selling a generic version of Provigil until 2012 by agreeing to pay the companies a total ...
FTC Sues Cephalon, Inc. for Unlawfully Blocking Sale of Lower-Cost Generic Versions of Branded Drug Until 2012 Complaint Charges Company Paid Four Generic Drug Makers in Order to Protect Monopoly Profits on its Leading Product
Apr 28, 2008 · The FTC filed this action on February 13, 2008. Although the complaint alleges violations of Section 13(b) of the Federal Trade Commission Act, 15 U.S.C. § 53(b), the action is premised upon the same operative facts and events that form the basis for the private Sherman Act cases pending in the Eastern District of Pennsylvania.
Jun 19, 2015 · The FTC’s complaint alleged that Cephalon’s settlements constituted unfair methods of competition in violation of Section 5(a) of the FTC Act, 15 U.S.C. § 45(a). The complaint sought an injunction prohibiting Cephalon from enforcing terms of the agreements that barred the generic manufacturers from marketing generic versions of Provigil ...
Jan 25, 2017 · On January 18, 2017, the U.S. Federal Trade Commission (FTC) and the Attorneys General of Alaska, Maryland, New York, Texas, and Washington filed a complaint in federal district court for the District of Columbia seeking a permanent injunction and other equitable relief against Mallinckrodt ARD Inc. and Mallinckrodt plc (Mallinckrodt) for unfair methods of competition in violation of Section 5 ...
N. "FTC Action" means FTC v. Cephalon, Civil Action no. 2-08-cv-2141-MSG. 0. "FTC lnjuµction" means the Stipulated Revised Order for Pennanent Injunction and ... to act set forth or alleged in the proposed Complaint filed·by California as part of implementing this Settlement Agreement ("Complaint"), including, without
reports by the Federal Trade Commission (FTC) indicate that generic versions of as many as 142 brand-name drugs have been delayed by pay-for-delay arrangements between drug manufacturers since 2005.1 However, because the details of these deals rarely become public, consumers have largely been kept in the dark about the extent of the problem.
FTC v. Cephalon, Inc. (Provigil) 2009 – private litigation filed 2014 – FTC complaint filed 2016 – discovery substantially completed . Summary judgment hearing scheduled
May 29, 2015 · Teva Settles Cephalon Generics Case With F.T.C. for $1.2 Billion. ... The Federal Trade Commission said its seven-year lawsuit against the drug ... according to the F.T.C. complaint …
By Christopher Norton. Law360 (July 28, 2009, 5:38 PM EDT) -- A judge on Tuesday asked for all motions to be refiled in the Federal Trade Commission's ongoing antitrust suit alleging Cephalon Inc ...
A Pennsylvania federal judge on Wednesday approved the Federal Trade Commission's record-setting $1.2 billion settlement with Cephalon Inc. in a long-running antitrust suit accusing the company of ...
Feb 23, 2019 · Although Teva is currently bound by a prior order in FTC v. Cephalon, the new order is broader, prohibiting Teva from entering into the two most pernicious and common forms of …
Provigil: A Case Study of Anticompetitive Behavior by MICHAEL A. CARRIER* I. Introduction Using the sleep-disorder drug Provigil as a case study, this article exposes a new type of anticompetitive harm that stems from the combination of two distinct activities. First, brand-name drug firms
FTC v. Cephalon (E.D. Pa.) Complaint filed in February 2008. The FTC survived Cephalon’s motion to dismiss and discovery completed FTC v. Watson (N.D. Ga.) Complaint filed in January 2009. After the case was transferred from C.D. Ca. to N.D. Ga., the FTC lost on Defendants’ motion to dismiss.
The third case involves a generic drug manufacturer, Apotex, who has raised non-infringement and patent invalidity allegations, as well as antitrust claims in Apotex, Inc. v. Cephalon, Inc., et al., 2:06-cv-2768.5 Finally, the Federal Trade Commission (hereainfter "F.T.C.") has …
Last year in a landmark decision, the Supreme Court ruled that pharmaceutical “reverse payment” settlements in Hatch-Waxman Act “Paragraph 4” patent litigation are subject to challenge, departing from the rule that most Circuits had adopted. FTC v. Actavis , 133 S.Ct. 2223 (2013).
On June 17, 2015, the U.S. District Court for the Eastern District of Pennsylvania approved a consent order (the Consent Order) between the Federal Trade Commission and defendants Cephalon, Inc. and its parent, Teva Pharmaceutical Industries Ltd.,  resolved long-running antitrust litigation stemming from four reverse payment settlements of Hatch-Waxman patent infringement cases involving ...
Jan 30, 2017 · The FTC's Complaint stated that Acthar is the only therapeutic adrenocorticotropic hormone (ACTH) product sold in the U.S. ACTH is the primary drug used to treat infantile spasms (IS) ... See Statement of the Federal Trade Commission, FTC v. Cephalon, Inc. (May 28, 2015). 30.
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