The legal library gives you easy access to the FTC’s case information and other official legal, policy, and guidance documents.
Federal Trade Commission Comment Before the Federal Communications Commission Regarding the Privacy and Security Practices of Broadband Providers and Their Impact On Broadband Adoption
20141525: AutoZone, Inc.; Dr. Karl Gaertner
20141531: Loews Corporation; Chevron Corporation
20141532: Crown Finance Foundation; Windjammer Senior Equity Fund III, L.P.
20141533: Michael S. Smith; ZHA FLNG, LLC
20141534: Lexington Capital Partners VIII, L.P.; Citigroup Inc.
20141539: Sinclair Broadcast Group, Inc.; James E. Rogers Trust
20141540: Calpine Corporation; Exelon Corporation
20141542: Arthur T. Demoulas; Demoulas Super Markets, Inc.
20141543: Frances Irene Demoulas; Demoulas Super Markets, Inc.
20141545: TAD Family Trust; Demoulas Super Markets, Inc.
20141546: Caren L. Demoulas; Demoulas Super Markets, Inc.
20141547: Glorianne Demoulas; Demoulas Super Markets, Inc.
20141552: Berkshire Fund VIII, L.P.; Access Information Holdings, LLC
20141556: 3i Group plc; Audax Private Equity Fund II, L.P.
20141562: Concordia Healthcare Corp.; Eisai Co., Ltd.
20141563: Hicks, Muse, Tate & Furst Equity Fund III, L.P.; Mercury New Holdco Inc.
20141564: Hicks, Muse, Tate & Furst Equity Fund IV, L.P.; Mercury New Holdco Inc.
Akorn, Inc., In the Matter of
Akorn, Inc. has agreed to sell its rights to develop, manufacture, and market the generic injectable tuberculosis drug, rifampin, in order to settle FTC charges that Akorn’s proposed acquisition of VersaPharm Inc. and its parent company, VPI Holdings Corp., would likely be anticompetitive. According to the FTC’s complaint, only VersaPharm and two other firms currently have FDA approval to sell generic injectable rifampin and there are no viable substitutes for rifampin as a course of treatment for tuberculosis. The FTC’s proposed settlement with Akorn requires the company to divest its Abbreviated New Drug Application for generic injectable rifampin – which is currently pending before the Food and Drug Administration – to Watson Laboratories, Inc.