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Lupin Ltd., et al., In the Matter of
Generic drug manufacturers Lupin Ltd. and Gavis Pharmaceuticals LLC agreed to sell the rights and assets for two generic drugs, in order to settle FTC charges that Lupin’s proposed $850 million acquisition of Gavis would likely be anticompetitive.The merger would have combined two of only four companies that currently market generic doxycycline monohydrate capsules in two dosage strengths, used to treat bacterial infections, likely resulting in higher prices. The merger also would have eliminated one of only a few companies likely to enter the market for generic mesalamine extended release capsules, used to treat ulcerative colitis, in the near future, thereby delaying beneficial competition and the prospect of price decreases. Under the terms of the order, Lupin is required to transfer to G&W Laboratories all of Gavis’s rights and assets related to generic doxycycline monohydrate capsules no later than ten days after the acquisition is consummated. The order also requires that Gavis divest its rights and assets related to generic mesalamine capsules to G&W before the acquisition takes place.
Star Pipe Products, Ltd. Agrees to $120,000 Civil Penalty and New Obligations to Settle Charges that It Violated FTC Order
FTC Chairwoman Edith Ramirez to Participate in International Competition Network Conference in Singapore
1604008 Informal Interpretation
Dollars, Doctrine, and Damage Control: How Disgorgement Affects the FTC’s Antitrust Mission
1604007 Informal Interpretation
1604005 Informal Interpretation
FTC and Justice Department Officials Meet with Officials of Chinese Antitrust Agencies
1604006 Informal Interpretation
1604004 Informal Interpretation
1604003 Informal Interpretation
FTC, DOJ Issue Joint Statement on Preserving Competition in the Defense Industry
FTC Workshop Will Examine Competition and Consumer Protection Issues in the Rooftop Solar Business
1604002 Informal Interpretation
Endo Pharmaceuticals / Impax Labs
The FTC filed a complaint in federal district court alleging that Endo Pharmaceuticals Inc. and several other drug companies violated antitrust laws by using pay-for-delay settlements to block consumers’ access to lower-cost generic versions of Opana ER and Lidoderm with an agreement not to market an authorized generic – often called a “no-AG commitment” – as a form of reverse payment. The complaint, filed in the Eastern District of Pennsylvania, alleges that Endo paid the first generic companies that filed for FDA approval – Impax Laboratories, Inc. and Watson Laboratories, Inc. – to eliminate the risk of competition for Opana ER and Lidoderm, in violation of the Federal Trade Commission Act. Opana ER is an extendedrelease opioid used to relieve moderate to severe pain. Lidoderm is a topical patch used to relieve pain associated with post-herpetic neuralgia, a complication of shingles. The FTC is seeking a court judgment declaring that the defendants’ conduct violates the antitrust laws, ordering the companies to disgorge their ill-gotten gains, and permanently barring them from engaging in similar anticompetitive behavior in the future. Teikoko Pharma USA and Teikoku Seiyaku Co., Ltd. agreed to a stipulated order resolving FTC charges.
In November 2016, the FTC voluntarily dismissed the complaint in this action. On January 23, 2017, the FTC refiled charges related to the Lidoderm agreements in federal court in California (Federal Trade Commission vs. Allergan plc; Watson Laboratories, Inc., et al) and refiled charges related to the Opana ER agreement in a Part 3 administrative proceeding. (In re Impax Laboratories, Inc.)
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