The legal library gives you easy access to the FTC’s case information and other official legal, policy, and guidance documents.
1809005 Informal Interpretation
20182067: SS&C Technologies Holdings, Inc.; Impala Private Investments, LLC
Pharmavite, LLC (NatureMade Omega-3 with Xtra Absorb Technology Supplements)
Mikey & Momo, Inc. (Aromaflage), In the Matter of
Statement of Commissioner Rohit Chopra In the Matter of Aromaflage
Donor Relations LLC & Courtesy Call, Inc.
Tatto, Inc., also d/b/a Winbigbidlow and Tatto Media, et al.
Statement of Commissioner Chopra on the Departure of Maureen Ohlhausen
20181756: H.I.G. Advantage Buyout Fund, L.P.; Audax Private Equity Fund III, L.P.
Test Procedures and Labeling Standards for Recycled Oil
16 CFR Part 311: Test Procedures and Labeling Standards for Recycled Oil; Incorporation by Reference of Updated Publication
Vantage Point Services, LLC, et al.
20182035: Kayne Private Energy Income Fund II, L.P.; Southwestern Energy Company
Shire ViroPharma
The FTC filed a complaint in federal district court charging Shire ViroPharma Inc. with violating the antitrust laws by abusing government processes to delay generic competition to its branded prescription drug, Vancocin HCl Capsules. The complaint alleges that to maintain its monopoly, ViroPharma waged a campaign of serial, repetitive, and unsupported filings with the U.S. Food and Drug Administration and courts to delay the FDA’s approval of generic Vancocin Capsules, and exclude competition. According to the FTC, ViroPharma submitted 43 filings with the FDA and filed three lawsuits against the FDA between 2006 and 2012. According to the FTC, ViroPharma knew that it was the FDA’s practice to refrain from approving any generic applications until it resolved any pending relevant citizen petition filings. Viropharma intended for its serial filings to delay the approval of generics, and thus competition and lower prices. The FTC seeks a court order permanently prohibiting ViroPharma from submitting repetitive and baseless filings with the FDA and the courts, and from similar and related conduct as well as any other necessary equitable relief, including restitution and disgorgement.