Connecticut v. Sandoz, Inc.

District Court, D. Connecticut·Decided July 21, 2025·No. 3:20-cv-00802·Unknown

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF CONNECTICUT

THE STATE OF CONNECTICUT; THE STATE OF ALASKA; THE STATE OF ARIZONA; THE STATE OF ARKANSAS; THE STATE OF No. 3:20-cv-00802-MPS CALIFORNIA; THE STATE OF COLORADO; THE STATE OF DELAWARE; THE DISTRICT OF

COLUMBIA; THE STATE OF FLORIDA; THE STATE OF GEORGIA; THE TERRITORY OF GUAM; THE STATE OF HAWAII; THE STATE OF IDAHO; THE STATE OF ILLINOIS; THE STATE OF INDIANA; THE STATE OF IOWA; THE STATE OF KANSAS; THE COMMONWEALTH OF KENTUCKY; THE STATE OF LOUISIANA; THE STATE OF MAINE; THE STATE OF MARYLAND; THE COMMONWEALTH OF MASSACHUSETTS; THE STATE OF MICHIGAN; THE STATE OF MINNESOTA; THE STATE OF MISSISSIPPI; THE STATE OF MONTANA; THE STATE OF NEBRASKA; THE STATE OF NEVADA; THE STATE OF NEW HAMPSHIRE; THE STATE OF NEW JERSEY; THE STATE OF NEW MEXICO; THE STATE OF NEW YORK; THE STATE OF NORTH CAROLINA; THE STATE OF NORTH DAKOTA; THE COMMONWEALTH OF THE NORTHERN MARIANA ISLAND; THE STATE OF OHIO; THE STATE OF OKLAHOMA; THE STATE OF OREGON; THE COMMONWEALTH OF PENNSYLVANIA; THE COMMONWEALTH OF PUERTO RICO; THE STATE OF RHODE ISLAND; THE STATE OF SOUTH CAROLINA; THE STATE OF TENNESSEE; THE STATE OF UTAH; THE STATE OF VERMONT; THE COMMONWEALTH OF VIRGINIA; THE STATE OF WASHINGTON; THE STATE OF WEST VIRGINIA; THE STATE OF WISCONSIN; and U.S. VIRGIN ISLANDS, Plaintiffs, v. SANDOZ, INC.; ACTAVIS HOLDCO US, INC.; ACTAVIS ELIZABETH LLC; ACTAVIS PHARMA, INC.; AMNEAL PHARMACEUTICALS, INC.; AMNEAL PHARMACEUTICALS, LLC; ARA APRAHAMIAN; AUROBINDO PHARMA U.S.A., INC.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH US, LLC; MITCHELL BLASHINSKY; DOUGLAS BOOTHE; FOUGERA PHARMACEUTICALS INC.; GLENMARK PHARMACEUTICALS INC., USA; JAMES (JIM) GRAUSO; GREENSTONE LLC; G&W LABORATORIES, INC.; WALTER KACZMAREK; ARMANDO KELLUM; LANNETT COMPANY, INC.; LUPIN PHARMACEUTICALS, INC.; MALLINCKRODT INC.; MALLINCKRODT LLC; MALLINCKRODT plc; MYLAN INC.; MYLAN PHARMACEUTICALS INC.; KURT ORLOFSKI; MICHAEL PERFETTO; PERRIGO NEW YORK, INC.; PFIZER INC.; SUN PHARMACEUTICAL INDUSTRIES, INC.; TARO PHARMACEUTICALS USA, INC.; TELIGENT, INC.; ERIKA VOGEL-BAYLOR; JOHN WESOLOWSKI; and WOCKHARDT USA LLC,

Defendants. RULING ON MOTION FOR SUMMARY JUDGMENT The plaintiffs, the Attorneys General of most of the States and several U.S. territories (“the States”), have moved under Federal Rule of Civil Procedure 56 for partial summary judgment as to liability related to four claims asserted against three of the thirty-six defendants in this sprawling action alleging price-fixing, market allocation, and bid rigging in the sale of generic drugs for skin ailments. The motion seeks summary judgment only on a single element—referred to as the violation or liability element, or “per se liability”—of antitrust claims against Sandoz Inc. (“Sandoz”), Taro Pharmaceuticals USA, Inc. (“Taro”), and Hector Armando Kellum (collectively, “Defendants”), related to a limited number of generic drugs during limited periods of time. For the reasons set forth below, I grant the States’ motion. I. FACTUAL AND PROCEDURAL BACKGROUND A. Procedural Background This is one of three cases in which the Attorneys General of the States and territories have sued scores of defendants in the generic drug industry for alleged antitrust violations and unfair

trade practices. All three cases were originally filed in this Court but were transferred to the Eastern District of Pennsylvania (the “MDL Court”), which was designated by the Judicial Panel on Multi-district Litigation (the “JPMDL) to preside over these and other cases brought by private parties involving similar allegations in a consolidated proceeding. ECF No. 9.1 In April 2024, these three cases were remanded to this Court by the JPMDL and assigned to me. ECF No. 11. The operative complaint in this case, the September 9, 2021 Amended Complaint (ECF No. 196 on this Court’s docket), spans 609 pages and includes 2,123 numbered paragraphs. It alleges collusion in the pricing, market allocation, and bidding for generic drugs for dermatological applications. (The parties refer to it as the “the Dermatology Complaint.”) Its allegations have been summarized in various rulings by the MDL Court, see, e.g., In re Generic Pharms. Pricing

Antitrust Litig., 338 F.Supp.3d 404, 411–34. (E.D. Pa. 2018); In re Generic Pharms. Pricing Antitrust Litig., 394 F. Supp. 3d 509, 514–24 (2019); and I adopt those summaries by reference. Essentially, the complaint describes a series of conspiracies, and an overarching conspiracy, between makers of generic dermatological drugs to collude on price and market allocation and to rig bids for the business of customers. This motion seeks summary judgment on one element of the antitrust claims under Count

1 Unless otherwise indicated, all ECF numbers in this case refer to entries on the docket of this case, not the same case when it was before the MDL Court, and each page number refers to the page number shown on the ECF stamp on the top of the cited page, not the page of the relevant brief or pleading designated by the parties. One (against Sandoz), Count Two (against Taro), Count Twenty-Three (against Kellum), and Twenty-Eight (state-law claims against Sandoz, Taro, and Kellum) of the Amended Complaint. Although the Amended Complaint alleges conspiracies related to the markets of eighty generic drugs, the motion seeks partial summary judgment only as to conspiracies on three: clobetasol (in

its cream, emollient cream, gel, ointment, and solution formulations) (“clobetasol”), desonide ointment, and nystatin triamcinolone cream. The States allege that clobetasol is a corticosteroid used to treat eczema, contact dermatitis, seborrheic dermatitis, and psoriasis; that desonide ointment is a topical steroid used to treat eczema, dermatitis, allergies, and rash; and that nystatin triamcinolone cream is used to treat cutaneous candidiasis, such as yeast infections and thrush. ECF No. 196 ¶¶ 655, 833, 869. Specifically, the States argue that there is no genuine issue of material fact to as to whether Sandoz and Taro conspired from March 2013 until December 2015 to fix prices and allocate customers for clobetasol, desonide ointment, and nystatin triamcinolone cream.2 The States also argue that there is no genuine issue of material fact as to whether Kellum (a former Sandoz

employee) conspired from March 2013 to June 2015 to fix prices and allocate customers for clobetasol and nystatin triamcinolone cream. B. Admissions The States’ motion rests entirely on whether the Defendants have each admitted to the conspiracies, either through (1) Sandoz and Taro’s deferred prosecution agreements (“DPA” or DPAs”) and Kellum’s plea agreement in the face of federal criminal charges; or (2) through the

2 It is undisputed that Sandoz and Taro were competitors in the manufacturing, marketing, and sale of certain generic drugs from March 2013 until December 2015, and that each sold clobetasol, desonide ointment, and nystatin triamcinolone cream. ECF Nos 555-1 ¶ 6–7 and 559-1 ¶ 6–7. Defendants’ Rule 36 responses to Requests for Admission, which adopted language from the criminal agreements. 1. Sandoz and Taro In 2020, Sandoz and Taro both entered into DPAs with the United States Department of

Justice (“DOJ”). ECF Nos. 555-1 at 17, 559-1 at 16. In these agreements, Sandoz and Taro each accepted responsibility for the conduct described in a criminal information the DOJ had filed against it and admitted to facts in an accompanying Statement of Facts. Id. Sandoz and Taro also each agreed not to make any public statement “in litigation or otherwise” that contradicted the acceptance of responsibility or any of the facts for a term of three years. Id.

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