In re Propranolol Antitrust Litigation

249 F. Supp. 3d 712, 2017 WL 1287515, 2017 U.S. Dist. LEXIS 53390
CourtDistrict Court, S.D. New York
DecidedApril 6, 2017
Docket16-CV-09901 (JSR)
StatusPublished
Cited by25 cases

This text of 249 F. Supp. 3d 712 (In re Propranolol Antitrust Litigation) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Propranolol Antitrust Litigation, 249 F. Supp. 3d 712, 2017 WL 1287515, 2017 U.S. Dist. LEXIS 53390 (S.D.N.Y. 2017).

Opinion

[715]*715OPINION AND ORDER

JED S. RAKOFF, United States District Judge

Plaintiffs FKW Holdings and' Cesar Castillo (the “Direct Purchasers”) and Sergeants Benevolent Association Health & Welfare Fund and American Federation of State, County and Municipal Employees District Council 37 Health & Security Plan (the “End-Payors”) bring putative nationwide class actions alleging that defendants illegally conspired to fix the price of the generic drug, propranolol hydrochloride (“Propranolol”). By Bottom-Line Order dated February 27, 2017 (the “Bottom-Line Order”), the Court denied the motion by defendants Heritage Pharmaceuticals Inc. (“Heritage”) and Upsher-Smith Laboratories, Inc. (“Upsher-Smith”) to dismiss the Direct Purchasers’ original complaints for lack of personal jurisdiction. See ECF No. 108, Defendants now jointly move to dismiss the Direct Purchasers’ and End-Payors’ consolidated amended complaints. For the reasons set forth below, this Opinion and Order denies defendants’ instant motions, except for part of their motion to dismiss certain state law claims in the End-Payors’ action. This Opinion and Order also explains the reasoning for the previous Bottom-Line Order,

On a motion to dismiss, the Court accepts all well-pleaded factual allegations as true and draws all reasonable inferences in favor of the non-moving party. See Goldstein v. Pataki, 516 F.3d 50, 56 (2d Cir. 2008). In the antitrust - context, stating a claim' under Section 1 of the Sherman Act “requires a complaint with enough factual matter (taken as true) to suggest that an agreement was made. Asking for plausible grounds to infer an agreement does not impose a probability requirement at the pleading stage; it simply calls for enough fact to raise a reasonable expectation that discovery will reveal evidence of illegal agreement.” Bell Atl. Corp. v. Twombly, 550 U.S. 544, 556, 127 S.Ct. 1955, 167 L.Ed.2d 929 (2007).

Propranolol is the generic version of In-deral and comes in two forms: capsules and tablets. Direct Purchasers’ Consolidated Amended Complaint (“DPP”) ¶¶ 81-83, ECF No. 109; End-Payors’ Consolidated Amended Complaint (“EPP”) ¶¶ 1-2, 46-51, Dkt. No. 17-cv-01039, ECF No. 60. The pleadings allege two conspiracies, with one overlapping defendant, to manipulate the price of both forms of the drug. DPP ¶¶ 8-9; EPP ¶¶ 1-2, 46-51. The defendants in the “Capsules Conspiracy” are Actaris Elizabeth, LLC (“Aetaris”), Breckenridge Pharmaceuticals, Inc. (“Breeken-ridge”), and Upsher-Smith (collectively, the “Capsules Defendants”). DPP ¶¶ 46-62; EPP ¶¶ 19-31. The defendants in the “Tablets Conspiracy” are Mylan Inc., Mylan Pharmaceuticals Inc., and UDL Laboratories, Inc. (collectively, “Mylan”), Teva Pharmaceuticals USA, Inc., and Pliva, Inc. (collectively, “Teva”), Endo International PLC, Par Pharmaceuticals Holdings, Inc., and Qualitest Pharmaceuticals, Inc. (collectively, “Par”), Heritage, and Actaris (collectively, the “Tablets Defendants”). Id.

The well-pleaded allegations of the complaints here at issue show the following facts:.

[716]*716Prior to 2013, the price of Propranolol had steadily declined since it entered the market in 1967. DPP ¶ 82; EPP ¶ 40; see DPP ¶¶ 78-79; EPP ¶67. This was not unusual in the case of generic drugs. In particular, because federal law requires each generic to be “readily substitutable for another generic of the same brand drug, the products behave like commodities, with pricing being the main differentiating feature and the basis for competition among manufacturers.” Id. As a result, prices in a “mature generic market, such as the market for [P]ropranolol” will fall until they stabilize at the generic manufacturers’ marginal costs of production. DPP ¶ 82; EPP ¶ 40.

Accordingly to the complaints, the prices of various dosages of Propranolol capsules had either consistently declined or somewhat stabilized prior to the Capsules Conspiracy. DPP ¶¶ 154; EPP ¶¶ 48-52. In either March or November of 2013,1 however, the Capsules Defendants abruptly began increasing their effective prices by significant amounts, DPP ¶¶ 114, 124, 126; EPP ¶¶ 2, 42, and continued to raise prices until approximately May 2014. EPP ¶¶ 153-173. Prices then remained relatively stable for a period of months until slightly falling to amounts still above pre-conspiracy levels. Id.

Several months later, a similar occurrence developed with regard to Proprano-lol tablets. After years of stable or declining prices, the Tablet Defendants abruptly raised the effective price of all dosages of Propranolol tablets in early 2015. Defendant Heritage increased effective prices by 102%-151% in January 2015, and, a few weeks later, defendants Teva and Actavis increased their own prices in March 2015 by 566%-898% and 395%-638%, respectively, DPP ¶ 186; EPP ¶¶ 49-52. Defendants Mylan and Par began increasing their prices soon after, in April and June, by amounts ranging from 55% to 607% and 52% to 216%, respectively. DPP ¶¶ 193-194, 199-201; EPP ¶¶49-52.2 Defendants’ prices continued to increase over the next year by as much as 1, 736%. DPP ¶¶ 136-213; EPP ¶¶ 49-52; see DPP ¶202 (“Between December 2014 and November 2015, Actavis raised the price of 80mg proprano-lol tablets by 1,736% (from $0.03 per tablet to $0.46 per tablet).”).

Economic factors make the Propranolol market susceptible to collusion, including industry concentration, barriers to entry, lack of substitutes, demand inelasticity, and interchangeability. See DPP ¶¶225-245; EPP ¶¶ 53-68. In addition, during the period of these price increases, there was no significant increase in production costs, no significant decrease in supply, and no significant increase in demand. DPP ¶¶ 214, 254-255; EPP ¶43. Federal law [717]*717further requires drug manufacturers to report potential drug shortages to the Food and Drug Administration (“FDA”), and no supply disruption was reported during the duration of the alleged conspiracies. DPP ¶¶ 222-224.3

Finally, state and federal agencies are conducting large-scale investigations of the generic drug industry for alleged price fixing. DPP ¶¶ 10-23, 38-45, 92-94, 241; EPP ¶¶ 5-6, 103, 108. Defendant Mylan disclosed in October 2016 that it had received a subpoena from the Department of Justice (“DOJ”) seeking information relating to the “marketing, pricing and sale” of several generic drugs, “including Propra-nolol.” DPP ¶ 43; EPP ¶ 103. Two months later, on December 14, 2016, the DOJ charged the former chief executive officer (“CEO”) and former president of defendant Heritage for criminal violations of the Sherman Act in connection with the generic drugs Glyburide and Doxycycline Hyc-late DR. DPP ¶¶ 15-16; EPP ¶ 5,104. The two individuals, Jason Málek and Jeffrey Glazer, subsequently plead guilty and are cooperating. Id.

Plaintiff FWK Holdings LLC filed suit against defendants on December 23, 2016 on behalf, of direct purchasers of Proprano-lol for violations of § 1 of the Sherman Act. Plaintiff Cesar Castillo Inc. filed a largely identical class action approximately two weeks later on January 5, 2017.

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249 F. Supp. 3d 712, 2017 WL 1287515, 2017 U.S. Dist. LEXIS 53390, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-propranolol-antitrust-litigation-nysd-2017.