In Re Terazosin Hydrochloride Antitrust Litigation

160 F. Supp. 2d 1365, 2001 WL 1002711
CourtDistrict Court, S.D. Florida
DecidedJuly 25, 2001
Docket99-MDL-1317
StatusPublished
Cited by28 cases

This text of 160 F. Supp. 2d 1365 (In Re Terazosin Hydrochloride Antitrust Litigation) is published on Counsel Stack Legal Research, covering District Court, S.D. Florida primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Terazosin Hydrochloride Antitrust Litigation, 160 F. Supp. 2d 1365, 2001 WL 1002711 (S.D. Fla. 2001).

Opinion

ORDER GRANTING DEFENDANTS’ MOTION TO DISMISS CERTAIN COUNTS OF THE INDIRECT PURCHASER PLAINTIFFS’ COMPLAINT

SEITZ, District Judge.

Defendants Abbott Laboratories [“Abbott”], Geneva Pharmaceuticals, Inc. [“Geneva”], and Zenith Goldline Pharmaceuticals, Inc. [“Zenith”] have moved to dismiss federal and state antitrust or unjust enrichment claims raised by “indirect purchasers” — individuals, corporations, and employee health plans that purchased prescription drugs containing terazosin hydrochloride after October 15, 1995, for consumption or redistribution' instead of resale. (Defs.’ Mot., Oct. 6, 2000 [D.E. No. 245].) Having carefully weighed the arguments presented by the parties, the Court will grant the defendants’ motion in part and allow the indirect purchaser *1368 plaintiffs, also known as “end payors,” to file a third amended class action complaint.

BACKGROUND

In Spring, 1998, Abbott entered into secret accords with generic drug makers Geneva and Zenith to forestall competition in its lucrative and exclusive domestic market for terazosin hydrochloride drugs. Abbott’s drug, “Hytrin,” was the only terazo-sin hydrochloride drug available in the United States for the treatment of hypertension or enlarged prostate until Geneva introduced its generic version of Hytrin on August 12, 1999. See In re Terazosin Hydrochloride Antitrust Litig., Civ. No. 99-MDL-1317, slip. op. at 8-11, — F.Supp.2d -, --- (S.D.Fla. Dec. 13, 2000) (recounting terms of agreements, which sought to preclude Geneva and Zenith from marketing the first generic tera-zosin hydrochloride drugs in the nation for some time, removed the risk that they would buy or sell the right to introduce such drugs in the interim, and enlisted them as allies who would oppose or at least ignore other companies’ applications to produce such drugs).

Both the end payors and the “direct purchasers,” who purchased terazosin hydrochloride drugs principally for resale, have filed class action complaints alleging that the defendants’' clandestine accords violated federal and state antitrust or consumer protection statutes. On December 13, 2000, this Court granted the direct purchasers’ motion for a partial summary judgment that these agreements were patently anti-competitive, unreasonable, and illegal per se under section one of the Sherman Antitrust Act, 15 U.S.C. § 1. Id. at 11-12, 18-19, -, -. Later in these proceedings, the direct purchasers will seek to prove that the defendants’ illegal conduct actually injured them in “business or property” under section four of the Clayton Act, 15 U.S.C. § 15.

DISCUSSION

The defendants’ motion to dismiss essentially asks whether the end payors are legally entitled to the benefit of the Court’s partial summary judgment decision in favor of the direct purchasers. As the defendants challenge the indirect purchasers’ right to sue under both federal and state laws, the Court will address the parties’ arguments in that order.

1. Standard Governing Dismissal for Failure to State a Claim

Federal Rule of Civil Procedure 12(b)(6) provides that dismissal of a claim is appropriate “only if it is clear that no relief could be granted under any set of facts that could be proved consistent with the allegations.” Blackston v. Alabama, 30 F.3d 117, 120 (11th Cir.1994) (citation omitted). The Court must accept the indirect purchasers’ allegations as true and view those allegations in a favorable light to determine whether the complaint fails to state a claim for relief. S & Davis Int’l, Inc. v. Republic of Yemen, 218 F.3d 1292, 1298 (11th Cir.2000).

2. The Indirect Purchasers’ Federal Claims and Illinois Brick

Three federal claims appear in the end payors’ second amended complaint [“complaint”]. Count One charges Abbott with “extending] its monopoly power beyond the lawful boundaries of its patents,” and Count Three charges all defendants with conspiring to “allow[ ] Abbott to maintain its monopoly,” both “in violation of [s]ection [two] of the Sherman Act, 15 U.S.C. § 2.” (Compl., Aug. 31, 2000, at 34, 39-40 [D.E. No. 227].) Count Five charges Abbott, Geneva, and Zenith with entering into contracts that were unreasonable restraints of trade under section one of the Sherman Act. (Id. at 42.) In all of these counts, the class plaintiffs allege *1369 that “their injury consists of paying more for terazosin [hydrochloride] than they would have paid in the absence of [the antitrust] violation.” (Id. at 34, 40, 42.)

Nearly twenty five years ago, in Illinois Brick Co. v. Illinois, 431 U.S. 720, 97 S.Ct. 2061, 52 L.Ed.2d 707 (1977), the United States Supreme Court held that indirect purchasers of goods produced by firms engaged in price-fixing or other antitrust violations cannot pursue federal antitrust actions for damages against those firms. Illinois Brick Co., 431 U.S. at 745-48, 97 S.Ct. 2061 (discussing section four of the Clayton Antitrust Act, 15 U.S.C. § 15(a)). Although this decision “denies recovery to those indirect purchasers who may have been actually injured by antitrust violations,” it simplifies private enforcement and public adjudication of antitrust suits by “elevating direct purchasers to a preferred position,” id. at 748, 97 S.Ct. 2061, and complements the U.S. Supreme Court’s decision in Hanover Shoe, Inc. v. United Shoe Machinery Corp., 392 U.S. 481, 88 S.Ct. 2224, 20 L.Ed.2d 1231 (1968), which precluded defendants from challenging federal antitrust claims with evidence that direct purchasers “passed on” an illegal overcharge to their own customers. Illinois Brick Co., 431 U.S. at 736-47, 97 S.Ct. 2061.

Illinois Brick blocks the end payors’ federal claims. Although the end payors contend that they have suffered a unique injury in the form of “lost savings,” (Pls.’ Opp’n, Nov. 3, 2000, at 3 [D.E. No. 274]), this locution does not disguise the fact that they are seeking damages for “paying more for terazosin [hydrochloride].” (Compl. at 34, 40, 42.) Like the direct purchasers, the end payors want to recoup an overcharge under federal law. The U.S. Supreme Court has flatly repudiated such efforts to trace damages through multiple levels in a chain of distribution or to apportion damages between direct and indirect purchasers. Illinois Brick Co., 431 U.S. at 746, 97 S.Ct. 2061.

Contrary to the plaintiffs’ suggestion, none of the exceptions to Illinois Brick apply here.

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Bluebook (online)
160 F. Supp. 2d 1365, 2001 WL 1002711, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-terazosin-hydrochloride-antitrust-litigation-flsd-2001.