Hartig Drug Co. v. Senju Pharmaceutical Co.

122 F. Supp. 3d 202, 2015 U.S. Dist. LEXIS 109367, 2015 WL 4935500
CourtDistrict Court, D. Delaware
DecidedAugust 19, 2015
DocketCiv. No. 14-719-SLR
StatusPublished

This text of 122 F. Supp. 3d 202 (Hartig Drug Co. v. Senju Pharmaceutical Co.) is published on Counsel Stack Legal Research, covering District Court, D. Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hartig Drug Co. v. Senju Pharmaceutical Co., 122 F. Supp. 3d 202, 2015 U.S. Dist. LEXIS 109367, 2015 WL 4935500 (D. Del. 2015).

Opinion

MEMORANDUM OPINION

ROBINSON, District Judge

I. INTRODUCTION

On June 6, 2014, plaintiff Hartig Drug Company, Inc. (“Hartig” or “plaintiff’) filed a complaint alleging certain antitrust violations concerning defendants Senju Pharmaceutical Co., Ltd. (“Senju”), Kyorin Pharmaceutical Cp., Ltd. (“Kyorin”), and Allergan,: Inc.’s (“Allergan”) (collectively “defendants”) aqueous liquid gatifloxacin ophthalmic products, Zymar® and Zymax-id®. (D.I. 1) Defendants are the owners or licensees of U.S. Patent Nos. ■ 4,980,470 (“the ’470 patent”) and 5,880,283 (“the ’283 patent”), which are listed in the United States Food and Drug Administration’s (“FDA’s”) publication titled “Approved Drug Products with Therapeutic Equivalence Evaluations” (known as the “Orange Book”) for Zymar® and Zymaxid®.-(Id. at ¶¶ 36, 42, 45, 51, 72-73) Hartig brings this putative class action on behalf of all direct purchasers in the. United States who purchased or paid for branded. Zymar® or Zymaxid® products from June 15, 2010 until the allegedly anticompetitive effects of defendants’ conduct cease (the “class period”). (Id. at ¶ 1) Hartig purchased Zy-mar® and Zymaxid® from Amerisource-Bergen Drug Corporation (“Ameri-Source”). (Id. at ¶ 9) AmeriSource directly purchased Zymar® and Zymaxid® from Allergan subject to ’ a distribution services agreement (”DSA‘) during the class period. (Id.)

Hartig asserts that defendants engaged in unlawful anticompetitive acts and practices including:1 (1) filing sham patent lawsuits; (2) committing fraud upon the United States Patent & . Trademark Office (“USPTO”); and (3) “product hopping” to preclude pharmacies from substituting generic gatifloxacin ophthalmic formulations form defendants’ more expensive branded drugs. (Id. at ¶ 3) Specifically, Hartig alleges that defendants: (1) monopolized in violation of Section 2 of the Sherman Act; (2) conspired to monopolize in violation of Section 2 of the Sherman Act; and (3) contracted, combined, or conspired to restrain trade in violation of Section -1 of the Sherman Act. (Id. at ¶¶ 153-192) Presently before the court- is Allergan’s motion to dismiss under Fed. R. Civ.- P. 12(b)(1) for lack of jurisdiction over the subject matter (D.I. 14), and Kyorin and Senju’s joint motion to dismiss under Fed. R. Civ. P. [205]*20512(b)(6) for failure to state a claim (D.I. 17).2 The court has jurisdiction pursuant to U.S.C. §§ 1331 and 1337(a) and 15 U.S.C. § 15.

II. STANDARD OF REVIEW

Not only may the lack of subject matter jurisdiction be raised at any time, it cannot be waived and the court is obliged to address the issue on its own motion. See Moodie v. Fed. Reserve Bank of NY, 58 F.3d 879, 882 (2d Cir.1995). Once jurisdiction is challenged, the party asserting subject matter jurisdiction has the burden of proving its existence. See Carpet Group Int’l v. Oriental Rug Importers Ass’n, Inc., 227 F.3d 62, 69 (3d Cir.2000). Under Rule 12(b)(1), the court’s jurisdiction may be challenged either facially (based on the legal sufficiency of the claim) or factually (based on the sufficiency of jurisdictional fact). See 2 James W. Moore, Moore’s Federal Practice § 12.30[4] (3d ed. 1997). Under a facial challenge to jurisdiction, the court must accept as true the allegations contained in the complaint. See id. Dismissal for a facial challenge to jurisdiction is “proper only when the claim ‘clearly appears to be immaterial and made solely for the purpose of obtaining jurisdiction or ... is wholly insubstantial and frivolous.’ ” Kehr Packages, Inc. v. Fidelcor, Inc., 926 F.2d 1406, 1408-09 (3d Cir.1991) (quoting Bell v. Hood, 327 U.S. 678, 682, 66 S.Ct. 773, 90 L.Ed. 939 (1946)).

Under a factual attack, however, the court is not “eonfine[d] to allegations in the ... complaint, but [can] consider affidavits, depositions, and testimony to resolve factual issues bearing on jurisdiction.” Gotha v. United States, 115 F.3d 176, 179 (3d Cir.1997); see also Mortensen v. First Fed. Sav. & Loan Ass’n, 549 F.2d 884, 891-92 (3d Cir.1977). In such a situation, “no presumptive truthfulness attaches to plaintiffs allegations, and the existence of disputed material facts will not preclude the trial court from evaluating for itself the merits of jurisdictional claims.”- Carpet Group, 227 F.3d at 69 (quoting Mortensen, 549 F.2d at 891).

III. DISCUSSION

Section 4 of Clayton Act provides a private cause of action for “any person injured in his business or property by reason of anything forbidden in the antitrust laws.” 15 U.S.C. § 15. In Illinois Brick Co. v. Illinois, 431 U.S. 720, 735, 97 S.Ct. 2061, 52 L.Ed.2d 707 (1977), the United States Supreme Court “established the general rule that only direct purchasers from antitrust violators may recover damages in antitrust suits.”" Howard Hess Dental Labs. Inc. v. Dentsply Int’l, Inc., 424 F.3d 363, 369 (3d Cir.2005). Indirect purchasers are generally not entitled to recover damages for passed-on overcharges. Id. This is referred to as the “indirect purchaser rule.” Three policy reasons justified the Court’s decision to impose this rule: “(1) a risk of duplicative liability for defendants and potentially inconsistent adjudications could arise if courts permitted both direct and indirect purchasers to sue defendants for the same overcharge; (2) the evidentia-ry complexities and uncertainties involved in ascertaining the portion of the overcharge that the direct purchasers had passed on to the various levels of indirect purchasers would place too great a burden on the courts; and. (3) permitting direct and indirect purchasers to sue only for the amount of the overcharge they themselves absorbed and did not pass on would cause inefficient enforcement of the antitrust laws by diluting the ultimate recovery and thus decreasing the direct 'purchasers’ incentive to sue.” Id. at 369-70.

[206]*206Hartig does not allege that it purchased Zymar® and Zymaxid® directly from defendants during the class period. (D.I. 1 at ¶ 9) Rather, Hartig contends that it has standing to sue as a direct purchaser in that AmeriSource “conveyed, assigned, and transferred to Hartig all of its rights, title and interest in and to all causes of action it may have against Defendants under the antitrust laws of the United States ... arising out of or relating to Ameri-source’s purchase of Zymar and Zymaxid.” (D.I. 1 at ¶ 9) Allergan does not dispute that “an antitrust claim can be expressly assigned.” Gulfstream III Associates, Inc. v. Gulfstream Aerospace Corp.,

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Bell v. Hood
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Blue Shield of Va. v. McCready
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Sheila Gotha v. United States
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Mortensen v. First Federal Savings & Loan Ass'n
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Kehr Packages, Inc. v. Fidelcor, Inc.
926 F.2d 1406 (Third Circuit, 1991)

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Bluebook (online)
122 F. Supp. 3d 202, 2015 U.S. Dist. LEXIS 109367, 2015 WL 4935500, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hartig-drug-co-v-senju-pharmaceutical-co-ded-2015.