Galderma Laboratories Inc. v. Amneal Pharmaceuticals, LLC

921 F. Supp. 2d 278, 2012 WL 3890942, 2012 U.S. Dist. LEXIS 127463
CourtDistrict Court, D. Delaware
DecidedSeptember 7, 2012
DocketC.A. No. 11-1106-LPS
StatusPublished
Cited by4 cases

This text of 921 F. Supp. 2d 278 (Galderma Laboratories Inc. v. Amneal Pharmaceuticals, LLC) 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
Galderma Laboratories Inc. v. Amneal Pharmaceuticals, LLC, 921 F. Supp. 2d 278, 2012 WL 3890942, 2012 U.S. Dist. LEXIS 127463 (D. Del. 2012).

Opinion

MEMORANDUM ORDER

LEONARD P. STARK, District Judge.

At Wilmington this 7th day of September, 2012:

IT IS HEREBY ORDERED that Defendants’ motion for partial judgment on the pleadings based on collateral estoppel (D.I. 52) (hereinafter, “Motion” or “Mot.”) is GRANTED for the following reasons:

In this Abbreviated New Drug Application (“ANDA”) patent litigation, Defendants, Amneal Pharmaceuticals, LLC and Amneal Pharmaceuticals Co. (I) Pvt. Ltd. (collectively, “Amneal”), move for judgment on the pleadings that their proposed 40 mg doxycycline product does not infringe the “Ashley patents.” 1 Amneal’s Motion is based on collateral estoppel (issue preclusion). Specifically, Amneal relies on this Court’s-finding in a related ANDA action2 (hereinafter, “the Mylan Action”) that a proposed generic product [280]*280containing 40 mg doxycycline administered once daily does not infringe the Ashley patents, because such products do not contain the required “sub-antibacterial amounts” of doxycycline but, rather, significantly inhibit the growth of microorganisms. See Mylan, 809 F.Supp.2d at 317 & n. 12.

Plaintiffs, Galderma Laboratories Inc., Galderma Laboratories, L.P., and Super-nus Pharmaceuticals, Inc. (collectively, “Galderma”), who assert the Ashley patents against Amneal, oppose the Motion. (D.I. 59) Galderma contends that collateral estoppel does not apply because the instant action does not present the “identical issue!” as the Mylan Action. In Galderma’s view, the Motion must be denied because this case involves Amneal’s proposed product, while the Mylan Action involved Mylan’s different proposed product. Galderma also insists that the Motion is premature because Galderma has not yet taken discovery on Amneal’s proposed product. Galderma further asserts that granting the Motion will undermine judicial efficiency, given the potential outcome of its pending appeal in the Mylan Action.

Pursuant to Federal Rule of Civil Procedure 12(c), a party may move for judgment on the pleadings,. “[ajfter pleadings are closed' — -but early enough not to delay trial.” As the Third Circuit has explained, in authority on which Galderma relies (D.I. 59 at 3):

“Under Rule 12(c), judgment will not be granted unless the movant clearly establishes that no material issue of fact remains to be resolved and that he is entitled to judgment as a matter of law. In reviewing the grant of a Rule 12(c) motion, we must view the facts presented in the pleadings and the inferences to be drawn therefrom in the light most favorable to the nonmoving party.”

Domino’s Pizza LLC v. Deak, 383 Fed.Appx. 155, 158 (3d Cir.2010) (quoting Rosenau v. Unifund Corp., 539 F.3d 218, 221 (3d Cir.2008)). “[Jjudgment will not be granted unless the movant clearly establishes there are no material issues of fact, and he is entitled to judgment as a matter of law.” Sikirica v. Nationwide Ins. Co., 416 F.3d 214, 220 (3d Cir.2005). A Rule 12(c) motion is subject to the same standard as a Rule 12(b)(6) motion to dismiss. See Citisteel USA Inc. v. Gen. Elec. Co., 78 Fed.Appx. 832, 835 n. 3 (3d Cir.2003).

A party asserting collateral estoppel must prove the following elements: (1) the previous determination was necessary to the decision; (2) the identical issue was previously litigated; (3) the issue was actually decided on the merits and the decision was final and valid; and (4) the party being precluded from re-litigating the issue was adequately represented in the previous action. See Jean Alexander Cosmetics, Inc. v. L’Oreal USA, Inc., 458 F.3d 244, 249 (3d Cir.2006); Novartis Pharms. Corp. v. Abbott Labs., 375 F.3d 1328, 1333 (Fed.Cir.2004).

Galderma essentially concedes all but the second of the four elements of collateral estoppel. With respect to element (1), Galderma, in its opposition, does not contest (and, of course, it cannot) that the Court’s finding of non-infringement of the Ashley patents was necessary to the Court’s decision in the Mylan Action, given that Galderma asserted there that Mylan infringed the Ashley patents. With respect to element (3), Galderma does not challenge Amneal’s contention that the issue of infringement of the Ashley patents was actually decided in the Mylan Action, and that decision (although currently on appeal) is presently embodied in a final and valid judgment. With respect to element (4), Galderma concedes by its silence that it was adequately represented in the [281]*281Mylan Action (in which, not incidentally, it was represented by the same able counsel as represents it in the instant action), an action in which it had a full and fair opportunity — culminating in a four-day bench trial followed by substantial post-trial briefing — to litigate infringement of the Ashley patents.3

The dispute, then, is whether Galderma’s claim that Amneal infringes the Ashley patents presents the “identical issue” that was previously litigated and decided against Galderma in the Mylan Action. On this question, the Court agrees with Amneal.

In the Mylan Action, the Court decided whether a product containing 40 mg of doxycycline, administered once daily, infringes the Ashley patents. See Mylan, 809 F.Supp.2d at 317-22. It is undisputed that Amneal’s ANDA, like Mylan’s ANDA, seeks FDA approval to market a product containing 40 mg of doxycycline to be administered once daily. (D.I. 1 ¶ 27) Hence, in order to prevail against Amneal on its claim for infringement of the Ashley patents, Galderma would have to prevail on the “identical issue” it previously litigated — and lost — in the Mylan Action.

In response to this simple logic, Galderma argues that no identical issue is presented here, because the Mylan Action involved Mylan’s proposed product while the instant action involves Amneal’s different proposed product. Galderma even suggests that Amneal has somehow been inconsistent, claiming that Amneal has, over the course of this litigation, argued “that its generic product has a distinct formulation from Mylan’s generic product.” (D.I. 59 at 2) Galderma’s argument lacks merit. Galderma identifies no actual inconsistency in Amneal’s position. Instead, the two citations on which Galderma relies — a portion of Amneal’s brief opposing Galderma’s motion to stay (which the Court denied, see D-I. 56), and a statement Amneal made during a scheduling conference (see D.I. 59 at 4, 6) (citing D.I. 21 at 10; D.I. 34 at 10) — show that Amneal has consistently argued its proposed product differs from Mylan’s proposed product in terms of their overall formulations, a matter having nothing to do with the Ashley patents.4

Galderma’s remaining arguments are likewise flawed. Galderma places heavy emphasis on the fact that its appeal of the Court’s ruling in the Mylan Action is pending, presenting the possibility that the Federal Circuit will reverse or vacate the Court’s finding of non-infringement on the Ashley patents.

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921 F. Supp. 2d 278, 2012 WL 3890942, 2012 U.S. Dist. LEXIS 127463, Counsel Stack Legal Research, https://law.counselstack.com/opinion/galderma-laboratories-inc-v-amneal-pharmaceuticals-llc-ded-2012.