AstraZeneca AB v. Dr. Reddy's Laboratories, Inc.

209 F. Supp. 3d 744, 2016 U.S. Dist. LEXIS 94440, 2016 WL 3946799
CourtDistrict Court, D. Delaware
DecidedJuly 20, 2016
DocketCiv. No. 15-988-SLR
StatusPublished
Cited by10 cases

This text of 209 F. Supp. 3d 744 (AstraZeneca AB v. Dr. Reddy's Laboratories, Inc.) 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
AstraZeneca AB v. Dr. Reddy's Laboratories, Inc., 209 F. Supp. 3d 744, 2016 U.S. Dist. LEXIS 94440, 2016 WL 3946799 (D. Del. 2016).

Opinion

MEMORANDUM OPINION

ROBINSON, District Judge

I. INTRODUCTION

On October 28, 2015, plaintiffs AstraZ-eneca AB, AstraZeneca LP, and AstraZ-eneca Pharmaceuticals LP (collectively, “plaintiffs”) filed this trademark suit against defendant Dr. Reddy’s Laboratories, Inc. (“defendant”) alleging, inter alia, trademark infringement and counterfeiting, for defendant’s use of the color purple on, and relating to the marketing of, its generic version of Nexium®. (D.I. 1) Presently before the court are defendant’s motion to transfer (D.I. 68) and motion for partial judgment on the pleadings (D.I. 66), as well as plaintiffs’ motion to dismiss [747]*747the counterclaim (D.I. 75). The court has jurisdiction pursuant to 15 U.S.C § 1121, and 28 U.S.C. §§ 1331, 1338 (a) and (b). The court has supplemental jurisdiction over the counterclaim pursuant to 28 U.S.C. § 1366.

II. BACKGROUND 1

A. Parties

Plaintiff AstraZeneca AB is a company operating and existing under the laws of Sweden with its principal place of business in Sodertalje, Sweden. Plaintiffs AstraZ-eneca LP and AstraZeneca Pharmaceuticals LOP are limited partnerships organized and existing under the laws of the State of Delaware with addresses in Wilmington, Delaware. Defendant Dr. Red-dy’s Laboratories, Inc. is a corporation organized and existing under the laws of the State of New Jersey with its principal place of business in Princeton, New Jersey. (D.I. 1 at ¶¶ 3-6) Plaintiffs and defendant, independently, conduct business in Delaware related to the issue at bar. (D.I. 1 at ¶ 8)

B. Factual Background

Since 1989, plaintiffs have used the color purple to brand their gastrointestinal (“GI”) products2 for treating severe heartburn and acid reflux. The U.S. Patent and Trademark Office has confirmed the brand status of plaintiffs’ purple color by awarding plaintiffs three federal trademark registrations covering the color purple for GI pharmaceuticals and one covering the phrase “THE PURPLE PILL®” for the same goods. (D.I. 5 at 10) Several companies have recently entered the market with generic versions of plaintiffs’ Nexium® esomeprazole magnesium compound. The first two companies permitted by the FDA to do so—Teva and Mylan—have used blue or white capsules. Defendant, a maker of generic drugs, launched its generic GI pharmaceutical (esomeprazole) in September 2015 and manufactured its generic version of Nexium® in two-tone purple pills.

C.Previous Litigation

In 2008, plaintiffs brought suit (the “2008 ANDA litigation”)3 against defendant in the District of New Jersey “over the sale of a generic version of ... Nexi-um®.” (D.I. 69 at 1) Defendant had filed an ANDA with the FDA for its generic version. (Id. at 2) Defendant allegedly provided the ANDA and samples to plaintiffs. (Id. at 3) In 2011, the parties executed a Settlement Agreement and the District of New Jersey entered a Consent Judgment. (Id. at 1) The Settlement Agreement and Consent Judgment (collectively, the “Agreement”) provided in Section 3.1:

In settlement of the disputed claims in the Action, and in consideration of the representations, warranties and covenants contained in this Settlement Agreement, subject to and effective only upon entry of the Consent Judgment (whether with or without modification as provided for in Section 2.2), AstraZeneca, on behalf of itself and its Affiliates, and its and their respective predecessors, successors, assigns, agents, officers, directors, employees and representatives, hereby fully, finally and irrevocably relinquishes, releases and discharges [Dr. Reddy’s
[748]*748Laboratories, Inc. (“DRL”) ] and its Affiliates, and its and their respective predecessors, successors, assigns, agents, officers, directors, employees, representatives, suppliers, importers, manufacturers, distributors and customers (the “DRL Releasees”), from any and all claims, demands, damages, liabilities, obligations, and causes of action known or unknown, suspected or unsuspected, in law or equity, including costs, expenses and attorneys’ fees, that were asserted, or that could have been asserted, by AstraZeneca or any of its Affiliates in connection with the DRL Product, the Approved Nexium Product or the Actions and arising before the Effective Date of this Settlement Agreement.

(D.I. 79 at 4) Section 6.2(a) similarly states plaintiffs will not sue defendant for “[flosses, known or unknown, suspected or unsuspected, in law or equity, that were asserted or that could have been asserted by AstraZeneca ... in connection with the [defendant’s product] or the Actions and arising before the Effective Date of this Settlement Agreement ....” (Id.) Section 6.2(c) prohibits plaintiffs from taking action “to prevent the launch, manufacture, use, sale, offer for sale, importation or distribution of [defendant’s] product ... as permitted under the terms of [the Agreement].” (Id. at 5) Section 9.13 addresses the trademark rights:'

Limitation of Rights Granted. Except for the rights, agreements and covenants specifically granted pursuant to this Settlement Agreement, no other rights, agreements or covenants are granted or implied by this Settlement Agreement. DRL shall have no right, title or interest in or to (a) any trademark, trade dress, brand mark, services mark, trade name, brand name, logo or other similar business symbol of AstraZ-eneca or its Affiliates ... including the trademark Nexium® or any trade dress of any Nexium® product or (b) any know-how, trade secrets, copyrights or other intellectual property of AstraZene-ca or its Affiliates ..., except the limited rights expressly provided for herein.

(Id.) The Agreement “may be enforced by [plaintiffs] ... as permitted by the [its] terms” and the District of New Jersey “retain[ed] jurisdiction to enforce or supervise performance under [the Agreement].” (D.I. 73 at 2)

A month after defendant began marketing the generic product, plaintiffs filed the instant action in the District of Delaware against defendant alleging trademark infringement, counterfeiting, unfair competition, inter aha, for its use of the color purple on the generic drug capsules. (D.I. 69 at 3) Defendant counters that, under the terms of the Agreement, plaintiffs permitted defendant to use the color purple. (D.I. 73 at 3) In November 2015, the court granted plaintiffs’ motions for a temporary restraining order (“TRO”) and preliminary injunction. (D.I. 31) Therein, applying New Jersey contract law, the court concluded that the Agreement addressed only ANDA issues and the plain language protected plaintiffs’ trademark rights. (Id. at 10-11) Defendant appealed the decision and the trademark action was stayed.4 (D.I. 69 at 4)

[749]*749In April 2016, defendant voluntarily dismissed the appeal and the court lifted the stay. (D.I.

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Bluebook (online)
209 F. Supp. 3d 744, 2016 U.S. Dist. LEXIS 94440, 2016 WL 3946799, Counsel Stack Legal Research, https://law.counselstack.com/opinion/astrazeneca-ab-v-dr-reddys-laboratories-inc-ded-2016.