ImprimisRx, LLC v. OSRX, Inc.; Ocular Science, Inc.

District Court, S.D. California·Decided May 20, 2026·No. 3:21-cv-01305·Unknown

Opinion

UNITED STATES DISTRICT COURT

IMPRIMISRX, LLC, Case No. 21-cv-01305-BAS-DDL

Plaintiff, ORDER: v. (1) DENYING DEFENDANTS’ REQUEST FOR ATTORNEYS’ FEES UNDER THE LANHAM OSRX, INC.; OCULAR SCIENCE, INC., ACT; AND Defendants. (2) DENYING WITHOUT PREJUDICE DEFENDANTS’ REQUEST FOR ATTORNEYS’ FEES UNDER THE COPYRIGHT ACT

(ECF No. 385)

Presently before the Court is Defendants OSRX, Inc. and Ocular Science, Inc.’s Motion for Attorneys’ Fees. (Mot., ECF No. 385.) Defendants argue they are entitled to $3,013,183.82 in fees under the Lanham Act and the Copyright Act. (Id.) Plaintiff ImprimisRx, LLC opposes. (Opp’n, ECF No. 405.) The Court finds this Motion suitable for determination on the papers submitted and without oral argument. See Fed. R. Civ. P. 78(b); Civ. L.R. 7.1(d)(1). For the reasons explained below, the Court denies Defendants’ request for fees under the Lanham Act. Further, the Court denies without prejudice Defendants’ request for fees under the Copyright Act. I. BACKGROUND1 Plaintiff ImprimisRx, LLC and Defendants OSRX, Inc. and Ocular Science, Inc. are competitors. They operate compounding pharmacies that focus on medications used in optometry and ophthalmology. Compounding is the practice of combining, mixing, or altering ingredients of an existing drug to create a product tailored to the needs of a specific patient. The parties have a history of litigation. In 2016, Plaintiff sued Ocular Science over its use of an eyedrop brand called Droplet, which Plaintiff claimed was similar to its brand named Dropless. At that time, Ocular Science was also using two compounding formulas for eyedrops known as Pred-Moxi and Dex-Moxi. Plaintiff was attempting to patent the formulations for these eyedrops. Ultimately, the parties settled their prior dispute. They resolved that if Plaintiff was successful at patenting the eyedrop formulations, Ocular Science would stop manufacturing the formulas, and thus, would not use the associated eyedrop names—Pred- Moxi and Dex-Moxi. Further, Ocular Science would pay Plaintiff twenty percent of the revenue on sales of these products up until the time Ocular Science stopped using the two formulations. Unfortunately, the U.S. Patent and Trademark Office did not issue the requested patents. Therefore, Ocular Science not only continued to use the formulations for its eyedrops and the associated names, but it also added more compounding formulas. Plaintiff later filed this suit against Ocular Science and OSRX, Inc., arising from Defendants’ eyedrop sales and unfair competition.

1 The Court incorporates its summary of the parties’ dispute from the Order Denying Defendants’ Renewed Motion for Judgment as a Matter of Law and Granting Remittitur (“Remittitur Order”). (ECF A. Causes of Action Plaintiff brought six claims against Defendants. (Third Am. Compl. ¶¶ 45–91, ECF No. 145.) To start, there were three claims arising under the Lanham Act. In Count One, Plaintiff sued Defendants for false advertising. (Id. ¶¶ 45–53.) Plaintiff alleged that Defendants made misleading statements regarding the safety and efficacy of their compounded drugs. (Id.) In Count Two, Plaintiff claimed Defendants infringed upon Plaintiff’s trademarked names for various compounded eyedrops. (Id. ¶¶ 54–64.) In Count Three, Plaintiff claimed that because Defendants used Plaintiff’s trademarks, Defendants falsely suggested that their eyedrops were made by or connected to Plaintiff. (Id. ¶¶ 65– 74.) In addition, in Count Five, Plaintiff brought a claim under the Copyright Act. (Third Am. Compl. ¶¶ 81–86.) Plaintiff alleged it copyrighted an “Order Form” for its products. (Id. ¶ 82, see also id. ¶ 44.) Further, Plaintiff contended Defendants “copied the Order Form without permission and thus infringed” upon the copyright. (Id. ¶ 83.) Finally, Plaintiff sought redress under California state law through two causes of action. In Count Four, Plaintiff claimed Defendants engaged in common law unfair competition by using Plaintiff’s trademarks. (Third Am. Compl. ¶¶ 75–80.) And in Count Six, Plaintiff pled a violation of California’s Unfair Competition Law, Cal. Bus. & Prof. Code § 17200, based on its other allegations. (Id. ¶¶ 87–91.) Defendants also filed counterclaims. (Answer to Third Am. Compl. & Countercls., ECF No. 152.) Most of these counterclaims were styled as requests for declaratory relief, such as for a determination that Plaintiff’s marks are generic or that no unfair competition occurred. (See id. at 23:1–27:22.) Defendants, however, also brought one counterclaim for false advertising in violation of the Lanham Act based on Plaintiff’s statements about its own products. (Id. at 27:23–28:22.) B. Summary Judgment The parties filed cross-motions for partial summary judgment. Much of the Court’s Summary Judgment Order focused on the competing false advertising claims. The Court initially explained that, ordinarily, the Federal Food, Drug, and Cosmetic Act (“FDCA”) requires drug makers to obtain approval to sell pharmaceutical products under extended, rigorous approval guidelines. (Summ J. Order at 2:16–18, ECF No. 266.) Sections 503A and 503B of the FDCA provide exceptions from those approval guidelines for compounded drugs under certain conditions. (Id. at 2:18–20.) There are two versions of compounding pharmacies under these exceptions: (1) Section 503A pharmacies, which fill prescriptions for individual patients, and (2) Section 503B pharmacies, which produce compounded products in large quantities that are not necessarily tied to a specific patient. (Id. at 2:20– 23.) Plaintiff operates both a Section 503A pharmacy and a Section 503B pharmacy. Defendants operate only a Section 503A pharmacy. (Id. at 2:23–25.) In analyzing the parties’ competing claims, the Court first considered Plaintiff’s assertion that Defendants engaged in false advertising by, among other things, claiming that they operate in compliance with Section 503A of the FDCA. (Summ J. Order at 4:2– 9.) The Court found there were disputed issues of fact with respect to the falsity, deception, and materiality elements of Plaintiff’s false advertising claim. (Id. at 10:24–16:11.) That said, the Court concluded Defendants were entitled to summary adjudication of the injury element of the false advertising claim. (Id. at 16:23–21:18.) The Court reasoned that Plaintiff offered “no evidence it was actually injured by Defendants’ alleged misstatements,” such as evidence showing Plaintiff lost sales due to the contested misstatements. (Id. at 20:5–9.) Consequently, the Court granted Defendants’ motion as to Plaintiff’s Count One for false advertising under the Lanham Act. (Id. at 27:10–12.) Plaintiff’s remaining Lanham Act, Copyright Act, and California state law claims survived for trial. (Id. at 27:12–15.) The Court then considered Plaintiff’s parallel request for summary judgment against Defendants’ false advertising counterclaim. This claim was based on Plaintiff’s statements that it is “compliant with highest quality standards” and is “100% dedicated to patient safety and regulatory compliance.” (See Summ. J. Order at 4:14–26.) The Court found Defendants’ counterclaim could not survive summary judgment for similar reasons as Plaintiff’s false advertising claim. (See id. at 25:14–26:4.) Defendants did “not submit any documentary evidence or deposition evidence demonstrating they lost customers due to Plaintiff’s alleged false advertisements.” (Id. at 26:21–23.) Therefore, the Court granted Plaintiff’s motion with respect to Defendants’ counterclaim for false advertising under the Lanham Act. (Id. at 27:17–19.) C. Trial As the case approached trial, the parties lodged their Proposed Pretrial Order under the Civil Local Rules. (See ECF No. 410, at Attach. 1

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ImprimisRx, LLC v. OSRX, Inc.; Ocular Science, Inc., (S.D. Cal. 2026).

ImprimisRx, LLC v. OSRX, Inc.; Ocular Science, Inc. (ImprimisRx, LLC v. OSRX, Inc.; Ocular Science, Inc.) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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