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Bausch & Lomb v. Slayback Pharma — Brimonidine Patent Consolidation | PatSnap
Patent Litigation

Bausch & Lomb v. Slayback Pharma: Brimonidine Patent Case Consolidated in 8 Days

Bausch & Lomb, Bausch & Lomb Ireland Limited, and Eye Therapies, LLC filed suit against Slayback Pharma and Dr. Reddy's Laboratories in New Jersey District Court over US11833245B2, covering Brimonidine Tartrate Ophthalmic Solution 0.025%. Within 8 days, the court ordered consolidation into the existing lead case, Civil Action No. 21-16766.

Resolution time
8days
From filing to consolidation order — one of the shortest docket lifecycles in ANDA-related pharma litigation
Patents asserted
1
US11833245B2 — Brimonidine Tartrate Ophthalmic Solution 0.025%, ophthalmic drug formulation patent
Outcome
Case Consolidated
Merged into lead case Civil Action No. 21-16766; no independent merits disposition on this docket
Cost ruling
Not recorded
No cost or fee ruling recorded in this docket prior to consolidation order
Published by PatSnap Insights Team · Verified by PatSnap Eureka Data
Case overview

Pharma patent consolidation: Brimonidine Tartrate dispute merged into lead case

On December 5, 2023, Bausch & Lomb, Inc., Bausch & Lomb Ireland Limited, and Eye Therapies, LLC filed an infringement action in the U.S. District Court for the District of New Jersey against Slayback Pharma LLC, Slayback Pharma India LLP, Dr. Reddy's Laboratories SA, and Dr. Reddy's Laboratories, Inc. The suit asserted US11833245B2, a patent covering Brimonidine Tartrate Ophthalmic Solution 0.025%, a topical ophthalmic product used for the temporary relief of redness of the eye.

The recorded basis of termination is 'Case Consolidated.' The docket order stipulated that Civil Action No. 21-16766 shall serve as the lead case, directed the Clerk to close Civil Action No. 23-22906, and extended the defendants' deadline to respond to the complaint alleging infringement of the '245 patent to January 19, 2024. All future filings were directed to the lead case docket only.

The consolidation occurred just 8 days after filing, suggesting this action was filed as a companion or related case to already-pending litigation against the same or overlapping defendants. The substantive merits of the infringement claims remain to be litigated within Civil Action No. 21-16766. The specific terms of any underlying agreements between the parties are not disclosed in the available record for this docket.

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Case at a glance
CourtNew Jersey District Court
JudgeN/A
FiledDecember 5, 2023
ClosedDecember 13, 2023
Duration8 days
OutcomeCase Consolidated
Verdict causeInfringement Action
BasisCase Consolidated
Prior Art Intelligence
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Case data sourced from PACER / New Jersey District Court via PatSnap Eureka Litigation Intelligence Explore similar cases ↗
Case timeline

Filing to Case Consolidated in 8 days

From filing to consolidation order — one of the shortest docket lifecycles in ANDA-related pharma litigation

Case timeline: Complaint filed DEC 5 2023 — 8 days total Horizontal timeline showing the three key events in Bausch & Lomb, Inc. v Slayback Pharma, LLC from filing to resolution. Source: PACER, New Jersey District Court. DEC 5 2023 Complaint filed Pre-trial proceedings DEC 13 2023 Case Consolidated 8 DAYS TOTAL
Patent at issue

US11833245B2 — Brimonidine Tartrate Ophthalmic Solution 0.025%

Publication No.US11833245B2
Application No.US18/103404
Patent details
ProductBrimonidine Tartrate Ophthalmic Solution 0.025% for topical ocular use
Cited in actionDecember 5, 2023
Technical brief · sourced from PatSnap patent database
Patent figurePatent figure
Representative claim (1 of 2 independent)
1. A method for reducing eye redness in a human subject having ocular hyperemia, consisting of topically administering to an eye of said human in need of said reduction of eye redness a composition in the form of an ocular drop consisting of 0.025% weight by volume brimonidine as the sole active ingredient, and one or more non-therapeutic components including benzalkonium chloride, wherein the ocular drop has a pH between 5.5 to 6.5, wherein the ocular hyperemia is reduced.
Technical background
CROSS REFERENCE TO RELATED APPLICATIONS This application is a continuation of U.S. patent application Ser. No. 17/585,395, filed on Jan. 26, 2022, which is a continuation of U.S. patent application Ser. No. 17/476,104, filed Sep. 15, 2021, which is a continuation of U.S. patent application Ser. No. 16/179,261 filed Nov. 2, 2018, which is a continuation of U.S. patent application Ser. No. 12/460,967 filed Jul. 27, 2009, which claims priority to U.S. Provisional Application Ser. No. 61/137,714, filed Aug. 1, 2008; 61…
Patent family
47 family members across 21 jurisdictions (US, IT, SI, EP, CA, JP, CY, WO, NO, DK, ES, AT)
PatSnap Eureka · FTO Search Agent
Should you run an FTO analysis against US11833245B2?

Any pharmaceutical company, generic manufacturer, or contract development organisation working on Brimonidine Tartrate ophthalmic formulations — particularly at or near 0.025% concentration — faces active enforcement risk from US11833245B2. With multiple defendants already named and consolidated into ongoing litigation in New Jersey, the patent holders have demonstrated willingness to pursue parallel infringement actions. An FTO analysis is warranted before advancing an ANDA filing or product launch in this category.

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Official verdict

Official order — verbatim text

STIPULATION ANDORDERConsolidating cases; CivilActionNo. 21-16766 shall bethelead caseand allfilings going forward shall be madeinCivilActionNo. 21-16766 only; Directing the Clerk to close CivilActionNo. 23-22906; ExtendingDefendants' deadlineto respond to Plaintiff's Complaint alleging infringement of the'245 patent to January 19, 2024
Source: PACER Docket, Case 3:23-cv-22906, New Jersey District Court

The court's stipulation and order consolidated this newly filed case into the existing lead docket, Civil Action No. 21-16766, within 8 days of filing. The order directs closure of this docket and grants defendants an extended answer deadline, but makes no merits determination on infringement of US11833245B2. The substantive dispute over Brimonidine Tartrate Ophthalmic Solution 0.025% continues in the lead case.

PACER case 3:23-cv-22906 · Public docket record Explore in Eureka ↗

Case transfer / consolidation

What case consolidation means for this docket

Consolidation under Federal Rule of Civil Procedure 42(a) allows a court to combine cases sharing common questions of law or fact. Here, the New Jersey District Court ordered this action merged into the existing lead case, Civil Action No. 21-16766. This docket is administratively closed; all substantive proceedings, filings, and rulings now occur exclusively in the lead case.

Merged into 21-16766
Venue and docket implications

Same court, single docket — no venue change

Unlike a transfer under 28 U.S.C. § 1404, consolidation here kept the case within the District of New Jersey. The parties, claims, and patent at issue remain the same; only the docket number changes. Practitioners should monitor Civil Action No. 21-16766 for all scheduling orders, claim construction proceedings, and merits rulings going forward.

District of New Jersey retained
Defendants' procedural position

Response deadline extended to January 19, 2024

As part of the consolidation order, defendants' deadline to respond to the complaint alleging infringement of the '245 patent was extended to January 19, 2024. This extension is consistent with standard practice when cases are consolidated close to filing, providing defendants adequate time to respond within the unified lead-case framework rather than on the compressed original schedule.

Answer deadline: Jan 19, 2024
What happens next

Merits to be decided in the lead case proceeding

With this docket closed, all infringement claims regarding US11833245B2 and Brimonidine Tartrate Ophthalmic Solution 0.025% will be adjudicated in Civil Action No. 21-16766. Stakeholders — including competing generic manufacturers and patent challengers — should track that lead case for claim construction, summary judgment, and trial scheduling relevant to this ophthalmic formulation patent.

Track Civil Action 21-16766
Legal analysis based on PACER docket records for case 3:23-cv-22906 and PatSnap Eureka litigation intelligence Search PatSnap Eureka ↗
Parties and representation

Full party and counsel information

RoleNameTypeDetail
PlaintiffBausch & Lomb, Inc.Company/Search in Eureka ↗
Co-PlaintiffBausch & Lomb Ireland LimitedIndividualSearch in Eureka ↗
Co-PlaintiffEye Therapies, LLCCompanySearch in Eureka ↗
DefendantSlayback Pharma, LLCCompany/Search in Eureka ↗
Co-DefendantDr. Reddys Laboratories, SACompanySearch in Eureka ↗
Co-DefendantDr. Reddy's Laboratories, Inc.CompanySearch in Eureka ↗
Co-DefendantSlayback Pharma India, LLPCompanySearch in Eureka ↗
Plaintiff counselBryan C. DinerAttorneyCounsel for Bausch & Lomb, Inc.Search in Eureka ↗
Plaintiff counselJ. BRUGH LOWERAttorneyCounsel for Bausch & Lomb, Inc.Search in Eureka ↗
Plaintiff counselJustin James HasfordAttorneyCounsel for Bausch & Lomb, Inc.Search in Eureka ↗
Plaintiff counselWilliam P. Deni , Jr.AttorneyCounsel for Bausch & Lomb, Inc.Search in Eureka ↗
Plaintiff law firmFinnegan, Henderson, Farabow, Garrett & Dunner, LLPLaw FirmRepresenting Bausch & Lomb, Inc.Search in Eureka ↗
Plaintiff law firmGibbons PCLaw FirmRepresenting Bausch & Lomb, Inc.Search in Eureka ↗
Presiding judgeJudge N/AJudgeNew Jersey District CourtSearch in Eureka ↗
R&D signals

R&D signals in the ophthalmic formulation patent space

Forward-looking patent and R&D intelligence derived from Bausch & Lomb's enforcement of US11833245B2 across the Brimonidine Tartrate and ophthalmic drug delivery landscape.

Patent portfolio

Bausch & Lomb's ophthalmic formulation patent activity

Bausch & Lomb's decision to enforce US11833245B2 alongside co-plaintiff Eye Therapies, LLC suggests a layered patent portfolio strategy around Brimonidine Tartrate ophthalmic products. Monitoring their broader filing activity in alpha-2 adrenergic agonist formulations and ophthalmic delivery systems may reveal additional IP barriers relevant to generic and branded competitors in this category.

Bausch & Lomb IP portfolio
Technology landscape

Filing trends in Brimonidine Tartrate ophthalmic formulations

The ophthalmic redness-relief segment is an active IP filing area, with innovators and generics competing on formulation parameters such as concentration, preservative systems, and excipient profiles. Tracking patent filings around Brimonidine Tartrate 0.025% and closely related ophthalmic alpha agonist formulations can surface white-space opportunities or emerging barriers ahead of regulatory filings.

Brimonidine ophthalmic filing trends
Competitor IP posture

Slayback Pharma and Dr. Reddy's ophthalmic patent positions

As defendants in this consolidated ANDA action, Slayback Pharma and Dr. Reddy's Laboratories are active players in the generic ophthalmic pharmaceutical space. Analysing their own patent filings, ANDA paragraph IV certifications, and R&D pipelines in ophthalmic formulations can reveal competitive positioning and potential design-around strategies in the Brimonidine category.

Generic ophthalmic IP landscape
White space opportunity

Adjacent ophthalmic redness-relief formulation opportunities

The enforcement perimeter around Brimonidine Tartrate 0.025% may create white-space opportunities in alternative concentrations, novel excipient combinations, or differentiated delivery mechanisms for ophthalmic redness relief. Mapping the claim boundaries of US11833245B2 against adjacent formulation space can help R&D teams identify patentable differentiation pathways that avoid the existing IP perimeter.

Ophthalmic formulation white space
Related litigation

Similar ophthalmic drug patent cases in New Jersey District Court

Explore related ANDA infringement actions involving ophthalmic formulation patents litigated in the District of New Jersey, including other Brimonidine Tartrate and alpha-2 agonist cases.

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Bausch & Lomb, Inc. patent enforcement history, New Jersey District Court case history, Bausch & Lomb, Inc.'s full IP portfolio, and comparable case analysis
Brimonidine ANDA cases NJBausch & Lomb enforcement historyDr. Reddy's ophthalmic patent disputesSlayback Pharma litigation record
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Strategic implications

What this case signals for the ophthalmic pharma IP landscape

A consolidation after 8 days signals coordinated, multi-defendant enforcement of the Brimonidine Tartrate '245 patent by Bausch & Lomb.

Multi-defendant enforcement strategy signals broad patent perimeter defence

Filing against both Slayback Pharma and Dr. Reddy's Laboratories simultaneously — then consolidating — is consistent with a coordinated ANDA litigation strategy. Companies in the generic ophthalmic space should monitor both defendants' ANDA filings and the lead case docket for claim scope developments that could affect their own market-entry timelines.

US11833245B2 remains actively enforced — FTO exposure is real

The consolidation does not resolve the infringement claims; it centralises them. Any generic manufacturer developing or seeking approval for a Brimonidine Tartrate ophthalmic formulation at 0.025% concentration should treat this patent as an active enforcement risk and conduct a current freedom-to-operate analysis against the '245 patent claims.

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Full strategic analysis in PatSnap Eureka
Unlock deeper intelligence on ANDA ophthalmic patent enforcement strategies and the District of New Jersey's consolidation case outcomes.
Licensing structure signalsLead case claim constructionGeneric market-entry risk
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Analysis powered by PatSnap Eureka Litigation Intelligence Explore in Eureka ↗
Frequently asked questions

Bausch v Slayback — key questions answered

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Monitor the Brimonidine Tartrate patent dispute in real time

US11833245B2 remains actively litigated in Civil Action No. 21-16766. Use PatSnap Eureka to track claim construction rulings, new filings, and enforcement signals across the Bausch & Lomb ophthalmic patent portfolio before your next product or ANDA decision.

Disclaimer

This page is compiled from public court dockets and third-party patent and litigation data via PatSnap Eureka, and is provided for general informational purposes only. The information shown — including party names, patent and application numbers, dates, case status, outcomes, and any analysis — may be incomplete, may not reflect the most recent filings or legal status, and may contain errors or omissions. Verify all details against official court records (for example, PACER) and the relevant patent office before relying on them.

Nothing on this page constitutes legal advice or a legal opinion on the validity, infringement, enforceability, or scope of any patent or case, and no attorney‑client relationship is created by its use. Any description of an outcome (such as a dismissal, settlement, or consent judgment) is a general summary, not a legal determination. All patents, trademarks, and company or law‑firm names are the property of their respective owners. PatSnap makes no warranty as to the accuracy or completeness of this content and disclaims, to the fullest extent permitted by law, all liability for reliance on it. For advice on a specific matter, consult qualified legal counsel.

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