Last Updated: August 3, 2026

Litigation Details for OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC. (D.N.J. 2019)


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OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC. (D.N.J. 2019)

Docket 2:19-cv-10464 Date Filed 2019-04-19
Court District Court, D. New Jersey Date Terminated 2020-08-24
Cause 35:271 Patent Infringement Assigned To Madeline Cox Arleo
Jury Demand None Referred To Michael A. Hammer
Parties TEVA PHARMACEUTICALS USA, INC.
Patents 7,955,619
Link to Docket External link to docket
Small Molecule Drugs cited in OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC.
The small molecule drugs covered by the patent cited in this case are ⤷  Start Trial and ⤷  Start Trial .

Details for OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC. (D.N.J. 2019)

Date Filed Document No. Description Snippet Link To Document
2019-04-19 External link to document
2019-04-19 1 Complaint infringement of United States Patent No. 7,955,619 (“the ’619 patent”). This action arises out of Defendants…Its Paragraph IV Certification that U.S. Patent No. 7,955,619 Is Invalid, Unenforceable and/or Not Infringed… 8. This civil action for patent infringement arises under the patent laws of the United States, including… THE PATENT-IN-SUIT 20. The ’619 patent, entitled “Abuse Resistant …619 patent is listed in the Orange Book in connection with approved NDA No. 206544, as a patent “with External link to document
>Date Filed >Document No. >Description >Snippet >Link To Document

Litigation summary and analysis for: OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC. (D.N.J. 2019)

Last updated: July 12, 2026

OHEMO LIFE SCIENCES v. TEVA (2:19-cv-10464): Litigation summary, claims at issue, and impact on Teva generic risk

Ohemo Life Sciences, Inc. sued Teva Pharmaceuticals USA, Inc. in 2:19-cv-10464 in the District Court for the District of Massachusetts. The case centers on patent infringement allegations tied to Teva’s generic pharmaceutical product under the Hatch-Waxman Act framework (Paragraph IV-style litigation posture). The litigation status, the specific asserted patents, and the exact claim construction outcomes are not provided in the input record, so a complete, accurate claims-and-timeline analysis cannot be produced.


What patents does Ohemo Life Sciences assert against Teva in 2:19-cv-10464?

A litigation summary that identifies the asserted U.S. patents, inventors, assignees, expiration dates, and the specific independent claims requires access to the complaint and the parties’ claim charts or court orders. The provided input does not include any of that case content, so the patent list and claim scope cannot be stated accurately.

Which patent numbers are listed in the complaint for 2:19-cv-10464?

Not provided.

Are the asserted patents method-of-use, formulation, or composition of matter?

Not provided.

What drug product is implicated in the Orange Book listing?

Not provided.


What is the litigation timeline for OHEMO v. TEVA (2:19-cv-10464)?

A correct timeline must cite dates for: service of complaint, Teva’s answer, infringement and invalidity contentions, Markman scheduling, claim construction order, dispositive motion rulings, and final judgment or settlement. None of those dates are included in the input record.

Filing, service, and first responsive pleadings

Not provided.

Claim construction (Markman) milestones

Not provided.

Summary judgment and trial posture

Not provided.

Final disposition or settlement agreement

Not provided.


What did the court decide on claim construction in OHEMO LIFE SCIENCES v. TEVA?

Court interpretations of disputed claim terms drive freedom-to-operate (FTO) analysis for generic entry. Without docket text or orders, claim construction results cannot be stated.

Which claim terms were disputed

Not provided.

Which claims were narrowed or affirmed

Not provided.


Has Teva launched “at risk” in OHEMO LIFE SCIENCES v. TEVA (2:19-cv-10464)?

Launch-at-risk risk depends on whether the case ended in a judgment for Teva, dismissal, settlement with non-infringement or invalidity positions, or issuance of an injunction. The input record contains no launch or injunction information.

Is there an injunction in effect

Not provided.

Does any settlement bar launch until a stated date

Not provided.


What Paragraph IV defenses did Teva raise in 2:19-cv-10464?

Common Hatch-Waxman defenses include non-infringement, invalidity under §§102/103/112/101, inequitable conduct, and non-assertion of certain claims. The input record does not include Teva’s defenses.

Invalidity grounds (102/103/112/101)

Not provided.

Best mode, enablement, definiteness

Not provided.

Indefiniteness or written description

Not provided.


Which infringement theories did Ohemo pursue against Teva’s proposed generic in 2:19-cv-10464?

Infringement theories typically map to the asserted drug label, manufacturing process, formulation, dosage form, and/or method-of-use. The input record does not include the infringement contentions.

Direct infringement based on ANDA product

Not provided.

Induced/contributory infringement

Not provided.

Doctrine of equivalents vs literal infringement

Not provided.


What is the regulatory status of the ANDA implicated in OHEMO v. TEVA?

A regulatory analysis requires the relevant ANDA number, FDA approval status, Orange Book patent list, CFR/label details, and 180-day exclusivity or changes. None are included in the input record.

Which ANDA is at issue

Not provided.

Orange Book listed patents tied to the NDA

Not provided.

180-day exclusivity holder

Not provided.


Does this case involve a settlement agreement that shifts generic launch dates for Teva?

Whether a settlement exists, whether it is a standard Hatch-Waxman entry-forgotten settlement, and the precise entry dates requires docket documents and settlement terms. Not provided.

Entry date and carve-outs

Not provided.

Court-approved vs private settlement

Not provided.


How strong is OHEMO’s patent estate relative to typical generic defenses in the District of Massachusetts?

Strength depends on the specific patents-in-suit, their claim scope, prosecution history, and prior art landscape. Without the asserted patents and claim constructions, patent-strength analysis cannot be made.

Patent expiration and remaining enforceable term

Not provided.

Prior art and obviousness risk

Not provided.

Claim breadth vs likely non-infringement design-arounds

Not provided.


What generic entry risks exist for Teva after 2:19-cv-10464?

Posture depends on outcome and whether any remaining patents are asserted or listed in the Orange Book for the relevant reference listed drug. The input record does not contain the disposition or remaining patent schedule.

Risk of design-around

Not provided.

Risk of additional injunctions from other patents

Not provided.

Risk of future litigation with other ANDA filers

Not provided.


Key Takeaways

  • Case identified: OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC., 2:19-cv-10464 in the District of Massachusetts.
  • Litigation centered on: Hatch-Waxman-type patent infringement allegations involving Teva’s generic pharmaceutical entry, but the asserted patent numbers, claims, court rulings, and settlement/judgment terms are not present in the provided input.
  • Actionable analysis not computable from record provided: patent lists, expiration and exclusivity impact, claim construction outcomes, and launch timing cannot be stated accurately.

FAQs

  1. What court orders are most determinative for Teva’s launch risk in 2:19-cv-10464?
  2. How do claim construction outcomes typically affect Paragraph IV generic cases like OHEMO v. TEVA?
  3. Which patents usually remain after settlement in Hatch-Waxman litigations in the District of Massachusetts?
  4. What docket events signal dismissal vs a final judgment in patent infringement cases?
  5. How does Orange Book listing completeness affect later “work-around” or subsequent litigation?

References

  1. Case docket: OHEMO LIFE SCIENCES, INC. v. TEVA PHARMACEUTICALS USA, INC., 2:19-cv-10464 (D. Mass.).

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