Last Updated: August 4, 2026

Litigation Details for Meda Pharmaceuticals Inc. v. Amneal Pharmaceuticals LLC (D. Del. 2015)


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Small Molecule Drugs cited in Meda Pharmaceuticals Inc. v. Amneal Pharmaceuticals LLC
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Details for Meda Pharmaceuticals Inc. v. Amneal Pharmaceuticals LLC (D. Del. 2015)

Date Filed Document No. Description Snippet Link To Document
2015-07-17 External link to document
2015-07-17 4 the Commissioner of Patents and Trademarks for Patent/Trademark Number(s) 8,071,073; 8,518,919; (aah) (…2015 27 April 2017 1:15-cv-00617 830 Patent None District Court, D. Delaware External link to document
>Date Filed >Document No. >Description >Snippet >Link To Document

Meda Pharmaceuticals Inc. v. Amneal Pharmaceuticals LLC (1:15-cv-00617) Litigation Summary and Patent-Exposure Analysis

Last updated: July 16, 2026

Meda Pharmaceuticals Inc. sued Amneal Pharmaceuticals LLC in a Hatch-Waxman-related patent infringement action in case 1:15-cv-00617. The record indicates a disputes centered on FDA Paragraph IV-type generic entry risk for Meda’s branded product. The available docket information is insufficient to produce a complete, accurate claim-by-claim infringement and invalidity analysis, including asserted patents, specific claims, dispositive rulings, settlement terms, and the final judgment posture.

What does Meda v. Amneal Pharmaceuticals LLC (1:15-cv-00617) litigate?

Answer: A Hatch-Waxman patent infringement case tied to a generic “enter at risk” challenge, brought by Meda against Amneal.

Which product and active ingredient are involved?

Answer: Not determinable from the information provided.

Is this Paragraph IV litigation tied to an ANDA?

Answer: The case style and typical structure of these disputes indicate it is consistent with an ANDA/Paragraph IV framework, but the specific ANDA, listed patents, and FDA submission identifiers are not provided.

Which patents were asserted in Meda v. Amneal (1:15-cv-00617)?

Answer: Not determinable from the information provided.

What is the asserted patent list?

Answer: Not available in the provided dataset.

What is the technology coverage?

Answer: Not available (formulation, polymorph, method-of-use, process, or kit claims cannot be confirmed).

What happened procedurally in Meda v. Amneal (1:15-cv-00617)?

Answer: Not determinable from the information provided.

Key procedural milestones (typical set, status not available)

  • Complaint and service
  • Amneal’s answer and defenses
  • Claim construction (Markman) proceedings
  • Summary judgment motions
  • Bench trial or jury trial schedule (if any)
  • Final judgment date

How did the court rule in Meda v. Amneal (1:15-cv-00617)?

Answer: Not determinable from the information provided.

Disposition type

  • Judgment on the pleadings
  • Summary judgment
  • Dismissal
  • Voluntary dismissal
  • Settlement and stipulation of dismissal

Injunction or final non-infringement/invalidity rulings

Answer: Not available.

Did Meda v. Amneal (1:15-cv-00617) end in settlement?

Answer: Not determinable from the information provided.

Settlement terms that drive generic timing

  • Carve-outs, license scope, and permitted launch dates
  • Dismissal with prejudice or without prejudice
  • Agreement provisions affecting FDA approval timing
  • Ongoing covenant-not-to-sue boundaries

What Orange Book status and exclusivity did this litigation target?

Answer: Not determinable from the information provided.

Patents likely at issue (not confirmed)

  • Drug substance/active ingredient patents
  • Formulation or polymorph patents
  • Method-of-use patents
  • Manufacturing/process patents
  • Pediatric or exclusivity-related extensions

What generic entry risks exist for Amneal if Meda v. Amneal (1:15-cv-00617) concludes adversely?

Answer: Not determinable from the information provided.

Risks typically assessed in this posture

  • Remaining unexpired patents on the Orange Book
  • Barriers from additional listed patents (continuation filings, terminal disclaimers)
  • Impacts from claim construction outcomes
  • Risk of injunction or damages exposure

How does this case affect the competitive landscape?

Answer: Not determinable from the information provided.

Practical impacts typically tracked

  • Entry timing into the relevant NDC market
  • Whether other ANDA filers are delayed by the same patent estate
  • Whether Amneal becomes a preferred licensee or launches at risk

Key Takeaways

1. The docket identifier 1:15-cv-00617 matches a Meda v. Amneal patent infringement dispute.
2. The case is consistent with Hatch-Waxman/Paragraph IV-style generic entry litigation.
3. A complete and accurate litigation summary cannot be produced from the provided inputs because the record excerpt does not include asserted patents, product/NDC linkage, procedural milestones, rulings, or disposition/settlement terms.

FAQs

  1. What court and judge handled Meda v. Amneal (1:15-cv-00617)?
  2. Which Meda Orange Book patents did Amneal challenge in the ANDA tied to 1:15-cv-00617?
  3. Did the court issue a Markman order affecting infringement or noninfringement scope?
  4. Was Amneal’s proposed generic enjoined or permitted to launch during or after 1:15-cv-00617?
  5. Did Meda and Amneal reach a settlement that set launch dates or licensing terms?

References

  1. Meda Pharmaceuticals Inc. v. Amneal Pharmaceuticals LLC, No. 1:15-cv-00617 (docket).

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