You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Litigation Details for United States v. Indivior Inc. (W.D. Va. 2019)


✉ Email this page to a colleague

« Back to Dashboard


Small Molecule Drugs cited in United States v. Indivior Inc.
The small molecule drugs covered by the patents cited in this case are ⤷  Start Trial , ⤷  Start Trial , and ⤷  Start Trial .

Details for United States v. Indivior Inc. (W.D. Va. 2019)

Date Filed Document No. Description Snippet Link To Document
2019-04-09 115 Superseding Indictment atentTitle um ber (1) 8,475,832 Sublingualandbuccalfilm compositions …,4718643 b. Patents: Patent P … TheDrugPriceCompetition andPatentTerm RestorationAct(ill-latch-W axman Act'& External link to document
>Date Filed >Document No. >Description >Snippet >Link To Document

Litigation summary and analysis for: United States v. Indivior Inc. (W.D. Va. 2019)

Last updated: February 9, 2026

Litigation Summary and Analysis: United States v. Indivior Inc. | Case No. 1:19-cr-00016-JPJ-PMS-2

Case Overview

United States v. Indivior Inc. involves criminal charges against the pharmaceutical company Indivior Inc., a subsidiary of Indivior PLC, related to the marketing and sales of opioid addiction treatment drugs, specifically Suboxone (buprenorphine/naloxone). Filed in the Western District of Virginia in 2019, the case highlights allegations of misbranding and illegal promotional practices aimed at increasing prescriptions while concealing risks.

Charges and Allegations

Indivior was charged with multiple counts of conspiracy, mail fraud, and violations of the Federal Food, Drug, and Cosmetic Act (FDCA). The core allegations include:

  • Misbranding of Suboxone: The company allegedly promoted higher dosages of Suboxone off-label, despite known risks.
  • Illegal marketing activities: Allegedly incentivized physicians with kickbacks and other inducements to prescribe Suboxone for purposes not approved by the FDA.
  • Concealment of risks: The company purportedly minimized known side effects and risks associated with increased dosages and off-label use.

Key Evidence and Litigation Developments

  • Internal communications: Evidence includes internal emails and memos showing deliberate strategies to boost prescribing practices beyond approved indications.
  • Whistleblower testimony: Several whistleblowers provided affidavits detailing internal practices aimed at circumventing regulatory restrictions.
  • Financial incentives: Data indicates payments to physicians, including trips, consultations, and bonuses tied to prescription volume increases.

Judicial Proceedings

The case proceeded through preliminary motions, discovery, and eventual negotiations. In 2020, Indivior settled with the U.S. Department of Justice (DOJ), avoiding trial on the criminal counts but agreeing to substantial fines:

  • Settlement amount: Approximately $300 million payable over five years.
  • Corporate probation: Indivior agreed to a five-year corporate integrity agreement, including compliance oversight and reporting mechanisms.
  • No admission of guilt: The settlement explicitly states that the company did not admit liability.

Strategic and Policy Impacts

This case exemplifies the DOJ’s focus on holding pharmaceutical companies accountable for marketing practices that may contribute to the opioid epidemic. It reflects increased regulatory scrutiny of opioid manufacturers and distributors, emphasizing:

  • Enhanced compliance protocols.
  • Transparency in marketing and physician incentives.
  • Data-driven enforcement actions.

Implications for Industry

  • Companies involved in opioid manufacturing face heightened regulatory risk.
  • Increased scrutiny extends to marketing practices, requiring robust compliance programs.
  • Settlement sizes have increased, signaling aggressive enforcement strategies.

Industry Comparison

Aspect Indivior Case Typical Pharma Litigation
Settlement Amounts Approximately $300 million Varies; often in hundreds of millions
Focus Areas Off-label marketing, incentivization Off-label use, improper promotion, kickbacks
Court Orders Corporate probation, compliance oversight Varies; often includes fines, monitors

Conclusion

The Indivior case demonstrates a strategic enforcement of regulations surrounding opioid marketing. The significant settlement and probation serve as a warning for pharmaceutical companies to adhere strictly to FDA-approved uses and promotional guidelines.


Key Takeaways

  • Indivior faced criminal charges related to illegal marketing practices for Suboxone.
  • The company settled for $300 million, avoiding criminal trial but accepting oversight and penalties.
  • Evidence centered on internal communications and financial inducements to physicians.
  • The case signals increased regulatory pressure on opioids manufacturers.
  • Companies must ensure compliance to mitigate legal and financial risks.

FAQs

1. What are the main legal violations in United States v. Indivior?
Misbranding of drugs, illegal marketing, and concealment of risks.

2. How does this case affect other pharmaceutical companies?
It raises compliance standards and will likely lead to stricter internal controls and oversight.

3. What did Indivior settle for, and what does the settlement include?
Approximately $300 million; the settlement includes fines and a five-year corporate integrity agreement.

4. Did Indivior admit guilt in the settlement?
No, the settlement explicitly states no admission of liability.

5. What lessons can be drawn from this case regarding pharmaceutical marketing practices?
Strict adherence to FDA guidelines and transparent promotion are critical to avoid legal liabilities.


References

  1. U.S. Department of Justice announcement, 2020

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.