Missouri Failed to Collect $12.2M in Medicaid Drug Rebates
Summary
The HHS Office of Inspector General (OIG) found that Missouri failed to collect $12.2 million in federal rebates for Medicaid physician-administered and pharmacy drugs between January 1, 2019, and December 31, 2022. The OIG recommends Missouri refund the federal government $9.7 million for physician-administered drugs and $2.5 million for pharmacy drugs.
What changed
The HHS Office of Inspector General (OIG) issued a report detailing that Missouri failed to invoice and collect $12.2 million in federal rebates from manufacturers for Medicaid physician-administered and pharmacy drugs during the audit period of January 1, 2019, to December 31, 2022. This includes $9.7 million for physician-administered drugs and $2.5 million for pharmacy drugs, as well as an additional $165,783 for other physician-administered drugs. The OIG also noted that Missouri did not implement previous audit recommendations.
The OIG recommends that Missouri refund the federal government $9.7 million for physician-administered drugs and $2.5 million for pharmacy drugs. Missouri is also advised to work with CMS to determine the unallowable portion of the $165,783 and resolve previous audit recommendations. While Missouri did not explicitly concur or nonconcur with all recommendations, it indicated corrective actions taken and planned. Compliance officers should note the significant financial implications of failing to adhere to Medicaid drug rebate requirements.
What to do next
- Refund $9.7 million (Federal share) for physician-administered drugs to the Federal Government.
- Obtain rebates for, and refund to the Federal Government, $2.5 million (Federal share) for pharmacy drugs.
- Work with CMS to resolve previous audit recommendations and determine eligibility for $165,783 in potential rebates.
Penalties
Missouri is required to refund $12.2 million (Federal share) to the Federal Government.
Source document (simplified)
Missouri Did Not Obtain Millions of Dollars in Rebates for Medicaid Physician-Administered and Pharmacy Drugs
Issued on
02/11/2026
| Posted on
02/13/2026
| Report number: A-07-23-06113
Report Materials
Why OIG Did This Audit
- For a covered outpatient drug to be eligible for Federal reimbursement under the Medicaid program’s drug rebate requirements, manufacturers must pay rebates to the States for the drugs.
- States invoice the manufacturers for rebates to reduce the cost of drugs to the program.
- This audit is a followup to a previous OIG audit, which reported that between January 1, 2009, and December 31, 2011, Missouri did not always comply with Federal Medicaid requirements for billing manufacturers for rebates for physician-administered drugs.
- This audit, one of a series of OIG audits of the Medicaid drug rebate program, sought to determine whether Missouri complied with Federal Medicaid requirements for invoicing manufacturers for rebates for physician-administered and pharmacy drugs.
What OIG Found
- Between January 1, 2019, and December 31, 2022 (audit period), Missouri did not invoice for, and collect from manufacturers, rebates for $9.7 million (Federal share) for physician-administered drugs and $2.5 million (Federal share) for pharmacy drugs.
- Also, during our audit period, Missouri did not invoice manufacturers for rebates for $165,783 (Federal share) for other physician-administered drugs that could have been eligible for rebates.
- Furthermore, Missouri did not implement our previous audit recommendations.
What OIG Recommends
We make six recommendations to Missouri, including that it refund to the Federal Government $9.7 million (Federal share) for physician-administered drugs and obtain rebates for, and refund to the Federal Government, $2.5 million (Federal share) for pharmacy drugs. We also recommend that Missouri work with CMS to determine the unallowable portion of the $165,783 (Federal share) for claims for other physician-administered drugs that may have been required to be rebated; that it work with CMS to resolve all of our previous audit recommendations; and that it strengthen internal controls. The full recommendations are in the report.
Missouri stated that it would work with CMS to resolve our recommendation regarding the $165,783 (Federal share) for claims for other physician-administered drugs that may have been required to be rebated. Missouri did not indicate concurrence or nonconcurrence with our other recommendations but described corrective actions it had taken and planned to take.
Report Type Audit HHS Agencies Centers for Medicare and Medicaid Services Issue Areas Financial Stewardship Prescription Drug Target Groups – Financial Groups Medicaid
Notice
This report may be subject to section 5274 of the National Defense Authorization Act Fiscal Year 2023, 117 Pub. L. 263.
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