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Program Releases

The Centers for Medicare & Medicaid Services (CMS) issues program releases to states and drug manufacturers participating in the Medicaid Drug Rebate Program. To find prior releases by topic, please use the "Keyword Search" function below.

To further refine your search, we have also posted a Division of Pharmacy Releases Index, which is a compilation of all the State and Manufacturer Releases topics from 1991 to Present. Please download a copy for your reference.

If you have any questions regarding the states and/or drug manufacturer releases, please email MDROperations@cms.hhs.gov.

Disclaimer: Please note that the information provided on this web page does not bind or obligate the Centers for Medicare and Medicaid Services (CMS).  The statements included on this web page are intended to provide information on Medicaid Drug Rebate Program Releases and do not in any way revise or modify the requirements set forth in Section 1927 of the Act, the national drug rebate agreement (NDRA), or regulations.

Page Last Updated on July 3, 2024

Showing 31 to 40 of 120 results

Manufacturer Release 090

Date:
Type: Manufacturer Release
Keywords: Baseline Data, Buying a Drug, Sale of Authorized Generics, Branded Prescription Drug Fees
Links: Manufacturer Release 090: Reporting Baseline Data; Buying a Drug from another Manufacturer; Buying a Drug but Not Changing the NDC; Buying a Drug and Changing the NDC; Sale of Authorized Generic Drugs; 2012 State Utilization Data for BPD Fees ( PDF, 146.23 KB )
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Manufacturer Release 089

Date:
Type: Manufacturer Release
Keywords: 2012 State Utilization data for BPD fees, Using CMS form 304 (Rosi) and CMS form 304A (PQAS) format, Clarification of postmark dates of calculating interest
Links: Manufacturer Release 089: 2012 State Utilization Data for Branded Prescription Drug (BPD) Fees; Clarification of Postmark Dates for Purposes of Calculating Interest; DESI Code Correction; Retirement News ( PDF, 156.32 KB )
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Manufacturer Release 088

Date:
Type: Manufacturer Release
Keywords: Coverage of Barbiturates, Benzodiazepines, All Drugs Used for Smoking Cessation, 2014
Links: Manufacturer Release 088: Coverage of Barbiturates, Benzodiazepines, and all Drugs Used for Smoking Cessation Effective January 1, 2014; Medicaid Beneficiaries; Dual Eligible Beneficiaries; State Plan Amendments ( PDF, 135.49 KB )
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Manufacturer Release 087

Date:
Type: Manufacturer Release
Keywords: FDA Listing of Products in MDRP, Listing Status of Products with FDA, Products not Listed with FDA
Links: Manufacturer Release 087: Products in the Medicaid Drug Rebate Program (MDRP) that are not listed with FDA ( PDF, 141.33 KB )
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Manufacturer Release 086

Date:
Type: Manufacturer Release
Keywords: Monthly AMP Units, AMP Units
Links: Manufacturer Release 086: Reporting Average Manufacturer Price (AMP) Units ( PDF, 301.62 KB )
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Manufacturer Release 085

Date:
Type: Manufacturer Release
Keywords: Clotting Factor and Exclusively Pediatric Indicators, ESRD Bundled Services, 340B Program
Links: Manufacturer Release 085: OIG Report: 340B Purchased Drugs; Rebate Clarification for ESRD Bundled Services; Clotting Factor/Exclusively Pediatric Indicators Applied in the MDR and DDR Systems ( PDF, 153.01 KB )
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Manufacturer Release 084

Date:
Type: Manufacturer Release
Keywords: MCO Rebate Guidance, Reconciliation of State Invoice Form Use, Prior Quarter Adjustment Statement Form Use, Invoices - CMS R-144 (State Invoice) Changes, Electronic Listing of Products with FDA
Links: Manufacturer Release 084: Updating Drug Information Electronically with FDA; Revision of CMS Forms 394/304a to Include a “FFS/MCO Record ID” Column; Guidance on Manufacturers Paying Rebates for Medicaid MCO Enrollees ( PDF, 158.97 KB )
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Manufacturer Release 083

Date:
Type: Manufacturer Release
Keywords: AMP - Lagged Price/Smoothing, AMP Smoothing Process
Links: Manufacturer Release 083: AMP Smoothing Process ( PDF, 79.32 KB )
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Manufacturer Release 082

Date:
Type: Manufacturer Release
Keywords: AMP - Monthly AMP Units & File Record Layout, Penalty for Untimely & False Reporting, Unit Type - Reporting, Units Per Package Size (UPPS), Drug Category Change/Reporting
Links: Manufacturer Release 082: Incorrect Product information Reported; Unit Type/UPPS; Drug Category/FDA Approval Date; Penalties for Failure to Provide Timely Information and False Information; File Format Change to Collect Monthly AMP Units ( PDF, 332.43 KB )
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Manufacturer Release 081

Date:
Type: Manufacturer Release
Keywords: Active Pharmaceutical Ingredient & Excipient Removal, Affordable Care Act (ACA), Failure to Submit Pricing Timely, Dispute Resolution Issues - E-Mail Address/Contacts
Links: Manufacturer Release 081: ACA Op Guidance/1Q2010 Rebate; URA Calculation; Rebate Calculation S/I Line Extension Drugs; Rebate Amount for S/I Drugs; Pediatric/Clotting Factor Drugs; Removal of APIs/Excipients as CODs; Failure to Submit AMP Timely ( PDF, 376.17 KB )
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