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Medicaid Drug Rebate Program


Created by the Omnibus Budget Reconciliation Act (OBRA) of 1990, the Medicaid Drug Rebate Program requires a drug manufacturer to enter into and have in effect a national rebate agreement with the Secretary of the Department of Health and Human Services for States to receive federal funding for outpatient drugs dispensed to Medicaid patients. The drug rebate program is administered by CMS's Center for Medicaid and State Operations (CMSO). The drug rebate program was amended by the Veterans Health Care Act of 1992. Under VHCA, drug manufacturers are required to enter a pricing agreement with the Secretary of Health and Human Services for the Section 340B Drug Pricing Program, which is administered by the Health Resources and Services Administration. To obtain a copy of this pricing agreement, please use this website: ftp://ftp.hrsa.gov/bphc/pdf/opa/pricingagreement.pdf. In addition, VHCA requires drug manufacturers to enter into various agreements with the Department of Veterans Affairs. For more information regarding Section 603 of the VHCA's requirements, please contact Carole O'Brien at (708)786-4957 or carole.obrien@med.va.gov. A drug manufacturer must sign an agreement with these two programs in order to have its drugs covered by Medicaid.

Approximately 550 pharmaceutical companies currently participate in this program. Forty nine States, (Arizona is excluded), and the District of Columbia cover drugs under the Medicaid Drug Rebate Program.

As of January 1, 1996, the rebate for covered outpatient drugs is as follows:

Innovator Drugs - the larger of 15.1 % of the Average Manufacturer Price (AMP) per unit or the difference between the AMP and the best price per unit and adjusted by the CPI-U based on launch date and current quarter AMP.

Non-innovator Drugs - 11 % of the AMP per unit.


The following information concerning this program is available:

Last Modified on Thursday, September 16, 2004