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<classification authority="sudocs">GA 1.13:GAO-07-481T</classification>
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 <subject>Beneficiaries</subject>
 <subject>Congressional oversight</subject>
 <subject>Medicaid</subject>
 <subject>Medicare</subject>
 <subject>Pharmaceutical industry</subject>
 <subject>Prescription drugs</subject>
 <subject>Prices and pricing</subject>
 <subject>Program abuses</subject>
 <subject>Program evaluation</subject>
 <subject>Executive agency oversight</subject>
 <subject>Transparency</subject>
 <subject>340B Drug Pricing Program</subject>
 <subject>Medicaid Drug Rebate Program</subject>
 <subject>Medicare Part D</subject>
 <type>Testimony</type>
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<titleInfo>
 <title>Prescription Drugs: Oversight of Drug Pricing in Federal Programs</title>
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<abstract>Several federal programs help pay for or reduce the costs of
prescription drugs for eligible individuals and entities. Three  
examples are the Medicaid drug rebate program, part of the joint 
federal-state Medicaid program that finances medical services for
certain low-income people; the 340B drug pricing program, which  
provides discounted drug prices to certain eligible entities such
as community health centers; and the Medicare Part D program,	 
which provides a Medicare drug benefit for the elderly and	 
certain disabled people. The price information drug manufacturers
report under these federal programs affects related federal	 
spending. Spending is also affected by the extent to which	 
federal oversight ensures the accuracy of this information. GAO  
was asked to provide information related to the oversight of	 
prescription drug pricing practices that affect these federal	 
programs. This testimony focuses on the oversight of drug pricing
related to the three programs and the implications for future	 
congressional oversight. This testimony is based on recent GAO	 
reports examining these programs and related work by the	 
Department of Health and Human Services Office of Inspector	 
General and others.</abstract>
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<identifier type="preferred citation">GAO-07-481T</identifier>
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<note>Testimony</note>
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<subject>
 <topic>Beneficiaries</topic>
 <topic>Congressional oversight</topic>
 <topic>Medicaid</topic>
 <topic>Medicare</topic>
 <topic>Pharmaceutical industry</topic>
 <topic>Prescription drugs</topic>
 <topic>Prices and pricing</topic>
 <topic>Program abuses</topic>
 <topic>Program evaluation</topic>
 <topic>Executive agency oversight</topic>
 <topic>Transparency</topic>
 <topic>340B Drug Pricing Program</topic>
 <topic>Medicaid Drug Rebate Program</topic>
 <topic>Medicare Part D</topic>
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  <title>United States Statutes at Large</title>
  <partNumber>Volume 117 Page 2066</partNumber>
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 <identifier type="Statute citation">117 Stat. 2066</identifier>
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  <title>United States Statutes at Large</title>
  <partNumber>Volume 120 Page 4</partNumber>
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 <identifier type="Statute citation">120 Stat. 4</identifier>
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  <title>United States Public Law 173 (108th Congress)</title>
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 <identifier type="public law citation">Public Law 108-173</identifier>
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