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<bill bill-stage="Introduced-in-House" dms-id="H141FAC1DFAE747FFA640243931F998BF" public-private="public" bill-type="olc"> 
<metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
<dublinCore>
<dc:title>109 HR 5102 IH: Medicare Drug Formulary Protection Act</dc:title>
<dc:publisher>U.S. House of Representatives</dc:publisher>
<dc:date>2006-04-05</dc:date>
<dc:format>text/xml</dc:format>
<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
</dublinCore>
</metadata>
<form> 
<distribution-code display="yes">I</distribution-code> 
<congress>109th CONGRESS</congress>
<session>2d Session</session>
<legis-num>H. R. 5102</legis-num> 
<current-chamber>IN THE HOUSE OF REPRESENTATIVES</current-chamber> 
<action> 
<action-date date="20060405">April 5, 2006</action-date> 
<action-desc><sponsor name-id="B000287">Mr. Becerra</sponsor> (for himself, <cosponsor name-id="D000191">Mr. DeFazio</cosponsor>, <cosponsor name-id="S001158">Mr. Salazar</cosponsor>, <cosponsor name-id="H001034">Mr. Honda</cosponsor>, <cosponsor name-id="J000070">Mr. Jefferson</cosponsor>, <cosponsor name-id="K000113">Mr. Kennedy of Rhode Island</cosponsor>, <cosponsor name-id="B000657">Mr. Boucher</cosponsor>, <cosponsor name-id="W000314">Mr. Wexler</cosponsor>, <cosponsor name-id="C001050">Mr. Cardoza</cosponsor>, <cosponsor name-id="M000312">Mr. McGovern</cosponsor>, <cosponsor name-id="M000844">Mr. Mollohan</cosponsor>, <cosponsor name-id="G000410">Mr. Gene Green of Texas</cosponsor>, <cosponsor name-id="G000551">Mr. Grijalva</cosponsor>, <cosponsor name-id="R000053">Mr. Rangel</cosponsor>, <cosponsor name-id="S000810">Mr. Stark</cosponsor>, <cosponsor name-id="C000714">Mr. Conyers</cosponsor>, <cosponsor name-id="M000404">Mr. McDermott</cosponsor>, <cosponsor name-id="H001037">Ms. Herseth</cosponsor>, <cosponsor name-id="H000627">Mr. Hinchey</cosponsor>, <cosponsor name-id="B000944">Mr. Brown of Ohio</cosponsor>, <cosponsor name-id="R000170">Mr. Reyes</cosponsor>, <cosponsor name-id="R000576">Mr. Ruppersberger</cosponsor>, <cosponsor name-id="L000557">Mr. Larson of Connecticut</cosponsor>, <cosponsor name-id="M000590">Mr. McNulty</cosponsor>, <cosponsor name-id="M001163">Ms. Matsui</cosponsor>, <cosponsor name-id="C000794">Mr. Costello</cosponsor>, <cosponsor name-id="M000087">Mrs. Maloney</cosponsor>, <cosponsor name-id="M001146">Mr. Marshall</cosponsor>, <cosponsor name-id="L000263">Mr. Levin</cosponsor>, <cosponsor name-id="N000147">Ms. Norton</cosponsor>, <cosponsor name-id="I000026">Mr. Inslee</cosponsor>, <cosponsor name-id="L000562">Mr. Lynch</cosponsor>, <cosponsor name-id="D000210">Mr. Delahunt</cosponsor>, <cosponsor name-id="O000159">Mr. Owens</cosponsor>, <cosponsor name-id="O000107">Mr. Ortiz</cosponsor>, <cosponsor name-id="S001145">Ms. Schakowsky</cosponsor>, <cosponsor name-id="N000179">Mrs. Napolitano</cosponsor>, <cosponsor name-id="R000577">Mr. Ryan of Ohio</cosponsor>, <cosponsor name-id="D000482">Mr. Doyle</cosponsor>, <cosponsor name-id="P000422">Mr. Pomeroy</cosponsor>, <cosponsor name-id="S000185">Mr. Scott of Virginia</cosponsor>, <cosponsor name-id="B001234">Mr. Baca</cosponsor>, <cosponsor name-id="S000033">Mr. Sanders</cosponsor>, <cosponsor name-id="C000984">Mr. Cummings</cosponsor>, <cosponsor name-id="O000006">Mr. Oberstar</cosponsor>, <cosponsor name-id="P000149">Mr. Payne</cosponsor>, <cosponsor name-id="G000544">Mr. Gonzalez</cosponsor>, <cosponsor name-id="E000287">Mr. Emanuel</cosponsor>, <cosponsor name-id="L000090">Mr. Lantos</cosponsor>, <cosponsor name-id="D000399">Mr. Doggett</cosponsor>, <cosponsor name-id="W001159">Ms. Wasserman Schultz</cosponsor>, <cosponsor name-id="B001227">Mr. Brady of Pennsylvania</cosponsor>, <cosponsor name-id="C001036">Mrs. Capps</cosponsor>, and <cosponsor name-id="M001143">Ms. McCollum of Minnesota</cosponsor>) introduced the following bill; which was referred to the <committee-name committee-id="HIF00">Committee on Energy and Commerce</committee-name>, and in addition to the Committee on <committee-name committee-id="HWM00">Ways and Means</committee-name>, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned</action-desc>
</action> 
<legis-type>A BILL</legis-type> 
<official-title>To amend title XVIII of the Social Security Act to prohibit removal of covered part D drugs from a prescription drug plan formulary during the plan year once an individual has enrolled in the plan.</official-title> 
</form> 
<legis-body id="H93CBE60EDD7D4F619E618505745F23BC" style="OLC"> 
<section id="H92F032FAC1ED43EC8C6D9FE2194B7D14" section-type="section-one" display-inline="no-display-inline"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Medicare Drug Formulary Protection Act</short-title></quote>.</text></section> 
<section commented="no" display-inline="no-display-inline" id="H9C47E1D5D62C4A18952600ED22AA5469"><enum>2.</enum><header>Removal of covered part D drugs from the prescription drug plan formulary</header> 
<subsection commented="no" display-inline="no-display-inline" id="HD6D7BAA1FC2A4E59B2002FE3004BF8F9"><enum>(a)</enum><header>Limitation on removal or change of covered part D drugs from the prescription drug plan formulary</header><text display-inline="yes-display-inline">Section 1860D–4(b)(3)(E) of the Social Security Act (<external-xref legal-doc="usc" parsable-cite="usc/42/1395w-104">42 U.S.C. 1395w–104(b)(3)(E)</external-xref>) is amended to read as follows:</text> 
<quoted-block display-inline="no-display-inline" id="H6C30CA157C754AFB95E6BA3C395662F9" style="OLC"> 
<subparagraph commented="no" display-inline="no-display-inline" id="HB5C9F38CFAD44CCCA49C310409866EA1"><enum>(E)</enum><header>Removing a drug from formulary or imposing a restriction or limitation on coverage</header> 
<clause commented="no" display-inline="no-display-inline" id="H4A5CCF41B3554B9C9F085505F154CE33"><enum>(i)</enum><header>Limitation on removal, limitation, or restriction</header> 
<subclause commented="no" display-inline="no-display-inline" id="HC620A135EEDD4D54B66082A281622857"><enum>(I)</enum><header>In general</header><text>Subject to subclause (II) and clause (ii), beginning with 2006, the PDP sponsor of a prescription drug plan may not remove a covered part D drug from the plan formulary or impose a restriction or limitation on the coverage of such a drug (such as through the application of a preferred status, usage restriction, step therapy, prior authorization, or quantity limitation) other than at the beginning of each plan year except as the Secretary may permit to take into account new therapeutic uses and newly covered part D drugs.</text></subclause> 
<subclause commented="no" display-inline="no-display-inline" id="H9DF941A7A4034E4E954D5DEF649F6E14"><enum>(II)</enum><header>Special rule for newly enrolled individuals</header><text display-inline="yes-display-inline">Subject to clause (ii), in the case of an individual who enrolls in a prescription drug plan on or after the date of the enactment of the <short-title>Medicare Drug Formulary Protection Act</short-title>, the PDP sponsor of such plan may not remove a covered part D drug from the plan formulary or impose a restriction or limitation on the coverage of such a drug (such as through the application of a preferred status, usage restriction, step therapy, prior authorization, or quantity limitation) during the period beginning on the date of such enrollment and ending on December 31 of the immediately succeeding plan year except as the Secretary may permit to take into account new therapeutic uses and newly covered part D drugs.</text></subclause></clause> 
<clause commented="no" display-inline="no-display-inline" id="HC4E14429CB1E49E3B8C3AE34C785E690"><enum>(ii)</enum><header>Exceptions to limitation on removal</header><text>Clause (i) shall not apply with respect to a covered part D drug that—</text> 
<subclause commented="no" display-inline="no-display-inline" id="HB9979E3BC4434D8B8B0123BCE92D9FE3"><enum>(I)</enum><text>is a brand name drug for which there is a generic drug approved under section 505(j) of the Food and Drug Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/355">21 U.S.C. 355(j)</external-xref>) that is placed on the market during the period in which there are limitations on removal or change in the formulary under subclause (I) or (II) of clause (i) if such generic drug is included in the formulary without any restriction or limitation placed on the coverage of such generic drug other than a restriction or limitation that would be placed on the coverage of the brand name drug during such period without the application of this subclause;</text></subclause> 
<subclause commented="no" display-inline="no-display-inline" id="H5AC8640FC8914B5C0089D0EE4DB58CD9"><enum>(II)</enum><text>is a brand name drug that goes off-patent during such period;</text></subclause> 
<subclause commented="no" display-inline="no-display-inline" id="H131F4A74EB0E4D378683542371E91262"><enum>(III)</enum><text>is a drug for which the Commissioner of Food and Drugs issues a clinical warning that imposes a restriction or limitation on the drug during such period;</text></subclause> 
<subclause commented="no" display-inline="no-display-inline" id="H28322C5A1C134AFA8F4D029FB08DF4C7"><enum>(IV)</enum><text>has been determined to be ineffective during such period;</text></subclause> 
<subclause id="HA309EB66C48147C5BB1CA8002791B931"><enum>(V)</enum><text display-inline="yes-display-inline">is a drug that the appropriate pharmacy and therapeutic committee determines, based on evidence from peer-reviewed research, to be unsafe or ineffective during such period; or</text></subclause> 
<subclause id="H9C6BA18DCF9F43DC00EAB8E2964DD8D5"><enum>(VI)</enum><text>is any other drug that satisfies any other requirement determined appropriate by the Secretary. </text></subclause></clause> 
<clause commented="no" display-inline="no-display-inline" id="HB4C4D580C7224404B301C2BE20E698A9"><enum>(iii)</enum><header>Notice of removal under application of exception to limitation</header><text>The PDP sponsor of a prescription drug plan shall provide appropriate notice (such as under subsection (a)(3)) of any removal or change under clause (ii) to the Secretary, affected enrollees, physicians, pharmacies, and pharmacists.</text></clause></subparagraph><after-quoted-block>.</after-quoted-block></quoted-block></subsection> 
<subsection id="H27BEAC53669545ADBF1CAA006D9CF800"><enum>(b)</enum><header>Notice for change in formulary and other restrictions or limitations on coverage</header> 
<paragraph id="HE5BCFDA10E03437B91E266E71B90E781"><enum>(1)</enum><header>In general</header><text>Section 1860D–4(a) of such Act (<external-xref legal-doc="usc" parsable-cite="usc/42/1395w-104">42 U.S.C. 1395w–104(a)</external-xref>) is amended by adding at the end the following new paragraph:</text> 
<quoted-block display-inline="no-display-inline" id="H6F6074A33BA34847007BB3CD48CB523E" style="OLC"> 
<paragraph id="H1EB09DC5694D41F2B934EE0057C16B9B"><enum>(5)</enum><header>Annual notice of changes in formulary and other restrictions or limitations on coverage</header><text>Each PDP sponsor offering a prescription drug plan shall furnish to each enrollee at the time of each annual coordinated election period (referred to in section 1860D–1(b)(1)(B)(iii)) for a plan year a notice of any changes in the formulary or other restrictions or limitations on coverage of a covered part D drug under the plan that will take effect for the plan year.</text></paragraph><after-quoted-block>.</after-quoted-block></quoted-block></paragraph> 
<paragraph commented="no" display-inline="no-display-inline" id="H886E725A125744A5BC99E1EC4F43FE5"><enum>(2)</enum><header>Effective date</header><text>The amendment made by paragraph (1) shall apply to annual coordinated election periods beginning after the date of the enactment of this Act.</text></paragraph></subsection></section> 
</legis-body> 
</bill> 

