97-6414. Notice Regarding Section 602 of the Veterans Health Care Act of 1992 Rebate Mechanism  

  • [Federal Register Volume 62, Number 50 (Friday, March 14, 1997)]
    [Notices]
    [Page 12219]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-6414]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    Health Resources and Services Administration
    
    
    Notice Regarding Section 602 of the Veterans Health Care Act of 
    1992 Rebate Mechanism
    
    AGENCY: Health Resources and Services Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: Section 602 of Public Law 102-585, the ``Veterans Health Care 
    Act of 1992,'' enacted section 340B of the Public Health Service (PHS) 
    Act, ``Limitation on Prices of Drugs Purchased by Covered Entities.'' 
    Section 340B provides that a manufacturer who sells covered outpatient 
    drugs to eligible entities must sign a pharmaceutical pricing agreement 
    with the Secretary of HHS in which the manufacturer agrees to charge a 
    price for covered outpatient drugs that will not exceed that amount 
    determined under a statutory formula.
        The purpose of this notice is to request comments on the proposal 
    of a rebate process for State AIDS Drug Assistance Programs (ADAPs) 
    receiving funds under Title XXVI of the PHS Act.
    
    DATES: The public is invited to submit comments on the proposed rebate 
    process by April 14, 1997. After consideration of comments submitted, 
    the Secretary will issue the final guideline.
    
    ADDRESS: Comments should be submitted to: Annette Byrne, R. Ph., M.S., 
    Director, Office of Drug Pricing Program, Bureau of Primary Health 
    Care, Health Resources and Services Administration, 4350 East-West 
    Highway, Bethesda, MD 20814, Phone (301) 594-4353; FAX (301) 594-4982.
    
    FOR FURTHER INFORMATION CONTACT: Robert Staley, R. Ph., Senior Program 
    Manager, Office of Drug Pricing Program, Bureau of Primary Health Care, 
    Health Resources and Services Administration, 4350 East-West Highway, 
    Bethesda, MD 20814, Phone (301) 594-4353; Fax (301) 594-4982.
    
    SUPPLEMENTARY INFORMATION: Section 340B requires manufacturers, as a 
    condition for the receipt of Medicaid matching funds with respect to 
    their covered outpatient drugs, to charge participating entities no 
    more than a ceiling price for such drugs. This price is determined by 
    reducing the average manufacturer price of the drug by a rebate 
    percentage. Entities eligible to access section 340B pricing (covered 
    entities) include certain PHS grantees (e.g., federally-qualified 
    health centers, certain family planning projects, AIDS assistance 
    programs, black lung clinics, hemophilia treatment centers, Native 
    Hawaiian health centers, and centers that treat sexually-transmitted 
    disease and/or tuberculosis) and certain disproportionate share 
    hospitals.
        Section 340B has no explicit language as to whether the required 
    reduction in price should be obtained by an initial reduction in the 
    purchase price (i.e., a discount system) or received as a required 
    reduction in cost rebated after purchase, dispensing, and payment are 
    completed (i.e., a rebate system). Section 340B(a)(1) of the PHS Act 
    provides that the amount to be paid to the manufacturers for covered 
    drugs takes ``into account any rebate or discount, as provided by the 
    Secretary * * * '' Further, section 340B does not specify whether 
    entities should receive the section 340B pricing ``through a point of 
    purchase discount, through a manufacturer rebate, or through some other 
    mechanism. A mechanism that is appropriate to one type of `covered 
    entity,' such as community health centers, may not be appropriate to 
    another type, such as State AIDS drug assistance programs * * * [T]he 
    Secretary of HHS * * * will use the mechanism that is the most 
    effective and most efficient * * * ''. H.R. Rep. No 102-384, 102d 
    Cong., 2d Sess., pt. 2, at 16 (1992).
        Initially, HRSA guidance for the section 340B program described 
    only a discount process. Covered entities generally preferred a 
    discount system, because they could negotiate lower prices and needed 
    less initial outlay of drug purchasing money.
        Although the discount system is functioning successfully for most 
    covered entities, most ADAPs have drug purchasing systems that have 
    prevented their participation in the section 340B discount program. The 
    use of a rebate mechanism (in addition to the discount mechanism) 
    should allow these groups to access section 340B pricing.
        The HRSA recognizes rebates obtained by the State ADAPs as a method 
    of accessing the section 340B discount price. The rebate for covered 
    outpatient drugs should be equal to or greater than the section 340B 
    discount at the time of purchase price. State ADAPs wishing technical 
    assistance in developing a rebate program should contact HRSA's Office 
    of Drug Pricing at (301) 594-4353 or (800) 628-6297.
        The HRSA is sensitive to concerns about diversion of covered drugs 
    to individuals who are not patients of the covered entities. Guidelines 
    have been issued to minimize this potential, and manufacturers have 
    available to them specified remedies if they believe diversion has 
    occurred. The HRSA believes that these guidelines and remedies will 
    apply fully to drugs purchased under a rebate procedure and that 
    instituting rebates will not increase the potential for diversion.
    
        Dated: March 10, 1997.
    Ciro V. Sumaya,
    Administrator.
    [FR Doc. 97-6414 Filed 3-13-97; 8:45 am]
    BILLING CODE 4160-15-P
    
    
    

Document Information

Published:
03/14/1997
Department:
Health Resources and Services Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
97-6414
Dates:
The public is invited to submit comments on the proposed rebate process by April 14, 1997. After consideration of comments submitted, the Secretary will issue the final guideline.
Pages:
12219-12219 (1 pages)
PDF File:
97-6414.pdf