Drug Safety and Risk Management Advisory Committee; Notice of Meeting, 23782-23783 [2010-10384]

Agencies

• Food and Drug Administration
• DEPARTMENT OF HEALTH AND HUMAN SERVICES

[Federal Register Volume 75, Number 85 (Tuesday, May 4, 2010)]
[Notices]
[Pages 23782-23783]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-10384]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2010-N-0001]


Drug Safety and Risk Management Advisory Committee; Notice of 
Meeting

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Notice.

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    This notice announces a forthcoming meeting of a public advisory 
committee of the Food and Drug Administration (FDA). The meeting will 
be open to the public.
    Name of Committee: Drug Safety and Risk Management Advisory 
Committee.
    General Function of the Committee: To provide advice and 
recommendations to the agency on FDA's regulatory issues.
    Date and Time: The meeting will be held on September 14, 2010, from 
8 a.m. to 5 p.m.
    Location: The Marriott Inn and Conference Center, University of 
Maryland and University College (UMUC), The Ballrooms, 3501 University 
Blvd. East, Adelphi, MD. The conference center telephone number is 301-
985-7300.
    Contact Person: Elaine Ferguson, e-mail: 
elaine.ferguson@fda.hhs.gov (contact information through June 8, 2010, 
Elaine Ferguson c/o Melanie Whelan, Food and Drug Administration, 10903 
New Hampshire Ave., WO51-6100, Silver Spring, MD 20993-0002, telephone: 
301-827-7001, FAX: 301-847-8742), (contact information beginning June 
9, 2010: Elaine Ferguson c/o Christine Shipe, Food and Drug 
Administration, 10903 New Hampshire Ave., WO31-2419, Silver Spring, MD 
20993-0002, telephone: 301-0796-9001, FAX: 301-847-8532), or FDA 
Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in 
the Washington, DC area), code 3014512535. Please call the Information 
Line for up-to-date information on this meeting. A notice in the 
Federal Register about last minute modifications that impact a 
previously announced advisory committee meeting cannot always be 
published quickly enough to provide timely notice. Therefore, you 
should always check the agency's Web site and call the appropriate 
advisory committee hot line/phone line to learn about possible 
modifications before coming to the meeting.
    Agenda: On September 14, 2010, the committee will discuss the abuse 
potential of the drug dextromethorphan and the public health benefits 
and risks of dextromethorphan use as a cough suppressant in 
prescription and nonprescription drug products. The Department of 
Health and Human Services received a request from the Drug Enforcement 
Administration for a scientific and medical evaluation and scheduling 
recommendation for dextromethorphan in response to the increased 
incidence of abuse, especially among adolescents.
    FDA intends to make background material available to the public no 
later than 2 business days before the meeting. If FDA is unable to post 
the background material on its Web site prior to the meeting, the 
background material will be made publicly available at the location of 
the advisory committee meeting, and the background material will be 
posted on FDA's Web site after the meeting. Background material is 
available at https://www.fda.gov/AdvisoryCommittees/Calendar/default.htm. Scroll down to the appropriate advisory committee link.
    Procedure: Interested persons may present data, information, or 
views, orally or in writing, on issues pending before the committee. 
Written submissions may be made to the contact person on or before 
August 30, 2010. Oral presentations from the public will be scheduled 
between approximately 1 p.m. to 2 p.m. Those desiring to make formal 
oral presentations should notify the contact person and submit a brief 
statement of the general nature of the evidence or arguments they wish 
to present, the names and addresses of proposed participants, and an 
indication of the approximate time requested to make their presentation 
on or before August 20, 2010. Time allotted for each presentation may 
be limited. If the number of registrants requesting to speak is greater 
than can be reasonably accommodated during the scheduled open public 
hearing session, FDA may conduct a lottery to determine the speakers 
for the scheduled open public hearing session. The contact person will 
notify interested persons regarding their request to speak by August 
23, 2010.
    Persons attending FDA's advisory committee meetings are advised 
that the

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agency is not responsible for providing access to electrical outlets.
    FDA welcomes the attendance of the public at its advisory committee 
meetings and will make every effort to accommodate persons with 
physical disabilities or special needs. If you require special 
accommodations due to a disability, please contact Elaine Ferguson at 
least 7 days in advance of the meeting.
    FDA is committed to the orderly conduct of its advisory committee 
meetings. Please visit our Web site at https://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm111462.htm for procedures 
on public conduct during advisory committee meetings.
    Notice of this meeting is given under the Federal Advisory 
Committee Act (5 U.S.C. app. 2).

    Dated: April 27, 2010.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
[FR Doc. 2010-10384 Filed 5-3-10; 8:45 am]
BILLING CODE 4160-01-S