![]() |
![]() |
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA
![]()
Meeting Cancelled
See Meeting
Cancellation Notice
| Center | Date | Time | Location |
|---|---|---|---|
| CDER | May 10, 2004 | 8:30 a.m. - 5:30 p.m. | Center for Drug
Evaluation and Research |
Agenda:
The committee will discuss new drug application (NDA) 21-678, gatifloxacin (proposed
tradename, TEQUIN) for oral suspension, Bristol-Myers Squibb, studied in the
treatment of recurrent bacterial otitis media and treatment failures of acute
bacterial otitis media in pediatric patients.
Background material and meeting information will become available no later than the day before the meeting (Simply select the appropriate 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 by April 30, 2004. Oral presentations from the public will be
scheduled between approximately 1:30 p.m. and 2:30 p.m. Time allotted for each
presentation may be limited. Those desiring to make formal oral presentations
should notify the contact person before April 30, 2004, 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. Persons attending FDA's advisory
committee meetings are advised that the 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 Tara Turner at least 7 days in advance of the meeting.
Contact Person:
Tara P. Turner, Center for Drug Evaluation and Research (HFD-21), Food and Drug
Administration, 5600 Fishers Lane (for express delivery, 5630 Fishers Lane,
Rm. 1093), Rockville, MD 20857, 301-827-7001, e-mail: TurnerT@cder.fda.gov,
or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in
the Washington, DC area), code 3014512530. Please call the Information Line
for up-to-date information on this meeting.
[ Full FR Notice ]
![]()