[Federal Register Volume 60, Number 93 (Monday, May 15, 1995)]
[Notices]
[Pages 25919-25920]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-11930]



-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 95N-0109]


Animal Drug Export; Marbofloxacin

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing that 
Pfizer, Inc., has filed an application requesting approval for the 
export of a specific amount of the bulk form of the new drug substance 
marbofloxacin to France.

ADDRESSES: Relevant information on this application may be directed to 
the Dockets Management Branch (HFA-305), Food and Drug Administration, 
rm. 1-23, 12420 Parklawn Dr., Rockville, MD 20857, and to the contact 
person identified below. Any future inquiries concerning the export of 
animal drugs under the Drug Export Amendments Act of 1986 should also 
be directed to the contact person.

FOR FURTHER INFORMATION CONTACT: Gregory S. Gates, Center for 
Veterinary Medicine (HFV-114), Food and Drug Administration, 7500 
Standish Pl., Rockville, MD 20855, 301-594-1617.

SUPPLEMENTARY INFORMATION: The drug export provisions in section 802 of 
the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 382) 
provide that FDA may approve applications for the export of drugs that 
are not currently approved in the United States. Section 802(b)(3)(B) 
of the act sets forth the requirements that must be met in an 
application for approval. Section 802(b)(3)(C) of the act requires that 
the agency review the application within 30 days of its filing to 
determine whether the requirements of section 802(b)(3)(B) have been 
satisfied. Section 802 (b)(3)(A) of the act requires that the agency 
publish a notice in the Federal Register within 10 days of the filing 
of an application for export to facilitate public participation in its 
review of the application. To meet this requirement, the agency is 
providing notice that Pfizer, Inc., 235 East 42d St., New York, NY 
10017, has filed application number 6936 requesting approval for the 
export of a specific amount of the bulk form of the new drug substance 
marbofloxacin to France for further manufacture of the finished dosage 
form Marbocyl, 5 milligram Tablets (antimicrobial for treatment of dogs 
and cats). The tablets will then be shipped to the United Kingdom where 
they are approved for marketing. The application was received and filed 
in the Center for Veterinary Medicine on April 24, 1995, which shall be 
considered the filing date for purposes of the act.
    Interested persons may submit relevant information on the 
application to the Dockets Management Branch (address above) in two 
copies (except that individuals may submit single copies) and 
identified with the docket number found in brackets in the heading of 
this document. These submissions may be seen in the Dockets Management 
Branch between 9 a.m. and 4 p.m., Monday through Friday.
    The agency encourages any person who submits relevant information 
on the application to do so by May 25, 1995, and to provide an 
additional copy of the submission directly to the contact person 
identified above, to facilitate consideration of the information during 
the 30-day review period.
    This notice is issued under the Federal Food, Drug, and Cosmetic 
Act (sec. 802 (21 U.S.C. 382)) and under authority delegated to the 
Commissioner of Food and Drugs (21 CFR 5.10) and redelegated to the 
Center for Veterinary Medicine D(21 CFR 5.44).

    [[Page 25920]] Dated: May 5, 1995.
Robert C. Livingston,
Director, Office of New Animal Drug Evaluation, Center for Veterinary 
Medicine.
[FR Doc. 95-11930 Filed 5-12-95; 8:45 am]
BILLING CODE 4160-01-F