[Federal Register Volume 59, Number 203 (Friday, October 21, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-26077]


[[Page Unknown]]

[Federal Register: October 21, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 94N-0374]

 

Drug Export; Gemzar (Gemcitabine Hydrochloride) Bulk 
Drug or Glass Vials: 200 MG or 1 G (Free Base) Per Vial

AGENCY: Food and Drug Administration, HHS.

ACTION:  Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that 
Lilly Research Laboratories, A Division of Eli Lilly and Co., has filed 
an application requesting conditional approval for the export of the 
human drug Gemzar (gemcitabine hydrochloride) bulk drug or 
glass vials: 200 mg or 1 g (free base) per vial 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 
human drugs under the Drug Export Amendments Act of 1986 should also be 
directed to the contact person.

FOR FURTHER INFORMATION CONTACT: James E. Hamilton, Center for Drug 
Evaluation and Research (HFD-313), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-594-2073.
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 Lilly Research Laboratories, A Division of Eli 
Lilly and Co., Lilly Corporate Center, Indianapolis, IN 46285, has 
filed an application requesting conditional approval for the export of 
the human drug Gemzar (gemcitabine hydrochloride) bulk drug 
or glass vials: 200 mg or 1 g (free base) per vial to France. 
Gemzar is indicated for the treatment of patients with 
locally advanced or metastatic nonsmall cell lung cancer.
    The application was received and filed in the Center for Drug 
Evaluation and Research on August 18, 1994, 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 October 31, 1994, 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 Drug Evaluation and Research (21 CFR 5.44).

    Dated: September 29, 1994.
David B. Barr,
Deputy Director, Office of Compliance, Center for Drug Evaluation and 
Research
[FR Doc. 94-26077 Filed 10-20-94; 8:45 am]
BILLING CODE 4160-01-F