[Federal Register Volume 59, Number 53 (Friday, March 18, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-6290]


[[Page Unknown]]

[Federal Register: March 18, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 94N-0084]

 

Drug Export; Humatrope [Somatropin (rDNA Origin) for 
Injection] in Glass Cartridges: 18, 36, and 72 International Units Per 
Cartridge [Equivalent to 6.66, 13.32, and 26.64 Milligrams Per 
Cartridge]

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 has filed an application requesting 
approval for the export of the human drug Humatrope 
[Somatropin (rDNA origin) for injection] in glass cartridges: 18, 36, 
and 72 International Units (IU) per cartridge [equivalent to 6.66, 
13.32, and 26.64 milligrams (mg) per cartridge] 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, Division of Drug 
Labeling Compliance (HFD-313), Center for Drug Evaluation and Research, 
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 approval for the export of the human 
drug Humatrope [Somatropin (rDNA origin) for injection] in 
glass cartridges: 18, 36, and 72 IU per cartridge [equivalent to 6.66, 
13.32, and 26.64 mg per cartridge] for use in humans for the treatment 
of growth hormone deficiency or short stature associated with Turner's 
syndrome. The application was received and filed in the Center for Drug 
Evaluation and Research on December 23, 1993, which shall be considered 
the filing date for purposes of the act. The firm has an approved new 
drug application to market Humatrope at 5 mg/glass vial.
    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 March 28, 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: March 8, 1994.
 Raymond E. Hamilton,
 Acting Director, Office of Compliance, Center for Drug Evaluation and 
Research.
[FR Doc. 94-6290 Filed 3-17-94; 8:45 am]
BILLING CODE 4160-01-F