Medical Device User Fee Rates for Fiscal Year 2006; Delay in Publication, 44105 [05-15157]

Download as PDF Federal Register / Vol. 70, No. 146 / Monday, August 1, 2005 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2000N–1571] Enrofloxacin for Poultry; Final Decision on Withdrawal of New Animal Drug Application Following Formal Evidentiary Public Hearing; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of the final decision setting forth the findings of fact and conclusions of law on the issues addressed in a formal evidentiary public hearing to determine whether FDA should withdraw approval of the new animal drug application (NADA) for use of enrofloxacin in poultry. Once this final decision becomes effective on September 12, 2005, this drug may no longer be distributed or administered for this use in the United States, nor may it be exported except as allowed by law. Elsewhere in this issue of the Federal Register, a final rule removing the applicable regulations is published. ADDRESSES: The transcript of the hearing, evidence submitted, and the final decision, may be seen in the Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, rm.1061, Rockville, MD 20852. See the SUPPLEMENTARY INFORMATION section for electronic access to these documents. FOR FURTHER INFORMATION CONTACT: Erik P. Mettler, Office of Policy (HF–11), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827–3360. SUPPLEMENTARY INFORMATION: I. Background On October 31, 2000, FDA’s Center for Veterinary Medicine (CVM) proposed to withdraw the approval of the NADA 140–828 for the use in chickens and turkeys of enrofloxacin, an antimicrobial drug belonging to a class of drugs known as fluoroquinolones (65 FR 64954, October 31, 2000). On November 29, 2000, Bayer Corp. (Bayer), the sponsor of enrofloxacin (sold under the trade name Baytril 3.23% Concentrate Antimicrobial Solution), requested a hearing on the proposed withdrawal. On February 20, 2002, FDA’s then Acting Principal Deputy Commissioner published a notice of hearing granting Bayer’s request and identifying the factual issues that would VerDate jul<14>2003 14:01 Jul 29, 2005 Jkt 205001 be the subject of the evidentiary hearing (67 FR 7700, February 20, 2002). On March 21, 2002, the Animal Health Institute submitted a notice of participation under 21 CFR 12.45. Oral hearing for the purposes of crossexamination of witnesses was held at FDA from April 28 through May 7, 2003. On March 16, 2004, an FDA Administrative Law Judge (ALJ) issued an initial decision under 21 CFR 12.120. The ALJ determined that enrofloxacin had not been ‘‘shown to be safe under the conditions of use upon the basis of which the application was approved,’’ as required under section 512(e)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 360b(e)(1)(B)) and ordered that the approval of the NADA for Baytril be withdrawn. Bayer and CVM each filed exceptions to the initial decision on May 17, 2004. After reviewing the evidence in the administrative record and the exceptions to the initial decision, I have issued a final decision withdrawing the approval of the NADA for use of enrofloxacin in poultry, for the reasons described more fully in the final decision that is the subject of this notice. In addition, elsewhere in this issue of the Federal Register, a final rule removing the applicable regulations is published. II. Electronic Access Persons with access to the Internet may obtain the final decision at www.fda.gov/oc/antimicrobial/ baytril.pdf. The final decision as well as documents cited in the decision are available for inspection by means of writing to, or visiting, the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All other documents related to this docket also are available for inspection, unless considered confidential. Dated: July 27, 2005. Lester M. Crawford, Commissioner of Food and Drugs. [FR Doc. 05–15224 Filed 7–28–05; 2:31 pm] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Medical Device User Fee Rates for Fiscal Year 2006; Delay in Publication AGENCY: SUMMARY: The Food and Drug Administration (FDA) is announcing a delay in the publication of the fee rates and payment procedures for medical device user fees for fiscal year (FY) 2006. FOR FURTHER INFORMATION CONTACT: For further information on MDUFMA: Visit FDA’s Internet site at https:// www.fda.gov/oc/mdufma. For questions relating to this notice: Frank Claunts, Office of Management (HFA–20), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301– 827–4427. The Federal Food, Drug, and Cosmetic Act (the act), as amended by the Medical Device User Fee and Modernization Act of 2002 (MDUFMA), authorizes FDA to collect user fees for certain medical device applications in FY 2006 and FY 2007 only if certain conditions are met. Section 738 of the act (21 U.S.C. 379j) establishes fees for certain medical device applications and supplements. However, MDUFMA specifies that for FY 2006 fees may not be assessed if the total amounts appropriated for FY 2003 through FY 2005 for FDA’s device and radiological health program are less than levels specified in MDUFMA (21 U.S.C. 379j(g)(1)(C)). Appropriations for FY 2003 through FY 2005 for FDA’s device and radiological health program are below the amount specified in MDUFMA. Because of this, FDA is unable to assess or collect medical device user fees in FY 2006 unless additional legislation is enacted to modify those conditions (minimum appropriation levels for FY 2003 through FY 2005). Accordingly, FDA is not publishing the fee rates for FY 2006 at this time. If the required legislation is enacted, within 2 weeks of the date of enactment FDA will make available the fee rates for all applications and supplements submitted on or after October 1, 2005, and through September 30, 2006. SUPPLEMENTARY INFORMATION: Dated: July 22, 2005. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. 05–15157 Filed 7–29–05; 8:45 am] BILLING CODE 4160–01–S Food and Drug Administration, HHS. ACTION: PO 00000 Notice. Frm 00023 Fmt 4703 Sfmt 4703 44105 E:\FR\FM\01AUN1.SGM 01AUN1

Agencies

[Federal Register Volume 70, Number 146 (Monday, August 1, 2005)]
[Notices]
[Page 44105]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-15157]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration


Medical Device User Fee Rates for Fiscal Year 2006; Delay in 
Publication

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing a delay 
in the publication of the fee rates and payment procedures for medical 
device user fees for fiscal year (FY) 2006.

FOR FURTHER INFORMATION CONTACT:
    For further information on MDUFMA: Visit FDA's Internet site at 
https://www.fda.gov/oc/mdufma.
    For questions relating to this notice: Frank Claunts, Office of 
Management (HFA-20), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-4427.

SUPPLEMENTARY INFORMATION: The Federal Food, Drug, and Cosmetic Act 
(the act), as amended by the Medical Device User Fee and Modernization 
Act of 2002 (MDUFMA), authorizes FDA to collect user fees for certain 
medical device applications in FY 2006 and FY 2007 only if certain 
conditions are met. Section 738 of the act (21 U.S.C. 379j) establishes 
fees for certain medical device applications and supplements. However, 
MDUFMA specifies that for FY 2006 fees may not be assessed if the total 
amounts appropriated for FY 2003 through FY 2005 for FDA's device and 
radiological health program are less than levels specified in MDUFMA 
(21 U.S.C. 379j(g)(1)(C)). Appropriations for FY 2003 through FY 2005 
for FDA's device and radiological health program are below the amount 
specified in MDUFMA. Because of this, FDA is unable to assess or 
collect medical device user fees in FY 2006 unless additional 
legislation is enacted to modify those conditions (minimum 
appropriation levels for FY 2003 through FY 2005). Accordingly, FDA is 
not publishing the fee rates for FY 2006 at this time. If the required 
legislation is enacted, within 2 weeks of the date of enactment FDA 
will make available the fee rates for all applications and supplements 
submitted on or after October 1, 2005, and through September 30, 2006.

    Dated: July 22, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05-15157 Filed 7-29-05; 8:45 am]
BILLING CODE 4160-01-S

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