New Animal Drugs for Use in Animal Feed; Pyrantel; Technical Amendment, 15661 [E8-5928]

Download as PDF Federal Register / Vol. 73, No. 58 / Tuesday, March 25, 2008 / Rules and Regulations Dated: March 13, 2008. Todd A. Stevenson, Secretary, Consumer Product Safety Commission. Note: The following appendix will not appear in the Code of Federal Regulations. Appendix—List of Relevant Documents (The following documents are available from the Commission’s Office of the Secretary, Consumer Product Safety Commission, Room 502, 4330 East West Highway, Bethesda, Maryland 20814–4408; telephone (301) 504– 7923 or from the Commission’s Web site (http://www.cpsc.gov/library/foia/foia.html )). 1. Briefing memorandum from Robert J. Howell, Acting Assistant Executive Director, EXHR and Patricia K. Adair, Project Manager, Directorate for Engineering Sciences, to the Commission, ‘‘Draft Final Amendments to the Standard for the Flammability of Clothing Textiles, 16 CFR Part 1610,’’ January 11, 2008. 2. Memorandum from David Miller, EPHA, Directorate for Epidemiology, to Patricia K. Adair, Project Manager, ‘‘General Wearing Apparel Fires—Fatalities and Emergency Department Treated Injuries,’’ December 27, 2007. 3. Memorandum from Dale R. Ray, Directorate for Economic Analysis, to Patricia K. Adair, Project Manager, ‘‘Final Regulatory Analyses—Clothing Textiles Standard Amendment,’’ August 6, 2007. 4. Memorandum from Gail Stafford and Weiying Tao, Directorate for Laboratory Sciences, to Patricia K. Adair, Project Manager, ‘‘Response to Comments Received on Notice of Proposed Rulemaking (NPR) for Updating the Standard for the Flammability of Clothing Textiles,’’ October 22, 2007. 5. Memorandum from John R. Murphy, Division of Mechanical Engineering, to Patricia K. Adair, Project Manager, ‘‘Response to Comments Received as a Result of the Notice of Proposed Rulemaking (NPR) for Updating the Standard for the Flammability of Clothing Textiles,’’ November 16, 2007. 6. Memorandum from Martha A. Kosh, Office of the Secretary, to ES, ‘‘Proposed Changes to Textile Flammability Standard Comments,’’ May 15, 2007. [FR Doc. E8–5569 Filed 3–24–08; 8:45 am] SUMMARY: The Food and Drug Administration (FDA) is amending its animal drug regulations to correct an inadvertent omission in the list of concentrations of pyrantel tartrate Type A medicated articles approved for use by Phibro Animal Health. This action is being taken to improve the accuracy of the animal drug regulations. DATES: This rule is effective March 25, 2008. George K. Haibel, Center for Veterinary Medicine (HFV–6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240–276–9019, email: george.haibel@fda.hhs.gov. FDA is amending the animal drug regulations in 21 CFR 558.485 to correct an inadvertent omission in the list of concentrations of pyrantel tartrate Type A medicated articles approved for use by Phibro Animal Health. This action is being taken to improve the accuracy of the animal drug regulations. This rule does not meet the definition of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because it is a rule of ‘‘particular applicability.’’ Therefore, it is not subject to the congressional review requirements in 5 U.S.C. 801–808. SUPPLEMENTARY INFORMATION: List of Subjects in 21 CFR Part 558 Animal drugs, Animal feeds. Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, 21 CFR part 558 is amended as follows: I PART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS 1. The authority citation for 21 CFR part 558 continues to read as follows: I Authority: 21 U.S.C. 360b, 371. § 558.485 DEPARTMENT OF HEALTH AND HUMAN SERVICES 2. In § 558.485, in paragraph (b)(1), add ‘‘48,’’ in numerical sequence. 21 CFR Part 558 pwalker on PROD1PC71 with RULES New Animal Drugs for Use in Animal Feed; Pyrantel; Technical Amendment AGENCY: [Amended] I Food and Drug Administration Dated: March 12, 2008. Bernadette Dunham, Director, Center for Veterinary Medicine. [FR Doc. E8–5928 Filed 3–24–08; 8:45 am] BILLING CODE 4160–01–S Final rule; technical amendment. Jkt 214001 PO 00000 23 CFR Part 661 [FHWA Docket No. FHWA–2007–27536] RIN 2125–AF20 Indian Reservation Road Bridge Program Federal Highway Administration (FHWA), DOT. ACTION: Final rule. SUMMARY: Section 1119 of the Safe, Accountable, Flexible, Efficient Transportation Equity Act: A Legacy for Users (SAFETEA–LU) (Pub. L. 109–59, 119 Stat. 1144) makes significant changes to the Indian Reservation Road Bridge Program (IRRBP). In addition, it authorizes $14 million of IRRBP funds per year for the replacement or rehabilitation of structurally deficient or functionally obsolete Indian Reservation Road (IRR) bridges. This final rule amends the existing IRRBP by establishing new policies and provisions. Also, in this final rule, preliminary engineering (PE) is now an eligible activity. DATES: Effective April 24, 2008. FOR FURTHER INFORMATION CONTACT: Mr. Robert Sparrow, Federal Lands Highway, HFPD–9, (202) 366–9483; or Ms. Vivian Philbin, Federal Lands Highway Counsel, HFFC–16, (720) 963– 3445; Federal Highway Administration, 1200 New Jersey Avenue, SE., Washington, DC 20590. Office hours are from 7:45 a.m. to 4:15 p.m., e.t., Monday through Friday, except Federal holidays. SUPPLEMENTARY INFORMATION: Electronic Access and Filing Internet users may access this document, the notice of proposed rulemaking (NPRM), and all comments received by the DOT by accessing the Federal eRulemaking portal at: http:// www.regulations.gov. It is available 24 hours each day, 365 days each year. Electronic submission and retrieval help and guidelines are available under the help section of the Web site. An electronic copy of this document may also be downloaded by accessing the Office of the Federal Register’s home page at: http://www.archives.gov or the Government Printing Office’s Web page at http://www.gpoaccess.gov/nara. The Transportation Equity Act for the 21st Century (TEA–21) (Pub. L. 105– 178, 112 Stat. 107), established the IRRBP, codified at 23 U.S.C. HHS. ACTION: 17:24 Mar 24, 2008 Federal Highway Administration Background Food and Drug Administration, VerDate Aug<31>2005 DEPARTMENT OF TRANSPORTATION AGENCY: FOR FURTHER INFORMATION CONTACT: BILLING CODE 6355–01–P 15661 Frm 00027 Fmt 4700 Sfmt 4700 E:\FR\FM\25MRR1.SGM 25MRR1

Agencies

[Federal Register Volume 73, Number 58 (Tuesday, March 25, 2008)]
[Rules and Regulations]
[Page 15661]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-5928]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 558


New Animal Drugs for Use in Animal Feed; Pyrantel; Technical 
Amendment

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; technical amendment.

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

SUMMARY: The Food and Drug Administration (FDA) is amending its animal 
drug regulations to correct an inadvertent omission in the list of 
concentrations of pyrantel tartrate Type A medicated articles approved 
for use by Phibro Animal Health. This action is being taken to improve 
the accuracy of the animal drug regulations.

DATES: This rule is effective March 25, 2008.

FOR FURTHER INFORMATION CONTACT: George K. Haibel, Center for 
Veterinary Medicine (HFV-6), Food and Drug Administration, 7519 
Standish Pl., Rockville, MD 20855, 240-276-9019, e-mail: 
george.haibel@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: FDA is amending the animal drug regulations 
in 21 CFR 558.485 to correct an inadvertent omission in the list of 
concentrations of pyrantel tartrate Type A medicated articles approved 
for use by Phibro Animal Health. This action is being taken to improve 
the accuracy of the animal drug regulations.
    This rule does not meet the definition of ``rule'' in 5 U.S.C. 
804(3)(A) because it is a rule of ``particular applicability.'' 
Therefore, it is not subject to the congressional review requirements 
in 5 U.S.C. 801-808.

List of Subjects in 21 CFR Part 558

    Animal drugs, Animal feeds.

0
Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
authority delegated to the Commissioner of Food and Drugs and 
redelegated to the Center for Veterinary Medicine, 21 CFR part 558 is 
amended as follows:

PART 558--NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS

0
1. The authority citation for 21 CFR part 558 continues to read as 
follows:

    Authority: 21 U.S.C. 360b, 371.


Sec.  558.485   [Amended]

0
2. In Sec.  558.485, in paragraph (b)(1), add ``48,'' in numerical 
sequence.

    Dated: March 12, 2008.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. E8-5928 Filed 3-24-08; 8:45 am]
BILLING CODE 4160-01-S