2010-27287. New Animal Drugs; Change of Sponsor; Monensin Blocks  

  • Start Preamble

    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Final rule.

    SUMMARY:

    The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect a change of sponsor from Farmland Industries, Inc., to Land O' Lakes Purina Feed LLC for a free-choice supplement block containing monensin for pasture cattle.

    DATES:

    This rule is effective October 28, 2010.

    Start Further Info

    FOR FURTHER INFORMATION CONTACT:

    Steven D. Vaughn, Center for Veterinary Medicine (HFV-100), Food and Drug Administration, 7520 Standish Pl., Rockville, MD 20855, 240-276-8300, e-mail: steven.vaughn@fda.hhs.gov.

    End Further Info End Preamble Start Supplemental Information

    SUPPLEMENTARY INFORMATION:

    Farmland Industries, Inc., Kansas City, MO 64116, has informed FDA that it has transferred ownership of, and all rights and interest in, NADA 118-509 for Pasture Gainer Block-37 R350 (monensin) to Land O' Lakes Purina Feed LLC, 100 Danforth Dr., Gray Summit, MO 63039. Accordingly, the regulations are amended in 21 CFR 520.1448a to reflect this change of sponsorship.

    Following this change of sponsorship, Farmland Industries, Inc., is no longer the sponsor of an approved application. Accordingly, § 510.600 (21 CFR 510.600) is being amended to remove the entries for this firm.

    In addition, Land O' Lakes Purina Feed LLC is not currently listed in the animal drug regulations as a sponsor of an approved application. Accordingly, § 510.600 is being amended to add entries for this sponsor.

    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.

    Start List of Subjects

    List of Subjects

    21 CFR Part 510

    • Administrative practice and procedure
    • Animal drugs
    • Labeling
    • Reporting and recordkeeping requirements

    21 CFR Part 520

    • Animal drugs
    End List of Subjects Start Amendment Part

    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 parts 510 and 520 are amended as follows:

    End Amendment Part Start Part

    PART 510—NEW ANIMAL DRUGS

    End Part Start Amendment Part

    1. The authority citation for 21 CFR part 510 continues to read as follows:

    End Amendment Part Start Authority

    Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e.

    End Authority Start Amendment Part

    2. In § 510.600, in the table in paragraph (c)(1), remove the entry for “Farmland Industries, Inc.”, and alphabetically add a new entry for “Land O' Lakes Purina Feed LLC”; and in the table in paragraph (c)(2), remove the entry for “021676” and numerically add an entry for “066071” to read as follows:

    End Amendment Part
    Start Printed Page 66305
    Names, addresses, and drug labeler codes of sponsors of approved applications.
    * * * * *

    (c) * * *

    (1) * * *

    Firm name and addressDrug labeler code
    *    *    *    *    *
    Land O' Lakes Purina Feed LLC, 100 Danforth Dr., Gray Summit, MO 63039066071
    *    *    *    *    *

    (2) * * *

    Drug labeler codeFirm name and address
    *    *    *    *    *
    066071Land O' Lakes Purina Feed LLC, 100 Danforth Dr., Gray Summit, MO 63039.
    *    *    *    *    *
    Start Part

    PART 520—ORAL DOSAGE FORM NEW ANIMAL DRUGS

    End Part Start Amendment Part

    3. The authority citation for 21 CFR part 520 continues to read as follows:

    End Amendment Part Start Authority

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

    End Authority
    [Amended]
    Start Amendment Part

    4. Section 520.1448a is amended in paragraph (c)(2) by removing “021676” and by adding in its place “No. 066071”.

    End Amendment Part Start Signature

    Dated: October 21, 2010.

    Elizabeth Rettie,

    Deputy Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.

    End Signature End Supplemental Information

    [FR Doc. 2010-27287 Filed 10-27-10; 8:45 am]

    BILLING CODE 4160-01-P

Document Information

Comments Received:
0 Comments
Effective Date:
10/28/2010
Published:
10/28/2010
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
2010-27287
Dates:
This rule is effective October 28, 2010.
Pages:
66304-66305 (2 pages)
Docket Numbers:
Docket No. FDA-2010-N-0002
Topics:
Administrative practice and procedure, Animal drugs, Labeling, Reporting and recordkeeping requirements
PDF File:
2010-27287.pdf
CFR: (2)
21 CFR 510.600
21 CFR 520.1448a