2012-3747. Animal Drugs, Feeds, and Related Products; N-Methyl-2-Pyrrolidone; Correction  

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    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Final rule; correcting amendment.

    SUMMARY:

    The Food and Drug Administration (FDA) published a document in the Federal Register of November 25, 2011 (76 FR 72617), codifying a method of detection for residues of n-methyl-2-pyrrolidone in edible tissues of cattle. That document contained a universal resource locator (URL) linking to the Agency's Web site that did not reflect the most recent URL.

    DATES:

    This correction is effective February 17, 2012.

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    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, george.haibel@fda.hhs.gov.

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    SUPPLEMENTARY INFORMATION:

    In the Federal Register of November 25, 2011 (76 FR 72617), FDA issued a final rule codifying a method of detection for residues of n-methyl-2-pyrrolidone in edible tissues of cattle. That document contained a universal resource locator (URL) linking to the Agency's Web site that did not reflect the most recent URL. This document corrects the URL.

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    List of Subjects in 21 CFR Part 500

    • Animal drugs
    • Animal feeds
    • Cancer
    • Labeling
    • Packaging and containers
    • Polychlorinated biphenyls (PCBs)
    • Incorporation by reference
    End List of Subjects

    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 500 is amended as follows:

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    PART 500—GENERAL

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    1. The authority citation for 21 CFR part 500 continues to read as follows:

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    Authority: 21 U.S.C. 321, 331, 342, 343, 348, 351, 352, 353, 360b, 371.

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    2. Section 500.1410 is amended in paragraph (a) by revising the third sentence to read as follows:

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    N-methyl-2-pyrrolidone.

    (a) * * * You may obtain a copy of the method from the Communications Staff (HFV-12), Center for Veterinary Medicine, Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9120; or go to http://www.fda.gov/​AboutFDA/​CentersOffices/​OfficeofFoods/​CVM/​CVMFOIAElectronicReadingRoom/​default.htm. * * *

    * * * * *
    Start Signature

    Dated: February 13, 2012.

    William T. Flynn,

    Acting Director, Center for Veterinary Medicine.

    End Signature End Supplemental Information

    [FR Doc. 2012-3747 Filed 2-16-12; 8:45 am]

    BILLING CODE 4160-01-P

Document Information

Effective Date:
2/17/2012
Published:
02/17/2012
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule; correcting amendment.
Document Number:
2012-3747
Dates:
This correction is effective February 17, 2012.
Pages:
9528-9528 (1 pages)
Docket Numbers:
Docket No. FDA-2011-N-0003
Topics:
Animal drugs, Animal feeds, Cancer, Incorporation by reference, Labeling, Packaging and containers, Polychlorinated biphenyls (PCB's)
PDF File:
2012-3747.pdf
Supporting Documents:
» Freedom of Information Summary NADA 141-324 Phenylpropanolamine
» Freedom of Information Summary NADA 141-331 Pergolide
» Freedom of Information Summary NADA 141-333 - Milbemycin Oxime, Lufenuron, and Praziquantel
» Freedom of Information Summary NADA 095-735 - Monensin
» Freedom of Information Summary NADA 141-207 - Danofloxacin
» Freedom of Information Summary NADA 141-322 - Gonadotropin Releasing Factor Analog-Diphtheria Toxoid Conjugate
» Freedom of Information Summary ANDA 200-494 - Gentamicin Sulfate
» reedom of Information Summary NADA 141-203 Deracoxib
» Gentamicin Topical Spray (gentamicin sulfate, betamethasone valerate- ANADA 200-416; Freedom of Information Summary
» Freedom of Information Summary ANDA 200-318 Bimectin Pour-On (Ivermectin)
CFR: (1)
21 CFR 500.1410