2013-20616. Withdrawal of Approval of New Animal Drug Applications; Quali-Tech Products, Inc.; Bambermycins; Pyrantel; Tylosin; Virginiamycin  

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    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Final rule.

    SUMMARY:

    The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect the withdrawal of approval of four new animal drug applications (NADAs), held by Quali-Tech Products, Inc., at the sponsor's request because the products are no longer manufactured or marketed.

    DATES:

    The rule is effective September 3, 2013.

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    FOR FURTHER INFORMATION CONTACT:

    David Alterman, Center for Veterinary Medicine (HFV-212), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-453-6843, david.alterman@fda.hhs.gov.

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    SUPPLEMENTARY INFORMATION:

    Quali-Tech Products, Inc., has requested that FDA withdraw approval of the following four NADAs because the products, used to manufacture Type C medicated feeds, are no longer manufactured or marketed: NADA 097-980 for Quali-Tech TYLAN-10 (tylosin phosphate) Premix, NADA 118-815 for Q.T. BAN-TECH (pyrantel tartrate), NADA 132-705 for FLAVOMYCIN (bambermycins), and NADA 133-335 for STAFAC (virginiamycin) Swine Pak 10.

    Elsewhere in this issue of the Federal Register, FDA gave notice that approval of NADAs 097-980, 118-815, 132-705, and 133-335, and all supplements and amendments thereto, is withdrawn. As provided in the regulatory text of this document, the animal drug regulations are amended to reflect these voluntary withdrawals of approval.

    Following these withdrawals of approval, Quali-Tech Products, Inc., will no longer be the sponsor of an approved application. Accordingly, 21 CFR 510.600(c) is being amended to remove the entries for this firm.

    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.

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    List of Subjects

    21 CFR Part 510

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

    21 CFR Parts 558

    • Animal drugs
    • Animal feeds
    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 parts 510 and 558 are amended as follows:

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    PART 510—NEW ANIMAL DRUGS

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

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

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    [Amended]
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    2. In § 510.600, in the table in paragraph (c)(1), remove the entry for “Quali-Tech Products, Inc.”; and in the table in paragraph (c)(2), remove the entry for “016968”.

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    PART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS

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

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

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    4. In § 558.95, revise paragraphs (a), (d)(1), (d)(2), (d)(3), (d)(4)(i), and (d)(4)(ii) to read as follows:

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    Bambermycins.

    (a) Approvals. See sponsors in § 510.600(c) of this chapter for use of Type A medicated articles as in paragraph (d) of this section:

    (1) No. 016592: 2, 4, and 10 grams per pound for use as in paragraphs (d)(1), (d)(2), (d)(3), and (d)(4) of this section.

    (2) Nos. 012286 and 017790: 2 grams for use as in paragraph (d)(2) of this section and 0.4 and 2 grams per pound for use as in paragraph (d)(3).

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    (d) * * *

    (1) Chickens. Use in medicated feed as follows:

    Bambermycins in grams/tonIndications for useLimitationsSponsor
    (i) 1 to 2Broiler chickens: For increased rate of weight gain and improved feed efficiencyFeed continuously as the sole ration016592.
    (ii) [Reserved]

    (2) Turkeys. Use in medicated feed as follows:

    Bambermycins in grams/tonIndications for useLimitationsSponsor
    (i) 1 to 2Growing turkeys: For improved feed efficiencyFeed continuously as the sole ration012286, 016592, 017790.
    (ii) 2Growing turkeys: For increased rate of weight gain and improved feed efficiencyFeed continuously as the sole ration012286, 016592, 017790.
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    (3) Swine. Use in medicated feed as follows:

    Bambermycins in grams/tonIndications for useLimitationsSponsor
    (i) 2Growing-finishing swine: For increased rate of weight gain and improved feed efficiencyFeed continuously as the sole ration012286, 016592, 017790.
    (ii) 2 to 4Growing-finishing swine: For increased rate of weightFeed continuously as the sole ration012286, 016592, 017790.

    (4) Cattle. Use in medicated feed as follows:

    Bambermycins in grams/tonIndications for useLimitationsSponsor
    (i) 1 to 4Cattle fed in confinement for slaughter: For increased rate of weight gain and improved feed efficiencyFeed continuously at a rate of 10 to 20 milligrams per head per day016592.
    (ii) 2 to 40Pasture cattle (slaughter, stocker, and feeder cattle, and dairy and beef replacement heifers): For increased rate of weight gainFeed continuously at a rate of 10 to 40 milligrams per head per day in at least 1 pound and not more than 10 pounds of feed. Daily bambermycins intakes in excess of 20 mg/head/day have not been shown to be more effective than 20 mg/head/day016592.
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    5. In paragraph (b)(3) of § 558.485, remove “Nos. 016968, and 017790” and in its place add “No. 017790”.

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    6. In § 558.625, remove and reserve paragraph (b)(14).

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    [Amended]
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    7. In paragraph (a)(2) of § 558.635, remove “046573, 016968, and 017790” and in its place add “046573 and 017790”.

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    Dated: August 20, 2013.

    Bernadette Dunham,

    Director, Center for Veterinary Medicine.

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    [FR Doc. 2013-20616 Filed 8-22-13; 8:45 am]

    BILLING CODE 4160-01-P

Document Information

Effective Date:
9/3/2013
Published:
08/23/2013
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
2013-20616
Dates:
The rule is effective September 3, 2013.
Pages:
52430-52431 (2 pages)
Docket Numbers:
Docket No. FDA-2013-N-0002
Topics:
Administrative practice and procedure, Animal drugs, Animal feeds, Labeling, Reporting and recordkeeping requirements
PDF File:
2013-20616.pdf
Supporting Documents:
» FREEDOM OF INFORMATION SUMMARY NADA 130-185 AMPROL 25% and FLAVOMYCIN Amprolium and Bambermycins
» FREEDOM OF INFORMATION SUMMARY Application Number 141-422 PACCAL VET-CA1 Paclitaxel for injection Powder for Injection Dog
» FREEDOM OF INFORMATION SUMMARY NADA141-420 TILDREN tiludronate disodium Powder for injection Horse
» FREEDOM OF INFORMATION SUMMARY NADA 141-361 PULMOTIL AC Tilmicosin Phosphate Aqueous Concentrate Swine
» FREEDOM OF INFORMATION SUMMARY NADA 141-246 AQUAFLOR Florfenicol
» Freedom of Information Summary NADA 141-288 EXCENEL RTU EZ Ceftiofur Hydrochloride
» Freedom of Information Summary NADA 095-735 RUMENSIN 90 Monensin
» Freedom of Information Summary NADA 141-406 NEXGARD Afoxolaner Chewable Tablet
» Freedom of Information Summary ANADA 200-548 ACTOGAIN 45 Ractopamine Hydrochloride Cattle fed in confinement for slaughter
» Freedom of Information Summary ANADA 200-542 ENGAIN 9 and ENGAIN 5 Ractopamine Hydrochloride Finishing Swine
CFR: (5)
21 CFR 510.600
21 CFR 558.95
21 CFR 558.485
21 CFR 558.625
21 CFR 558.635