01-22470. New Animal Drugs; Change of Sponsor  

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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 a change of sponsor for 56 approved new animal drug applications (NADAs) and 3 approved abbreviated new animal drug applications (ANADAs) from Roche Vitamins, Inc., to Alpharma, Inc.

    DATES:

    This rule is effective September 7, 2001.

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    FOR FURTHER INFORMATION CONTACT:

    Lonnie W. Luther, Center for Veterinary Medicine (HFV-102), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 301-827-0209.

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    SUPPLEMENTARY INFORMATION:

    Roche Vitamins, Inc., 45 Waterview Blvd., Parsippany, NJ 07054-1298, has informed FDA that it has transferred ownership of, and all rights and interest in, the following approved NADAs and ANADAs to Alpharma, Inc., One Executive Dr., P.O. Box 1399, Fort Lee, NJ 07024:

    NADA No.Product Name
    33-950Sulfamerazine in Fish Grade
    35-688Aureo SP-250; Aureomix 500
    35-805Aureomix-S 700 Crumbles; Aureomix-S 700
    36-361Amprolium Plus Ethopabate/CTC® Sodium Sulfate
    40-209Rofenaid® 40
    41-647Aureomix-S 700-A
    41-648Aureomix-S 700-D
    41-649Aureomix-S 700-G
    41-650Aureomix-S 700-E
    41-651Aureomix-S 700-F
    41-652Aureomix-S 700-C-2
    41-653Aureomix-S 700-B
    41-654Aureomix-S 700-H
    41-984Rofenaid® Plus Roxarsone
    46-920Baciferm® 10, 25, 40, and 50 Type A Medicated Articles
    48-486Robenz® Type A Medicated Article
    48-761Aureomycin® Type A Medicated Article
    49-287Chlorachel-50
    55-040SF Mix 66
    92-507Robenz® With Aureomycin® 500
    95-546Robenz® Plus Roxarsone
    96-298Avatec® and Bovatec® Premixes
    96-933Robenz® Plus Zn Bacitracin
    97-085Robenz® Plus Bac MD
    100-901Pfichlor 100S Milk Replacer Type A Medicated Article
    102-485Avatec®/3-Nitro®
    105-758Zinc Bacitracin and Amprol HI-E®
    107-996Avatec®/Fortracin® Premix
    112-661Avatec®/Lincomix®/3-Nitro®
    112-687Avatec®/Flavomycin®/3-Nitro®
    114-794Baciferm®/Amprol HI-E® Premix
    121-553Coban®/Aureomycin®
    123-154Coban®/3-Nitro®-10/Baciferm® Premix
    125-933Romet®-30 (Sulfamerazine)
    126-052Avatec®/Baciferm®/3-Nitro®
    128-686Bio-Cox® Type A Medicated Article
    131-894Avatec®/Fortracin®/3-Nitro® Broiler Premix
    132-447Bio-Cox® Plus Roxarsone
    134-185Bio-Cox®/3-Nitro®/Flavomycin®
    134-284Bio-Cox®/Flavomycin®
    135-321Bio-Cox®/3-Nitro®/BMD®
    135-746Bio-Cox®/BMD®
    136-484Carb-O-Sep®/Baciferm®
    137-536Bio-Cox®/3-Nitro® plus Albac®
    137-537Bio-Cox®/Lincomix®
    139-075Cygro® Type A Medicated Article
    139-190Bio-Cox®/3-Nitro®/Baciferm®
    139-235Bio-Cox®/Baciferm®
    140-579Bovatec®/Terramycin®
    140-581Bio-Cox®/3-Nitro®/Lincomix®
    140-859Aureomycin®/Bio-Cox®
    140-865Monteban®/Baciferm®
    140-867Aureomycin®/Bio-Cox®/3-Nitro®
    141-025Cattlyst® Type A Medicated Article
    141-109Avatec®/Baciferm®
    141-150Avatec®/Stafac®
    200-140Aureozol® Type A Medicated Article
    200-167Aureozol® 500 Granular
    200-242Aureomycin®-50, 70, 80, 90, 100/BMD® 25, 30, 40, 50, 60, 75

    Accordingly, the agency is amending the regulations in 21 CFR 558.58, 558.76, 558.78, 558.95, 558.120, 558.128, 558.140, 558.145, 558.155, 558.195, 558.305, 558.311, 558.340, 558.355, 558.363, 558.366, 558.515, 558.550, 558.575, 558.582, and 558.600 to reflect the transfer of ownership. Section 558.95 is also being amended to remove paragraph (d)(1)(x), an entry pertaining to NADA 112-687, which is redundant with § 558.311(e)(1)(ii). Other nonsubstantive changes are being made to remove incorrect drug labeler codes.

    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 Parts 522 and 524

    • Animal drugs

    21 CFR Part 558

    • Animal drugs
    • Animal feeds
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    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 522, 524, and 558 are amended as follows:

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    PART 522—IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS

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    1. The authority citation for 21 CFR part 522 continues to read as follows:

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

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    [Amended]
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    2. Section 522.575 Diazepam injection is amended in paragraph (b) by removing “000004” and by adding in its place “063238”.

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    PART 524—OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS

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    3. The authority citation for 21 CFR part 524 continues to read as follows:

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    Start Printed Page 46706 Authority: 21 U.S.C. 360b.

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    [Amended]
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    4. Section 524.520 Cuprimyxin cream is amended in paragraph (b) by removing “000004” and by adding in its place “063238”.

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    PART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS

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    5. 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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    [Amended]
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    6. Section 558.58 Amprolium and ethopabate is amended in the table in paragraph (d)(1)(iii), under the “Limitations” column in the entries for “Bacitracin 4 to 50”, “Bacitracin 5 to 35 plus roxarsone 34 (0.00375%)”, and “Bacitracin 10 to 50 plus roxarsone 15.4 to 45.4 (0.0017% to 0.005%)” by removing “Nos. 046573 and 063238” and by adding in its place “No. 046573”; and under the “Sponsor” column by removing “063238” and “and 063238” wherever they appear.

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    [Amended]
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    7. Section 558.76 Bacitracin methylene disalicylate is amended in the table in paragraph (d)(1)(iv), under the “Limitations” column by removing “Nos. 000004 and 046573” and by adding in its place “No. 046573”; and under the “Sponsor” column by removing “000004 and 046573” both times it appears and adding in its place “046573”.

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    8. Section 558.78 is amended by revising paragraph (a)(1), by removing paragraph (a)(2), and by redesignating paragraph (a)(3) as paragraph (a)(2); in the table in paragraphs (d)(1)(i) and (d)(1)(ii) under the “Sponsor” column by removing “063238”; and in paragraphs (d)(1)(v) and (d)(1)(vi) under the “Sponsor” column, and in paragraph (d)(2)(ii) by removing “063238” and by adding in its place “046573” to read as follows:

    Bacitracin zinc.

    (a) * * *

    (1) No. 046573: 10, 25, 40, and 50 grams per pound as in paragraph (d) of this section.

    * * * * *
    [Amended]

    9. Section 558.95 Bambermycins is amended by removing and reserving paragraph (d)(1)(x); and in paragraphs (d)(1)(xi) (b), (d)(1)(xii) (b), and (d)(1)(xiv) (b) by removing “063238” and by adding in its place “046573”.

    [Amended]

    10. Section 558.120 Carbarsone (not U.S.P.) is amended in paragraph (d)(1)(iii) (b) by removing “Nos. 046573 and 063238” and by adding in its place “No. 046573”.

    11. Section 558.128 is amended by revising paragraph (a); in the table in paragraph (d)(1) and in paragraph (d)(2) by removing “00004” or “000004” wherever they occur and by adding in their place “046573”; in paragraph (d)(1)(i) in entry 1, and in paragraphs (d)(1)(iv), (d)(1)(vi), and (d)(1)(viii) under the “Sponsor” column by removing “063238” and by adding in its place “046573”; in paragraph (d)(1)(i) in entry 2, and in paragraphs (d)(1)(ii), (d)(1)(iii), (d)(1)(v), (d)(1)(vii), (d)(1)(x), and (d)(1)(xii) in entry 3, and in paragraphs (d)(1)(xiv), (d)(1)(xvi), and (d)(1)(xvii) under the “Sponsor” column by removing “063238” to read as follows:

    Chlortetracycline.

    (a) Approvals. See sponsors in § 510.600(c) of this chapter for Type A medicated articles containing the following concentrations of either chlortetracycline calcium complex equivalent to chlortetracycline hydrochloride or, for products intended for use in milk replacer, chlortetracycline hydrochloride:

    (1) Nos. 000069, 046573, and 053389: 50 to 100 grams per pound.

    (2) No. 017519: 50 grams per pound.

    * * * * *
    [Amended]

    12. Section 558.140 Chlortetracycline and sulfamethazine is amended in paragraph (a) by removing “063238” and by adding in its place “046573”.

    [Amended]

    13. Section 558.145 Chlortetracycline, procaine penicillin, and sulfamethazine is amended in paragraph (a)(1) by removing “and 063238”, and in paragraph (a)(2) by removing “063238” and by adding in its place “046573”.

    [Amended]

    14. Section 558.155 Chlortetracycline, sulfathiazole, penicillin is amended in paragraph (a)(1) by removing “000004 and 000010” and adding in its place “Nos. 000010 and 046573”, and in paragraph (a)(2) by removing “000004 and 000010” and by adding in its place “000010 and 046573”.

    [Amended]

    15. Section 558.195 Decoquinate is amended in the table in paragraph (d) in the entry for “Roxarsone 11 to 45 (0.0012-0.005 pct.) plus Bacitracin 12 to 50” under the “Limitations” column by removing “Nos. 011716, 046573, and 063238” and by adding in its place “No. 046573”.

    [Amended]

    16. Section 558.305 Laidlomycin propionate potassium is amended in paragraph (a) by removing “063238” and by adding in its place “046573”.

    [Amended]

    17. Section 558.311 Lasalocid is amended in paragraphs (b) and (e) by removing “000004” or “063238” wherever they occur and by adding in their place “046573”.

    [Amended]

    18. Section 558.340 Maduramicin ammonium is amended in paragraph (a) by removing “063238” and by adding in its place “046573”.

    [Amended]

    19. Section 558.355 Monensin is amended in paragraphs (b)(8), (b)(9), (f)(1)(iv) (b), and (f)(1)(v) (b) by removing “063238” and by adding in its place “046573”; in paragraphs (f)(1)(xiv) (b) and (f)(1)(xvi) (b) by removing “Nos. 046573 and 063238” and by adding in its place “No. 046573”; and in paragraph (f)(1)(xv) (b) by removing “Nos. 063238 and 046573” and by adding in its place “No. 046573”.

    [Amended]

    20. Section 558.363 Narasin is amended in paragraphs (a)(7) and (d)(1)(x)(B) by removing “063238” and by adding in its place “046573”.

    [Amended]

    21. Section 558.366 Nicarbazin is amended in the table in paragraph (c) in the entry for the combination of nicarbazin at 113.5 grams per ton and bacitracin zinc at 4 to 50 grams per ton by removing “063238” in the “Limitations” column and by adding in its place “046573”.

    [Amended]

    22. Section 558.515 Robenidine hydrochloride is amended in paragraph (a) by removing “063238” and by adding in its place “046573”; in the table in paragraph (d) in the entry for robenidine hydrochloride at 30 grams per ton as a single ingredient by removing “063238” in the “Sponsor” column and by adding in its place “046573”; in the two entries for “Bacitracin (as bacitracin zinc)” by removing “063238” in the “Sponsor” column; and in the entry for “Chlortetracycline 500” by removing “063238” from the “Sponsor” column and by adding in its place “046573”.

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    [Amended]

    23. Section 558.550 Salinomycin is amended in paragraph (a)(1) by removing “063238” and by adding in its place “046573”; by removing paragraph (a)(3); in paragraph (d)(1)(xvii)(C) by removing “000004” and by adding in its place “046573”; in paragraphs (d)(1) and (d)(3) by removing “063238” wherever it occurs and by adding in its place “046573”; in paragraph (d)(1)(viii) (c) by removing “(b)(1)(iv) (c)” and by adding in its place “(d)(1)(iv) (c)”; and in paragraph (d)(1)(xi) (c) by removing “(b)(1)(x) (c)” and by adding in its place “(d)(1)(x) (c)”.

    [Amended]

    24. Section 558.575 Sulfadimethoxine, ormetoprim is amended in paragraphs (a)(1) and (a)(2) by removing “000004” and by adding in its place “046573”.

    [Amended]

    25. Section 558.582 Sulfamerazine is amended in paragraph (a) by removing “063238” and by adding in its place “046573”.

    [Amended]

    26. Section 558.600 Tiamulin is amended in paragraph (c)(4)(ii) by removing “046573, 053389, and 063238” and by adding in its place “046573 and 053389”.

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    Dated: August 24, 2001.

    Claire M. Lathers,

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

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    [FR Doc. 01-22470 Filed 9-6-01; 8:45 am]

    BILLING CODE 4160-01-S

Document Information

Effective Date:
9/7/2001
Published:
09/07/2001
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
01-22470
Dates:
This rule is effective September 7, 2001.
Pages:
46705-46707 (3 pages)
PDF File:
01-22470.pdf
CFR: (23)
21 CFR 522.575
21 CFR 524.520
21 CFR 558.58
21 CFR 558.76
21 CFR 558.78
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