98-15554. Ophthalmic and Topical Dosage Form New Animal Drugs; Gentamicin Sulfate, Betamethasone Valerate, and Clotrimazole Ointment  

  • [Federal Register Volume 63, Number 112 (Thursday, June 11, 1998)]
    [Rules and Regulations]
    [Pages 31931-31932]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-15554]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Parts 510 and 524
    
    
    Ophthalmic and Topical Dosage Form New Animal Drugs; Gentamicin 
    Sulfate, Betamethasone Valerate, and Clotrimazole Ointment
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule.
    
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    SUMMARY: The Food and Drug Administration (FDA) is amending the animal 
    drug regulations to reflect approval of an abbreviated new animal drug 
    application (ANADA) filed by Med-Pharmex, Inc. The ANADA provides for 
    the use of gentamicin sulfate, betamethasone valerate, and clotrimazole 
    (Tri-Otic ointment) for the treatment of canine acute and chronic 
    otitis externa associated with yeast and/or bacteria susceptible to 
    gentamicin.
    
    EFFECTIVE DATE: June 11, 1998.
    FOR FURTHER INFORMATION CONTACT: Dianne T. McRae, Center for Veterinary 
    Medicine (HFV-102), Food and Drug Administration, 7500 Standish Pl., 
    Rockville, MD 20855, 301-594-1623.
    
    SUPPLEMENTARY INFORMATION: Med-Pharmex, Inc., 2727 Thompson Creek Rd., 
    Pomona, CA 91767, filed ANADA 200-229 that provides for the use of 
    gentamicin sulfate, betamethasone valerate, and clotrimazole (Tri-Otic 
    ointment) for the treatment of canine acute and chronic otitis externa 
    associated with yeast and/or bacteria susceptible to gentamicin.
        The ANADA is approved as a generic copy of Schering Plough Animal 
    Health Corp.'s NADA 140-896 for OTOMAX (gentamicin sulfate, 
    betamethasone valerate, and clotrimazole). ANADA 200-229 is approved as 
    of April 8, 1998, and the regulations are amended in 21 CFR 524.1044g 
    to reflect the approval. The basis for approval is discussed in the 
    freedom of information summary. In addition, the agency is amending 21 
    CFR 510.600(c)( 1) and (c)(2) to reflect a change of sponsor's name and 
    address.
        In accordance with the freedom of information provisions of 21 CFR 
    part 20 and 514.11(e)(2)(ii), a summary of safety and effectiveness 
    data and information submitted to support approval of this application 
    may be seen in the Dockets Management Branch (HFA-305), Food and Drug 
    Administration, 12420 Parklawn Dr., rm. 1-23, Rockville, MD 20857, 
    between 9 a.m. and 4 p.m., Monday through Friday.
        The agency has determined under 21 CFR 25.33(d)(1) that this action 
    is of a type that does not individually or cumulatively have a 
    significant effect on the human environment. Therefore, neither an 
    environmental assessment nor an environmental impact statement is 
    required.
    
    List of Subjects
    
    21 CFR Part 510
    
        Administrative practice and procedure, Animal drugs, Labeling, 
    Reporting and recordkeeping requirements.
    
    21 CFR Part 524
    
        Animal drugs.
        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 
    524 are amended as follows:
    
    PART 510--NEW ANIMAL DRUGS
    
        1. The authority citation for 21 CFR part 510 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e.
    
        2. Section 510.600  Names, addresses, and drug labeler codes of 
    sponsors of approved applications is amended in the table in paragraph 
    (c)(1) in the entry for ``Med-Pharmex, Inc., Biomed Laboratories'' and 
    in the table in paragraph (c)(2) in the entry for ``051259'' by 
    revising the sponsor name and address to read as follows:
    
    
    Sec. 510.600   Names, addresses, and drug labeler codes of sponsors of 
    approved applications.
    
    * * * * *
        (c) * * *
        (1) * * *
    
                                                                                                                    
    ----------------------------------------------------------------------------------------------------------------
                     Firm name and address                                      Drug labeler code                   
    ----------------------------------------------------------------------------------------------------------------
      *                    *                    *                    *                    *                    *    
                                                                 *                                                  
    Med-Pharmex, Inc., 2727 Thompson Creek Rd., Pomona, CA   051259                                                 
     91767-1861                                                                                                     
      *                    *                    *                    *                    *                    *    
                                                                 *                                                  
    ----------------------------------------------------------------------------------------------------------------
    
        (2) * * *
    
                                                                                                                    
    ----------------------------------------------------------------------------------------------------------------
                       Drug labeler code                                      Firm name and address                 
    ----------------------------------------------------------------------------------------------------------------
      *                    *                    *                    *                    *                    *    
                                                                 *                                                  
    051259                                                   Med-Pharmex, Inc., 2727 Thompson Creek Rd., Pomona, CA 
                                                              91767-1861                                            
      *                    *                    *                    *                    *                    *    
                                                                 *                                                  
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    [[Page 31932]]
    
    PART 524--OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS
    
        3. The authority citation for 21 CFR part 524 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 360b.
    
    Sec. 524.1044g   [Amended]
    
        4. Section 524.1044g Gentamicin sulfate, betamethasone valerate, 
    clotrimazole ointment is amended in paragraph (b) by removing 
    ``000061'' and adding in its place ``000061 and 051259''.
    
        Dated: May 27, 1998.
    Stephen F. Sundlof,
    Director, Center for Veterinary Medicine.
    [FR Doc. 98-15554 Filed 6-10-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
06/11/1998
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
98-15554
Dates:
June 11, 1998.
Pages:
31931-31932 (2 pages)
PDF File:
98-15554.pdf
CFR: (2)
21 CFR 510.600
21 CFR 524.1044g