{"abstract":"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 Cross Vetpharm Group Ltd. The ANADA provides for use of sulfamethazine soluble powder to create a solution administered as a drench to swine or cattle, or in the drinking water of chickens, turkeys, swine, or cattle for the treatment of coccidiosis or various bacterial diseases.","action":"Final rule.","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2006/12/04/E6-20404.html","cfr_references":[{"chapter":null,"citation_url":null,"part":520,"title":21}],"citation":"71 FR 70302","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"This rule is effective December 4, 2006.","disposition_notes":null,"docket_ids":[],"dockets":[],"document_number":"E6-20404","effective_on":"2006-12-04","end_page":70304,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2006/12/04/E6-20404.xml","html_url":"https://www.federalregister.gov/documents/2006/12/04/E6-20404/oral-dosage-form-new-animal-drugs-sulfamethazine-soluble-powder","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/E6-20404?publication_date=2006-12-04","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2006-12-04/E6-20404/mods.xml","not_received_for_publication":null,"page_length":3,"page_views":{"count":341,"last_updated":"2026-04-03 18:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2006-12-04/pdf/E6-20404.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2006-12-04","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2006/12/04/E6-20404.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"checked_regulationsdotgov_at":"2011-11-12T20:21:09Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":70302,"subtype":null,"title":"Oral Dosage Form New Animal Drugs; Sulfamethazine Soluble Powder","toc_doc":"Sulfamethazine soluble powder","toc_subject":"Animal drugs, feeds, and related products:","topics":["Animal drugs"],"type":"Rule","volume":71}