{"abstract":"The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect revised human food safety warnings on dosage form new animal drug product labeling that have not been codified. The regulations are also being amended to correct the wording of certain other conditions of use, to correct minor errors, and to revise some sections to reflect a current format. These actions are being taken to comply with the Federal Food, Drug, and Cosmetic Act (the FD&C Act) and to improve the accuracy and readability of the regulations.","action":"Final rule; correcting amendments.","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/2011/08/25/2011-21721.html","cfr_references":[{"chapter":null,"citation_url":null,"part":520,"title":21},{"chapter":null,"citation_url":null,"part":522,"title":21}],"citation":"76 FR 53050","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"This rule is effective August 25, 2011.","disposition_notes":null,"docket_ids":["Docket No. FDA-2011-N-0003"],"dockets":[],"document_number":"2011-21721","effective_on":"2011-08-25","end_page":53051,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2011/08/25/2011-21721.xml","html_url":"https://www.federalregister.gov/documents/2011/08/25/2011-21721/new-animal-drugs-ampicillin-trihydrate-bacitracin-methylene-disalicylate-flunixin-gonadotropin","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2011-21721?publication_date=2011-08-25","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2011-08-25/2011-21721/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":236,"last_updated":"2026-04-04 16:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2011-08-25/pdf/2011-21721.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2011-08-25","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2011/08/25/2011-21721.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[{"title":"Freedom of Information Summary NADA 141-324 Phenylpropanolamine","document_id":"FDA-2011-N-0003-0081"},{"title":"Freedom of Information Summary NADA 141-331 Pergolide","document_id":"FDA-2011-N-0003-0080"},{"title":"Freedom of Information Summary NADA 141-333 - Milbemycin Oxime, Lufenuron, and Praziquantel","document_id":"FDA-2011-N-0003-0072"},{"title":"Freedom of Information Summary NADA 095-735 - Monensin","document_id":"FDA-2011-N-0003-0069"},{"title":"Freedom of Information Summary NADA 141-207 - Danofloxacin","document_id":"FDA-2011-N-0003-0067"},{"title":"Freedom of Information Summary NADA 141-322 - Gonadotropin Releasing Factor Analog-Diphtheria Toxoid Conjugate","document_id":"FDA-2011-N-0003-0065"},{"title":"Freedom of Information Summary ANDA 200-494 - Gentamicin Sulfate","document_id":"FDA-2011-N-0003-0063"},{"title":"reedom of Information Summary NADA 141-203 Deracoxib","document_id":"FDA-2011-N-0003-0061"},{"title":"Gentamicin Topical Spray (gentamicin sulfate, betamethasone valerate- ANADA 200-416; Freedom of Information Summary","document_id":"FDA-2011-N-0003-0059"},{"title":"Freedom of Information Summary ANDA 200-318 Bimectin Pour-On (Ivermectin)","document_id":"FDA-2011-N-0003-0057"}],"comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2011-N-0003","supporting_documents_count":32,"docket_id":"FDA-2011-N-0003","regulation_id_number":null,"title":"NADA/ANADA Notices","checked_regulationsdotgov_at":"2011-09-14T08:09:41Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":53050,"subtype":null,"title":"New Animal Drugs; Ampicillin Trihydrate, Bacitracin Methylene Disalicylate, Flunixin, Gonadotropin Releasing Factor Analog-Diphtheria Toxoid Conjugate, Methylprednisolone, and Sulfamethazine","toc_doc":"Ampicillin Trihydrate, Bacitracin Methylene Disalicylate, Flunixin, etc.; Correcting Amendments","toc_subject":"New Animal Drugs:","topics":["Animal drugs"],"type":"Rule","volume":76}