federal_register: E9-2941

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts regulation_id_numbers
E9-2941 Implantation or Injectable Dosage Form New Animal Drugs; Flunixin Rule The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental abbreviated new animal drug application (ANADA) filed by Cross Vetpharm Group Ltd. The supplemental ANADA provides for the veterinary prescription use of flunixin meglumine solution by intravenous injection in dairy cattle for control of pyrexia associated with acute bovine mastitis. 2009-02-12 2009 2 https://www.federalregister.gov/documents/2009/02/12/E9-2941/implantation-or-injectable-dosage-form-new-animal-drugs-flunixin https://www.govinfo.gov/content/pkg/FR-2009-02-12/pdf/E9-2941.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental abbreviated new animal drug application (ANADA) filed by Cross Vetpharm Group Ltd. The supplemental ANADA provides for the veterinary...  

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