{"database": "openregs", "table": "federal_register", "rows": [["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...", null]], "columns": ["document_number", "title", "type", "abstract", "publication_date", "pub_year", "pub_month", "html_url", "pdf_url", "agency_names", "agency_ids", "excerpts", "regulation_id_numbers"], "primary_keys": ["document_number"], "primary_key_values": ["E9-2941"], "units": {}, "query_ms": 137.75458093732595, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}