{"database": "openregs", "table": "federal_register", "rows": [["2011-24461", "Oral Dosage Form New Animal Drugs; Tylosin", "Rule", "The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an original abbreviated new animal drug application (ANADA) filed by Cross Vetpharm Group, Ltd. The ANADA provides for use of tylosin tartrate soluble powder in chickens, turkeys, swine, and honey bees.", "2011-09-23", 2011, 9, "https://www.federalregister.gov/documents/2011/09/23/2011-24461/oral-dosage-form-new-animal-drugs-tylosin", "https://www.govinfo.gov/content/pkg/FR-2011-09-23/pdf/2011-24461.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 an original abbreviated new animal drug application (ANADA) filed by Cross Vetpharm Group, Ltd. The ANADA provides for use of tylosin tartrate soluble...", 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": ["2011-24461"], "units": {}, "query_ms": 0.29921112582087517, "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"}