{"database": "lobbying", "table": "lobbying_activities", "rows": [[2866925, "68e1ec83-88d0-47f0-be87-365d3d88f791", "Q3", "AMERICAN VETERINARY MEDICAL ASSOCIATION", 3630, "AMERICAN VETERINARY MEDICAL ASSOCIATION", 2022, "third_quarter", "PHA", "Review of Food and Drug Administrations Final Guidance for industry #256: Compounding Animal Drugs from Bulk Drug Substances Review of Food and Drug Administrations Animal Generic Drug User Fee Act Reports Compounding Guidance (GFI 256) Animal Drug Fee Act/Animal Generic Drug User Fee Act reauthorization", "HOUSE OF REPRESENTATIVES,SENATE", 300000, null, 0, 0, "2022-10-17T08:28:12-04:00"]], "columns": ["id", "filing_uuid", "filing_type", "registrant_name", "registrant_id", "client_name", "filing_year", "filing_period", "issue_code", "specific_issues", "government_entities", "income_amount", "expense_amount", "is_no_activity", "is_termination", "received_date"], "primary_keys": ["id"], "primary_key_values": ["2866925"], "units": {}, "query_ms": 0.3929219674319029, "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"}