{"database": "openregs", "table": "documents", "rows": [["FDA-2006-P-0069-0003", "FDA", "FDA-2006-P-0069", "Letter from FDA CDER to Frommer, Lawrence & Haug LLP", "Other", "Letter(s)", "2007-02-08T05:00:00Z", 2007, 2, null, null, "2024-11-13T14:48:28Z", null, 0, 0, "0900006480444463"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2006-P-0069-0003"], "units": {}, "query_ms": 11.949609033763409, "source": "Federal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"}