{"database": "openregs", "table": "documents", "rows": [["FDA-1978-N-0021-0014", "FDA", "FDA-1978-N-0021", "Notice of Proposed Rulemaking re Laxative Drug Products for Over-the-Counter Human Use; Reopening of the Administrative Record", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2003-10-23T04:00:00Z", 2003, 10, "2003-10-22T04:00:00Z", "2004-01-21T04:59:59Z", "2016-08-09T20:43:30Z", null, 0, 0, "090000648055d669"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-1978-N-0021-0014"], "units": {}, "query_ms": 0.5696290172636509, "source": "Federal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"}