{"database": "openregs", "table": "documents", "rows": [["FDA-2013-N-1558-0001", "FDA", "FDA-2013-N-1558", "Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry and Food and Drug Administration Staff; Section 905(j) Reports: Demonstrating Substantial Equivalence for Tobacco Products", "Notice", "60 Day Proposed Information Collection", "2013-12-27T05:00:00Z", 2013, 12, "2013-12-27T05:00:00Z", "2014-02-26T04:59:59Z", "2015-02-14T00:29:34Z", "2013-30880", 0, 0, "09000064814debdd"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2013-N-1558-0001"], "units": {}, "query_ms": 143.8604269642383, "source": "Federal Register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"}