{"database": "openregs", "table": "documents", "rows": [["FDA-2016-N-0735-0001", "FDA", "FDA-2016-N-0735", "Agency Information Collection Activities; Proposed Collection; Comment Request; Superimposed Text in Direct-to-Consumer Promotion of Prescription Drugs", "Notice", "60 Day Proposed Information Collection", "2016-03-09T05:00:00Z", 2016, 3, "2016-03-09T05:00:00Z", "2016-05-10T03:59:59Z", "2016-05-09T16:00:58Z", "2016-05233", 0, 0, "0900006481eb4f07"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2016-N-0735-0001"], "units": {}, "query_ms": 17.935351002961397, "source": "Federal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"}