{"database": "openregs", "table": "documents", "rows": [["FDA-2014-N-0998-0008", "FDA", "FDA-2014-N-0998", "Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Regulations for In Vivo Radiopharmaceuticals Used for Diagnosis and Monitoring", "Notice", "30 Day Proposed Information Collection", "2021-04-14T04:00:00Z", 2021, 4, "2021-04-14T04:00:00Z", "2021-05-15T03:59:59Z", "2021-04-14T12:54:12Z", "2021-07639", 0, 0, "0900006484aa6edd"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2014-N-0998-0008"], "units": {}, "query_ms": 83.17629899829626, "source": "Federal Register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"}