{"database": "openregs", "table": "documents", "rows": [["FDA-2011-D-0074-0002", "FDA", "FDA-2011-D-0074", "Draft Guidance for Industry - Medication Guides; Distribution Requirements and Inclusion of Medication Guides in Risk Evaluation and Mitigation Strategies (REMS)", "Other", "GDL-Guidance", "2011-02-28T05:00:00Z", 2011, 2, "2011-02-28T05:00:00Z", null, "2019-10-21T13:22:59Z", null, 0, 0, "0900006480bfa33c"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2011-D-0074-0002"], "units": {}, "query_ms": 0.7055039750412107, "source": "Federal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"}