{"database": "openregs", "table": "documents", "rows": [["FDA-1978-N-0018-0755", "FDA", "FDA-1978-N-0018", "Supplement from Merck KGaA Attachment 1 Eusolex\u00ae 6300 Literature Review on Adverse Effects", "Supporting & Related Material", "Supplement", "2014-12-18T05:00:00Z", 2014, 12, null, null, "2014-12-18T19:43:26Z", null, 0, 0, "0900006481983e86"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-1978-N-0018-0755"], "units": {}, "query_ms": 0.5322719807736576, "source": "Federal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"}