{"database": "openregs", "table": "documents", "rows": [["FDA-2013-P-1609-0004", "FDA", "FDA-2013-P-1609", "Determination That LUPRON DEPOT (Leuprolide Acetate for Depot\nSuspension), Injectable 3.75 Milligrams/Vial Was Not Withdrawn\nFrom Sale for Reasons of Safety or Effectiveness", "Notice", "Determinations", "2014-10-08T04:00:00Z", 2014, 10, "2014-10-08T04:00:00Z", null, "2015-03-24T20:25:17Z", "2014-23961", 0, 0, "09000064818b1b12"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2013-P-1609-0004"], "units": {}, "query_ms": 0.36652316339313984, "source": "Federal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"}