{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\" and docket_id = \"FDA-2022-N-2390\" sorted by posted_date descending", "rows": [["FDA-2022-N-2390-0587", "FDA", "FDA-2022-N-2390", "Vanda Hearing Request for sNDA 205677-004 (tasimelteon)", "Other", "Request for Hearing", "2026-02-26T05:00:00Z", 2026, 2, "2026-02-26T05:00:00Z", null, "2026-02-27T00:15:15Z", null, 0, 0, "09000064b91df99f"], ["FDA-2022-N-2390-0586", "FDA", "FDA-2022-N-2390", "Vanda Hearing Request for sNDA 205677-004 (tasimelteon)", "Other", "Request for Hearing", "2026-02-09T05:00:00Z", 2026, 2, "2026-02-09T05:00:00Z", null, "2026-02-09T23:37:26Z", null, 0, 0, "09000064b919a1ca"], ["FDA-2022-N-2390-0585", "FDA", "FDA-2022-N-2390", "Revised Letter re: CDER and Vanda\u2019s Joint Request", "Other", "Letter(s)", "2025-10-21T04:00:00Z", 2025, 10, "2025-10-21T04:00:00Z", null, "2025-10-21T17:13:39Z", null, 0, 0, "09000064b903ed93"], ["FDA-2022-N-2390-0584", "FDA", "FDA-2022-N-2390", "Letter from FDA OC to Vanda Pharmaceuticals Inc. and FDA CDER", "Other", "Letter(s)", "2025-10-15T04:00:00Z", 2025, 10, "2025-10-15T04:00:00Z", null, "2025-10-15T15:52:08Z", null, 0, 0, "09000064b9015606"], ["FDA-2022-N-2390-0581", "FDA", "FDA-2022-N-2390", "Vanda Pharmaceuticals Inc.'s Submission in Support of Summary Judgment to the Applicant or a Hearing on Approvability", "Other", "Brief", "2025-03-07T05:00:00Z", 2025, 3, "2025-03-07T05:00:00Z", null, "2025-10-15T15:05:12Z", null, 0, 0, "09000064869b6834"], ["FDA-2022-N-2390-0161", "FDA", "FDA-2022-N-2390", "Notice of the Denial of a Hearing Request Regarding a Proposal To Refuse To Approve a Supplemental New Drug Application for HETLIOZ (Tasimelteon)", "Notice", "Notice of Denial", "2025-03-07T05:00:00Z", 2025, 3, "2025-03-07T05:00:00Z", null, "2025-03-07T14:52:35Z", "2025-03697", 0, 0, "09000064869b9231"], ["FDA-2022-N-2390-0580", "FDA", "FDA-2022-N-2390", "Cover Letter from Vanda Pharmaceuticals Inc.", "Other", "Letter(s)", "2025-03-07T05:00:00Z", 2025, 3, "2025-03-07T05:00:00Z", null, "2025-10-15T15:04:57Z", null, 0, 0, "09000064869b682f"], ["FDA-2022-N-2390-0582", "FDA", "FDA-2022-N-2390", "Declaration of Thomas Roth", "Other", "Declaration(s)", "2025-03-07T05:00:00Z", 2025, 3, "2025-03-07T05:00:00Z", null, "2025-10-15T15:05:31Z", null, 0, 0, "09000064869b6836"], ["FDA-2022-N-2390-0583", "FDA", "FDA-2022-N-2390", "Declaration of Daniel Combs", "Other", "Declaration(s)", "2025-03-07T05:00:00Z", 2025, 3, "2025-03-07T05:00:00Z", null, "2025-10-15T15:05:43Z", null, 0, 0, "09000064869b6838"], ["FDA-2022-N-2390-0132", "FDA", "FDA-2022-N-2390", "Vanda Pharmaceuticals Inc.\u2019s Submission in Support of Summary Judgment to the Applicant or a Hearing on Approvability of Tasimelteon to Treat Insomnia Associated with Difficulties with Sleep Initiation", "Other", "Brief", "2025-03-04T05:00:00Z", 2025, 3, "2025-03-04T05:00:00Z", null, "2025-03-04T14:31:50Z", null, 0, 0, "0900006486972393"], ["FDA-2022-N-2390-0133", "FDA", "FDA-2022-N-2390", "First Declaration of Thomas Roth", "Other", "Declaration(s)", "2025-03-04T05:00:00Z", 2025, 3, "2025-03-04T05:00:00Z", null, "2025-03-04T14:31:56Z", null, 0, 0, "09000064869723be"], ["FDA-2022-N-2390-0135", "FDA", "FDA-2022-N-2390", "Agency Decision Hetlioz for Insomnia", "Other", "Agency Response", "2025-03-04T05:00:00Z", 2025, 3, "2025-03-04T05:00:00Z", null, "2025-03-04T14:32:32Z", null, 0, 0, "0900006486995bdc"], ["FDA-2022-N-2390-0134", "FDA", "FDA-2022-N-2390", "Second Declaration of Thomas Roth", "Other", "Declaration(s)", "2025-03-04T05:00:00Z", 2025, 3, "2025-03-04T05:00:00Z", null, "2025-03-04T14:32:01Z", null, 0, 0, "09000064869723c0"], ["FDA-2022-N-2390-0131", "FDA", "FDA-2022-N-2390", "Cover Letter from Vanda Pharmaceuticals Inc.", "Other", "Letter(s)", "2025-03-04T05:00:00Z", 2025, 3, "2025-03-04T05:00:00Z", null, "2025-03-04T14:31:42Z", null, 0, 0, "090000648697238f"], ["FDA-2022-N-2390-0130", "FDA", "FDA-2022-N-2390", "CDER Proposed Order_ Docket No. FDA-2022-N-2390 (Vanda Pharmaceuticals Inc. 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