documents: FDA-2022-N-2390-0042

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2022-N-2390-0042 FDA FDA-2022-N-2390 Scheduling for Vanda’s Hearing on Proposal to Refuse to Approve a New Drug Application Supplement for HETLIOZ (tasimelteon) Other Letter(s) 2024-09-10T04:00:00Z 2024 9 2024-09-10T04:00:00Z   2024-09-10T20:40:25Z   0 0 09000064866e4df2

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