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documents: FDA-2013-N-1618-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2013-N-1618-0001 FDA FDA-2013-N-1618 Draft Prescription Drug User Fee Act V Information Technology Plan; Availability for Comment Notice General Notice 2013-12-26T05:00:00Z 2013 12 2013-12-26T05:00:00Z 2014-02-25T04:59:59Z 2024-11-07T23:00:00Z 2013-30818 1 0 09000064814dc9f4

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