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withdrawn,object_id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-2008-N-0500-0010,FDA,FDA-2008-N-0500,"Agency Information Collection Activities; Announcement of Office of
Management and Budget Approvals",Notice,Notice of Approval,2019-11-22T05:00:00Z,2019,11,2019-11-22T05:00:00Z,,2019-11-22T16:44:23Z,2019-07467,0,0,0900006483bad4cf
FDA-2008-N-0500-0009,FDA,FDA-2008-N-0500,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; General Licensing
Provisions; Requirements on Content and Format of Labeling for Human
Prescription Drug and Biological Products",Notice,30 Day Proposed Information Collection,2018-11-21T05:00:00Z,2018,11,2018-11-21T05:00:00Z,2018-12-22T04:59:59Z,2018-11-21T13:19:42Z,2018-25352,0,0,09000064838f1a72
FDA-2008-N-0500-0006,FDA,FDA-2008-N-0500,Agency Information Collection Activities; Proposed Collection; Comment Request; Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products,Notice,60 Day Proposed Information Collection,2018-07-20T04:00:00Z,2018,7,2018-07-20T04:00:00Z,2018-09-19T03:59:59Z,2018-09-19T01:06:35Z,2018-15512,0,0,09000064835263c7
FDA-2008-N-0500-0004,FDA,FDA-2008-N-0500,"Agency Information Collection Activities; Submission for Office 
of Management and Budget Review; Comment Request; Requirements on Content and Format of Labeling for Human Prescription Drug and 
Biological Products",Notice,30 Day Proposed Information Collection,2015-05-29T04:00:00Z,2015,5,2015-05-29T04:00:00Z,2015-06-30T03:59:59Z,2015-05-29T13:09:10Z,2015-12957,0,0,0900006481b0d10f
FDA-2008-N-0500-0003,FDA,FDA-2008-N-0500,"Agency Information Collection Activities; Proposed Collection;
Comment Request; Requirements on Content and Format of Labeling for
Human Prescription Drug and Biological Products",Notice,60 Day Proposed Information Collection,2015-01-21T05:00:00Z,2015,1,2015-01-21T05:00:00Z,2015-03-24T03:59:59Z,2015-03-24T02:08:51Z,2015-00761,0,0,09000064819d54c5
FDA-2008-N-0500-0002,FDA,FDA-2008-N-0500,Agency Information Collection Activities; Proposed Collection; Comment Request; Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products,Notice,30 Day Proposed Information Collection,2009-01-09T05:00:00Z,2009,1,2009-01-09T05:00:00Z,2009-02-10T04:59:59Z,2015-01-09T17:16:17Z,E9-00175,0,0,090000648081956b
FDA-2008-N-0500-0001,FDA,FDA-2008-N-0500,Agency Information Collection Activities; Proposed Collection; Comment Request; Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products,Notice,N-Notice,2008-09-29T04:00:00Z,2008,9,2008-09-29T04:00:00Z,2008-11-29T04:59:59Z,2015-01-09T17:05:22Z,E8-22731,0,0,090000648072c52b