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withdrawn,object_id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-2017-E-6002-0006,FDA,FDA-2017-E-6002,"Determination of Regulatory Review Period for Purposes of Patent
Extension; RUBRACA",Notice,Determinations,2018-12-28T05:00:00Z,2018,12,2018-12-28T05:00:00Z,2019-02-27T04:59:59Z,2018-12-31T21:05:16Z,2018-28217,0,0,09000064839cbe97
FDA-2017-E-6002-0005,FDA,FDA-2017-E-6002,Letter from FDA CDER to U.S. Patent and Trademark Office,Other,Letter(s),2018-12-21T05:00:00Z,2018,12,2018-12-21T05:00:00Z,,2018-12-21T17:11:04Z,,0,0,09000064839c0235
FDA-2017-E-6002-0004,FDA,FDA-2017-E-6002,Letter from the U.S. Patent and Trademark Office to FDA CDER,Other,Letter(s),2018-10-02T04:00:00Z,2018,10,2018-10-02T04:00:00Z,,2018-10-02T13:45:24Z,,0,0,090000648378b5ab