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withdrawn,object_id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-2011-N-0915-0007,FDA,FDA-2011-N-0915,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application,Notice,60 Day Proposed Information Collection,2018-08-15T04:00:00Z,2018,8,2018-08-15T04:00:00Z,2018-10-16T03:59:59Z,2018-10-17T01:01:01Z,2018-17526,0,0,090000648362232f