documents: FDA-2012-D-0880-0007

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

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

This data as json

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0880-0007 FDA FDA-2012-D-0880 Draft Guidance for Industry on Generic Drug User Fee Amendments of 2012: Questions and Answers (Revision 1) Other Guidance 2013-09-10T04:00:00Z 2013 9 2013-09-10T04:00:00Z   2024-11-07T22:57:45Z   1 0 09000064813eca54

Links from other tables