documents: FDA-2012-D-0880-0006

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0880-0006 FDA FDA-2012-D-0880 Draft Guidance for Industry on Generic Drug User Fee Amendments of 2012: Questions and Answers (Revision 1); Availability Notice Notice of Availability 2013-09-10T04:00:00Z 2013 9 2013-09-10T04:00:00Z 2013-11-27T04:59:59Z 2016-11-18T14:44:33Z 2013-21891 0 0 09000064813ebe4c

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