documents: FDA-2012-D-0880-0020

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0880-0020 FDA FDA-2012-D-0880 Final Guidance for Industry Generic Drug User Fee Amendments of 2012 - Questions and Answers Related t User Fee Assessments Other Guidance 2016-12-14T05:00:00Z 2016 12 2016-12-14T05:00:00Z   2024-11-07T23:53:21Z   1 0 0900006482409ef4

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