documents: FDA-2012-D-0880-0023

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0880-0023 FDA FDA-2012-D-0880 Assessing User Fees Under the Generic Drug User Fee Amendments of 2017; Draft Guidance for Industry; Availability Notice Notice of Availability 2017-10-30T04:00:00Z 2017 10 2017-10-30T04:00:00Z 2017-12-30T04:59:59Z 2017-12-29T02:00:42Z 2017-23526 0 0 0900006482c21d18

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