documents: FDA-2012-D-0880-0021

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0880-0021 FDA FDA-2012-D-0880 Generic Drug User Fee Amendments of 2012: Questions and Answers Related to Self-Identification of Facilities, Review of Generic Drug Submissions, and Inspections and Compliance; Guidance for Industry; Availability Notice Notice of Availability 2017-07-26T04:00:00Z 2017 7 2017-07-26T04:00:00Z   2017-07-26T13:59:13Z 2017-15654 0 0 090000648296a012

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