documents: FDA-2012-D-0880-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0880-0001 FDA FDA-2012-D-0880 Draft Guidances for Industry: Generic Drug User Fee Amendments of 2012, Questions and Answers Notice Notice of Availability 2012-08-27T04:00:00Z 2012 8 2012-08-27T04:00:00Z 2012-10-27T03:59:59Z 2012-10-02T02:01:15Z 2012-20944 0 0 09000064810f2477

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