documents: FDA-2017-D-6752-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-D-6752-0001 FDA FDA-2017-D-6752 Information Requests and Discipline Review Letters Under the Generic Drug User Fee Amendments; Draft Guidance for Industry; Availability Notice Notice of Availability 2017-12-18T05:00:00Z 2017 12 2017-12-18T05:00:00Z 2018-02-17T04:59:59Z 2018-02-17T02:02:50Z 2017-27124 0 0 0900006482d30211

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