documents: FDA-2009-D-0095-0015

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2009-D-0095-0015 FDA FDA-2009-D-0095 Clinical Pharmacology Section of Labeling for Human Prescription Drug and Biological Products—Content and Format; Guidance for Industry; Availability Notice Notice of Availability 2016-12-05T05:00:00Z 2016 12 2016-12-05T05:00:00Z   2016-12-05T16:25:46Z 2016-29125 0 0 09000064823deeb0

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