documents: FDA-2007-D-0429-0015

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2007-D-0429-0015 FDA FDA-2007-D-0429 Guidance for Industry - Question and Answers regarding the labeling of nonprescription human drug products marketed without an approved application as reqired by the dietary supplement and nonprescription drug consumer protection act: revision 1 Supporting & Related Material Guidance 2008-12-11T05:00:00Z 2008 12     2015-07-07T11:58:17Z   0 0 09000064807d71ee

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