documents: FDA-2013-N-0500-0142

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2013-N-0500-0142 FDA FDA-2013-N-0500 02- Reference 01- Draft guidance for industry, “Updating ANDA Labeling After the Marketing Application for the Reference Listed Drug Has Been Withdrawn,” Supporting & Related Material Background Material 2018-12-14T05:00:00Z 2018 12     2018-12-14T15:13:06Z   0 0 09000064839949a3

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