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documents: FDA-1999-D-1301-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1999-D-1301-0001 FDA FDA-1999-D-1301 Guidance for Industry: Information Request & Discipline Review Letters Under the Prescription Drug User Fee Act Notice Guidance 2001-11-20T05:00:00Z 2001 11 2001-11-20T05:00:00Z   2025-06-17T21:52:51Z   1 0 09000064804da900

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