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documents: FDA-1999-N-0139-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-N-0139-0001 FDA FDA-1999-N-0139 Progestational Drug Products for Human Use; Requirements for Labeling Directed to the Patient Notice NPR-Notice of Proposed Rule-Making 1999-04-19T04:00:00Z 1999 4 1999-04-13T04:00:00Z 1999-07-13T03:59:59Z 2024-11-19T13:53:12Z 99-9146 0 0 09000064804aedfe

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