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Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

7 rows where docket_id = "FDA-2007-D-0429" and posted_year = 2008 sorted by posted_date descending

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Suggested facets: subtype, posted_date, posted_month, posted_date (date), comment_start_date (date), last_modified (date)

document_type 3

  • Supporting & Related Material 3
  • Notice 2
  • Other 2

posted_year 1

  • 2008 · 7 ✖

agency_id 1

  • FDA 7
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2007-D-0429-0014 FDA None FDA-2007-D-0429 Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Revision 1; Availability Notice Notice of Availability 2008-12-11T05:00:00Z 2008 12 2008-12-11T05:00:00Z   2019-08-20T11:52:24Z E8-29301 0 0 09000064807d7084
FDA-2007-D-0429-0015 FDA None 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
FDA-2007-D-0429-0012 FDA None FDA-2007-D-0429 The Honorable Orrin G. Hatch to the Assistant Commissioner for Policy, FDA - Letter Other LET-Letter 2008-06-17T04:00:00Z 2008 6 2008-06-17T04:00:00Z   2008-06-17T14:38:14Z   0 0 090000648062ac2d
FDA-2007-D-0429-0003 FDA None FDA-2007-D-0429 Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability Notice Notice of Availability 2008-06-16T04:00:00Z 2008 6 2008-06-16T04:00:00Z   2015-07-07T11:49:55Z 07–6267 0 0 09000064806294d9
FDA-2007-D-0429-0004 FDA None FDA-2007-D-0429 Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Draft Guidance Document Other Guidance 2008-06-16T04:00:00Z 2008 6 2008-01-02T19:57:32Z   2019-08-20T11:51:45Z   0 0 0900006480629527
FDA-2007-D-0429-0001 FDA None FDA-2007-D-0429 NO DOCUMENT POSTED - See FDA-2007-D-0429-0003 Supporting & Related Material BKG- Background Material (internal references) 2008-01-02T05:00:00Z 2008 1     2008-06-17T00:41:15Z   0 0 090000648042dc0a
FDA-2007-D-0429-0002 FDA None FDA-2007-D-0429 NO DOCUMENT POSTED - See FDA-2007-D-0429-0004 Supporting & Related Material GDL-Guidance 2008-01-02T05:00:00Z 2008 1     2008-06-17T00:42:14Z   0 0 090000648042dc0d

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CREATE TABLE documents (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    docket_id TEXT REFERENCES dockets(id),
    title TEXT,
    document_type TEXT,
    subtype TEXT,
    posted_date TEXT,
    posted_year INTEGER,
    posted_month INTEGER,
    comment_start_date TEXT,
    comment_end_date TEXT,
    last_modified TEXT,
    fr_doc_num TEXT,
    open_for_comment INTEGER,
    withdrawn INTEGER,
    object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;
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