documents

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

5 rows where docket_id = "FDA-2006-E-0381" and posted_year = 2006 sorted by posted_date descending

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

document_type 2

posted_year 1

  • 2006 · 5 ✖

agency_id 1

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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2006-E-0381-0005 FDA Patent Extension Application for SYMLIN (pramlintide acetate), U.S. Patent No. 5,686,411 FDA-2006-E-0381 Determination of Regulatory Review Period for Purposes of Patent Extension; SYMLIN Notice General Notice 2006-06-19T04:00:00Z 2006 6 2006-06-16T04:00:00Z   2025-12-11T01:05:26Z E6-9414 0 0 090000648046034c
FDA-2006-E-0381-0003 FDA Patent Extension Application for SYMLIN (pramlintide acetate), U.S. Patent No. 5,686,411 FDA-2006-E-0381 Letter from U.S. Patent and Trademark Office to FDA CDER Other Letter(s) 2006-05-25T04:00:00Z 2006 5     2025-12-11T00:30:44Z   0 0 090000648046034a
FDA-2006-E-0381-0004 FDA Patent Extension Application for SYMLIN (pramlintide acetate), U.S. Patent No. 5,686,411 FDA-2006-E-0381 Letter from FDA CDER to U. S. Patent and Trademark Office Other Letter(s) 2006-05-25T04:00:00Z 2006 5     2025-12-11T00:32:17Z   0 0 090000648046034b
FDA-2006-E-0381-0002 FDA Patent Extension Application for SYMLIN (pramlintide acetate), U.S. Patent No. 5,686,411 FDA-2006-E-0381 Letter from FDA CDER to U.S. Patent and Trademark Office Other Letter(s) 2006-02-27T05:00:00Z 2006 2     2025-12-11T00:20:23Z   0 0 0900006480460349
FDA-2006-E-0381-0001 FDA Patent Extension Application for SYMLIN (pramlintide acetate), U.S. Patent No. 5,686,411 FDA-2006-E-0381 Letter from U.S. Patent and Trademark Office to FDA CDER Other Letter(s) 2006-01-12T05:00:00Z 2006 1     2025-12-11T00:18:22Z   0 0 090000648046032b

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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);