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

18 rows where agency_id = "FDA", document_type = "Proposed Rule" and posted_year = 2006 sorted by posted_date descending

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

posted_year 1

  • 2006 · 18 ✖

document_type 1

  • Proposed Rule · 18 ✖

agency_id 1

  • FDA · 18 ✖
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1977-N-0013-0001 FDA Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Use; Proposed Amendment of the Tentative Final Monograph; Required Warnings and Other Labeling - OPEN FDA-1977-N-0013 Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Proposed Amendment of the Tentative Final Monograph; Required Warnings and Other Labeling Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-12-19T05:00:00Z 2006 12 2006-12-19T05:00:00Z 2007-06-20T03:59:59Z 2019-03-23T23:59:29Z E6-21855 0 0 09000064805d7f3f
FDA-2006-N-0237-0001 FDA Charging for Investigational Drugs Treatment Use FDA-2006-N-0237 Notice of Proposed Rulemaking re Charging for Investigational Drugs Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-12-14T05:00:00Z 2006 12 2006-12-14T05:00:00Z 2007-03-21T03:59:59Z 2016-02-12T22:00:43Z   0 0 0900006480456b5d
FDA-2006-N-0238-0001 FDA Expanded Access to Investigational Drugs for Treatment Use FDA-2006-N-0238 Expanded Access to Investigational Drugs for Treatment Use Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-12-14T00:00:00Z 2006 12 2006-12-14T05:00:00Z 2007-03-15T03:59:59Z 2025-05-21T09:01:14Z 06-9684 0 0 0900006480456c8f
FDA-1998-N-0009-0001 FDA Definition and Option of Alternative Labeling Requirements for Convenience Size OTC Drug Packages FDA-1998-N-0009 Over-the-Counter Human Drugs; Labeling Requirements; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-12-12T05:00:00Z 2006 12 2006-12-11T05:00:00Z 2007-04-12T03:59:59Z 2019-10-10T13:24:46Z   0 0 0900006480558e9b
FDA-2006-N-0178-0001 FDA General & Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device FDA-2006-N-0178 General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device Proposed Rule NPR-Notice of Proposed Rule-Making 2006-10-31T05:00:00Z 2006 10 2006-10-30T05:00:00Z 2007-01-30T04:59:59Z 2008-07-07T18:20:13Z   0 0 0900006480450b90
FDA-2005-N-0464-0008 FDA Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs FDA-2005-N-0464 Notice of Extension re Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs; Public Meeting; Extension of Comment Period Proposed Rule Extension of Comment Period 2006-10-31T05:00:00Z 2006 10 2006-10-30T05:00:00Z 2007-01-27T04:59:59Z 2016-12-19T17:17:44Z   0 0 0900006480450c15
FDA-1978-N-0023-0005 FDA Skin Bleaching Drug Products- OPEN FDA-1978-N-0023 Skin Bleaching Drug Products For Over-the-Counter Human Use; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-29T04:00:00Z 2006 8 2006-08-28T04:00:00Z 2006-12-28T04:59:59Z 2019-09-26T13:15:35Z E6-14263 0 0 090000648055f1de
FDA-2005-N-0464-0002 FDA Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs FDA-2005-N-0464 Proposed rule on Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs (Pages 201-300) Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-23T04:00:00Z 2006 8 2006-08-23T04:00:00Z 2006-11-28T04:59:59Z 2017-08-15T14:33:55Z   0 0 0900006480450bee
FDA-2005-N-0464-0001 FDA Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs FDA-2005-N-0464 Proposed rule on Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs (Pages 301-319) Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-23T04:00:00Z 2006 8 2006-08-23T04:00:00Z 2006-11-28T04:59:59Z 2017-08-15T14:32:51Z   0 0 0900006480450bce
FDA-2005-N-0464-0003 FDA Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs FDA-2005-N-0464 Proposed rule on Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs (Pages 1-100) Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-23T04:00:00Z 2006 8 2006-08-23T04:00:00Z 2006-11-28T04:59:59Z 2017-08-15T14:35:39Z   0 0 0900006480450bf2
FDA-2005-N-0464-0004 FDA Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs FDA-2005-N-0464 Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs that are Regulated Under a Biologics License Application, and Animal Drugs (Pages 101-200) Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-23T04:00:00Z 2006 8 2006-08-23T04:00:00Z 2006-11-28T04:59:59Z 2016-03-14T19:19:42Z   0 0 0900006480450bf3
FDA-2006-N-0239-0001 FDA Index of Legally Marketed Unapproved New Animal Drugs for Minor Species FDA-2006-N-0239 Index of Legally Marketed Unapproved New Animal Drugs for Minor Species; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-08-22T04:00:00Z 2006 8 2006-08-21T04:00:00Z 2006-11-21T04:59:59Z 2015-12-15T22:00:50Z   0 0 0900006480456ecf
FDA-1995-N-0063-0010 FDA CGMPs for the Production of Infant Formula FDA-1995-N-0063 Current Good Manufacturing Practice, Quality Control Procedures, Quality Factors, Notification Requirements, and Records and Reports for the Production of Infant Formula; Reopening of the Comment Period Proposed Rule Reopening of Comment Period 2006-08-01T04:00:00Z 2006 8 2006-07-28T04:00:00Z 2006-09-16T03:59:59Z 2014-07-17T01:05:26Z   0 0 090000648056cbef
FDA-2006-N-0171-0001 FDA Blood Vessels Recovered with Organs and Intended for Use in Organ Transplantation - CLOSED FDA-2006-N-0171 Blood Vessels Recovered With Organs and Intended for Use in Organ Transplantation; Companion Document to Direct Final Rule; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-05-18T04:00:00Z 2006 5 2006-05-12T04:00:00Z 2006-07-27T03:59:59Z 2025-05-20T19:58:09Z 06-4370 0 0 0900006480450945
FDA-2005-N-0343-0001 FDA Medical Gas Containers and Closures; Current Good Manufacturing Practice Requirements FDA-2005-N-0343 Notice of Proposed Rule-Making re Medical Gas Containers and Closures; Current Good Manufacturing Practice Requirements Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-04-10T04:00:00Z 2006 4 2006-04-07T04:00:00Z 2006-07-11T03:59:59Z 2016-11-19T02:00:53Z   0 0 090000648044954b
FDA-2005-N-0345-0001 FDA Distribution of Blood Derivatives by Registered Blood Establishments that Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements and Administrative Procedures (Section 610 Review) FDA-2005-N-0345 Distribution of Blood Derivatives by Registered Blood Establishments that Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements and Administrative Procedures; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-02-02T05:00:00Z 2006 2 2006-01-31T05:00:00Z 2006-05-03T03:59:59Z 2025-10-16T22:13:32Z E6-1225 0 0 0900006480449864
FDA-1998-P-0032-0001 FDA Prohibition of Cochineal Extract and Carmine Color Additives - CLOSED FDA-1998-P-0032 Listing of Color Additives Exempt From Certification; Food, Drug, and Cosmetic Labeling: Cochineal Extract and Carmine Declaration; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-01-30T05:00:00Z 2006 1 2006-01-30T05:00:00Z 2006-05-02T03:59:59Z 2016-03-11T17:00:14Z   0 0 09000064805651d4
FDA-2005-N-0170-0001 FDA Current Good Manufacturing Practice Regulation and Investigational New Drugs FDA-2005-N-0170 Current Good Manufacturing Practice Regulation and Investigational New Drugs; Companion Document to Direct Final Rule; Proposed Rule Proposed Rule Notice of Proposed Rulemaking (NPRM) 2006-01-17T05:00:00Z 2006 1 2006-01-12T05:00:00Z 2006-04-04T03:59:59Z 2015-11-19T02:30:48Z   0 0 0900006480440c01

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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);