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withdrawn,object_id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-2003-N-0385-0001,FDA,FDA-2003-N-0385,FDA,Notice,NAD-Notice of Availability of Data,2006-12-28T05:00:00Z,2006,12,2006-12-28T05:00:00Z,2007-04-03T03:59:59Z,2008-04-12T01:03:44Z,,0,0,090000648049a462
FDA-2006-P-0074-0007,FDA,FDA-2006-P-0074,FDA,Notice,N-Notice,2006-12-26T05:00:00Z,2006,12,2006-12-22T05:00:00Z,,2008-04-11T23:17:41Z,,0,0,0900006480444652
FDA-2006-D-0032-0005,FDA,FDA-2006-D-0032,FDA,Notice,NAD-Notice of Availability of Data,2006-12-22T05:00:00Z,2006,12,2006-12-21T05:00:00Z,,2008-04-11T22:52:06Z,,0,0,09000064804420d6
FDA-2006-N-0042-0002,FDA,FDA-2006-N-0042,Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment (DUPLICATE),Notice,Notice of Final Rule,2006-12-22T05:00:00Z,2006,12,2006-12-22T05:00:00Z,,2025-07-09T00:26:29Z,E6-21952,0,0,09000064804428d5
FDA-2006-N-0042-0001,FDA,FDA-2006-N-0042,Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment,Notice,Notice of Final Rule,2006-12-22T05:00:00Z,2006,12,2006-12-22T05:00:00Z,,2025-07-09T00:24:56Z,E6-21952,0,0,09000064804428d6
FDA-2005-D-0027-0004,FDA,FDA-2005-D-0027,FDA,Notice,NAD-Notice of Availability of Data,2006-12-21T05:00:00Z,2006,12,2006-12-20T05:00:00Z,,2008-04-11T23:46:25Z,,0,0,090000648043e843
FDA-2003-D-0030-0012,FDA,FDA-2003-D-0030,FDA,Notice,N-Notice,2006-12-20T05:00:00Z,2006,12,,,2008-04-12T00:54:03Z,,0,0,090000648048154e
FDA-2006-N-0420-0002,FDA,FDA-2006-N-0420,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications,Notice,General Notice,2006-12-20T05:00:00Z,2006,12,2006-12-20T05:00:00Z,2007-01-20T04:59:59Z,2025-06-18T22:33:57Z,E6-21636,0,0,09000064804617a1
FDA-2006-N-0046-0005,FDA,FDA-2006-N-0046,FDA,Notice,N-Notice,2006-12-20T05:00:00Z,2006,12,2006-12-19T05:00:00Z,,2008-04-11T23:09:21Z,,0,0,0900006480443f99
FDA-2003-N-0049-0025,FDA,FDA-2003-N-0049,FDA,Notice,NFR-Notice of Final Rule,2006-12-19T05:00:00Z,2006,12,2006-12-18T05:00:00Z,,2008-04-12T00:58:18Z,,0,0,0900006480481999
FDA-2006-D-0158-0009,FDA,FDA-2006-D-0158,FDA,Notice,N-Notice,2006-12-18T05:00:00Z,2006,12,2006-12-15T05:00:00Z,,2008-04-11T23:03:17Z,,0,0,0900006480450675
FDA-2006-N-0498-0002,FDA,FDA-2006-N-0498,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Experimental Study of Possible Footnotes and Cueing Schemes to Help Consumers Interpret Quantitative Trans Fat Disclosure on the Nutrition Facts Panel,Notice,General Notice,2006-12-17T05:00:00Z,2006,12,2006-12-18T05:00:00Z,2006-12-19T04:59:59Z,2025-05-19T21:37:55Z,E6-21486,0,0,0900006480463888
FDA-2006-N-0370-0002,FDA,FDA-2006-N-0370,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Registration of Food Facilities Under the Public Health Security and Bloterrorism Preparedness and Response Act of 2002,Notice,General Notice,2006-12-15T05:00:00Z,2006,12,2006-12-15T05:00:00Z,2007-01-17T04:59:59Z,2025-06-17T21:38:04Z,E6-21375,0,0,090000648045fe30
FDA-2006-N-0483-0001,FDA,FDA-2006-N-0483,"International Drug Scheduling; Convention on Psychotropic Substances; Single Convention on Narcotic Drugs; World Health Organization Scheduling Recommendations for Dronabinol and its Stereolsomers, and Oripavine",Notice,General Notice,2006-12-15T05:00:00Z,2006,12,2006-12-14T05:00:00Z,2007-01-17T04:59:59Z,2025-07-09T00:08:54Z,E6-21318,0,0,0900006480463157
FDA-2006-N-0234-0001,FDA,FDA-2006-N-0234,Drug Products Containing Quinine; Enforcement Action Dates,Notice,General Notice,2006-12-15T05:00:00Z,2006,12,2006-12-15T05:00:00Z,,2025-07-09T00:02:25Z,06-9713,0,0,09000064804568dc
FDA-2006-N-0253-0002,FDA,FDA-2006-N-0253,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Proposed Experimental Study of Trans Fat Claims on Foods,Notice,General Notice,2006-12-14T05:00:00Z,2006,12,2006-12-15T05:00:00Z,2006-12-15T04:59:59Z,2025-05-20T15:12:37Z,E6-21317,0,0,090000648045765f
FDA-2006-N-0419-0002,FDA,FDA-2006-N-0419,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Postmarket Surveillance,Notice,General Notice,2006-12-13T05:00:00Z,2006,12,2006-12-13T05:00:00Z,2007-01-13T04:59:59Z,2025-07-01T19:21:35Z,E6-21167,0,0,090000648046174a
FDA-1998-P-0086-0009,FDA,FDA-1998-P-0086,"Notice of Final Rule re Permit the label statement of ""Supplement Facts""",Notice,Notice of Final Rule,2006-12-13T05:00:00Z,2006,12,2006-12-12T05:00:00Z,,2015-12-07T13:50:33Z,,0,0,090000648058516b
FDA-2006-N-0246-0002,FDA,FDA-2006-N-0246,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format,Notice,General Notice,2006-12-12T05:00:00Z,2006,12,2006-12-13T05:00:00Z,2007-01-13T04:59:59Z,2025-05-22T16:22:18Z,E6-21132,0,0,09000064804572fc
FDA-2006-N-0306-0002,FDA,FDA-2006-N-0306,Withdrawal of Federal Register Notice,Notice,Withdrawal,2006-12-07T05:00:00Z,2006,12,2006-12-07T05:00:00Z,,2025-07-02T23:41:28Z,E6-20705,0,0,090000648045c593
FDA-2005-N-0294-0008,FDA,FDA-2005-N-0294,Color Additive Certification; Increase in Fees for Certification Services,Notice,Extension of Comment Period,2006-12-07T05:00:00Z,2006,12,2006-12-07T05:00:00Z,2007-02-06T04:59:59Z,2025-06-16T22:36:41Z,,0,0,0900006480446aa5
FDA-2006-N-0183-0002,FDA,FDA-2006-N-0183,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Establishing and Maintaining a List of United States Dairy Product Manufacturers/ Processors With Interest in Exporting to Chile,Notice,General Notice,2006-12-07T05:00:00Z,2006,12,2006-12-07T05:00:00Z,2007-01-09T04:59:59Z,2025-06-19T00:02:22Z,E6-20704,0,0,0900006480450db6
FDA-2006-N-0169-0001,FDA,FDA-2006-N-0169,Use of Ozone-Depleting Substances; Removal of Essential Use Designations; Companion Document to Direct Final Rule,Notice,NPR-Notice of Proposed Rule-Making,2006-12-07T05:00:00Z,2006,12,2006-12-07T05:00:00Z,2007-02-21T04:59:59Z,2025-07-01T22:39:04Z,E6-20796,0,0,0900006480450904
FDA-2006-N-0169-0002,FDA,FDA-2006-N-0169,Use of Ozone-Depleting Substances; Removal of Essential Use Designations,Notice,Notice of Final Rule,2006-12-07T05:00:00Z,2006,12,2006-12-07T05:00:00Z,2007-02-21T04:59:59Z,2025-07-01T22:42:39Z,E6-20797,0,0,0900006480450907
FDA-2006-N-0185-0001,FDA,FDA-2006-N-0185,Agency Information Collection Activities; Proposed Collection; Comment Request; Substances Prohibited from Use in Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed,Notice,General Notice,2006-12-04T05:00:00Z,2006,12,2006-12-04T05:00:00Z,2007-02-03T04:59:59Z,2025-07-08T23:31:41Z,E6-20476,0,0,0900006480450dd7
FDA-2006-N-0243-0001,FDA,FDA-2006-N-0243,Agency Information Collection Activities; Proposed Collection; Comment Request; Human Tissue Intended for Transplantation,Notice,General Notice,2006-12-04T05:00:00Z,2006,12,2006-12-04T05:00:00Z,2007-02-03T04:59:59Z,2025-07-08T23:47:27Z,E6-20477,0,0,0900006480457165
FDA-2005-N-0349-0002,FDA,FDA-2005-N-0349,Agency In formation Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Cosmetic Labeling Regulations,Notice,30 Day Proposed Information Collection,2006-12-04T05:00:00Z,2006,12,2006-12-01T05:00:00Z,,2025-10-21T18:01:53Z,E6-20478,0,0,0900006480449f95
FDA-2006-N-0109-0002,FDA,FDA-2006-N-0109,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Food Labeling; Notification Procedures for Statements on Dietary Supplements,Notice,General Notice,2006-12-01T05:00:00Z,2006,12,2006-12-01T05:00:00Z,2007-01-03T04:59:59Z,2025-06-20T16:04:44Z,E6-20307,0,0,0900006480450094
FDA-2006-D-0357-0004,FDA,FDA-2006-D-0357,FDA,Notice,NEC-Notice of Extension,2006-11-29T05:00:00Z,2006,11,2006-11-27T05:00:00Z,2007-03-06T04:59:59Z,2008-04-11T23:06:48Z,,0,0,090000648045f784
FDA-2006-D-0233-0004,FDA,FDA-2006-D-0233,FDA,Notice,NEC-Notice of Extension,2006-11-29T05:00:00Z,2006,11,2006-11-27T05:00:00Z,2007-03-06T04:59:59Z,2008-04-11T23:06:24Z,,0,0,09000064804565b8
FDA-2005-N-0465-0005,FDA,FDA-2005-N-0465,"Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Experimental Study of Qualified Health Claims: Consumer Inferences About Monounsaturated Fatty Acids From Olive Oil, EPA and Omega-3 Fatty Acids, and Green Tea",Notice,Notice of Approval,2006-11-29T05:00:00Z,2006,11,2006-11-28T05:00:00Z,,2025-10-23T22:50:41Z,E6-20200,0,0,0900006480450db4
FDA-2006-D-0233-0005,FDA,FDA-2006-D-0233,FDA,Notice,NEC-Notice of Extension,2006-11-29T05:00:00Z,2006,11,2006-11-27T05:00:00Z,2007-03-06T04:59:59Z,2008-04-11T23:06:27Z,,0,0,09000064804565b9
FDA-2006-N-0104-0001,FDA,FDA-2006-N-0104,FDA,Notice,NM-Notice of Meeting,2006-11-29T05:00:00Z,2006,11,2006-11-27T05:00:00Z,2007-04-13T03:59:59Z,2008-04-11T23:09:30Z,,0,0,090000648044f494
FDA-2005-D-0444-0004,FDA,FDA-2005-D-0444,FDA,Notice,NAD-Notice of Availability of Data,2006-11-29T05:00:00Z,2006,11,2006-11-27T05:00:00Z,,2008-04-11T23:47:35Z,,0,0,09000064804505cc
FDA-2006-N-0247-0001,FDA,FDA-2006-N-0247,Training Program for Regulatory Project Managers; Information Available to Industry,Notice,General Notice,2006-11-29T05:00:00Z,2006,11,2006-11-28T05:00:00Z,2007-01-30T04:59:59Z,2025-07-08T23:22:13Z,E6-20041,0,0,090000648045730d
FDA-2005-D-0084-0016,FDA,FDA-2005-D-0084,FDA,Notice,NAD-Notice of Availability of Data,2006-11-24T05:00:00Z,2006,11,2006-11-22T05:00:00Z,,2008-04-11T23:46:31Z,,0,0,090000648043f477
FDA-2006-N-0106-0001,FDA,FDA-2006-N-0106,Food Defense Workshop; Public Workshop,Notice,Meeting,2006-11-24T05:00:00Z,2006,11,2006-11-24T05:00:00Z,,2025-07-08T20:51:03Z,E6-19886,0,0,090000648044f5fd
FDA-2006-D-0475-0001,FDA,FDA-2006-D-0475,FDA,Notice,NAD-Notice of Availability of Data,2006-11-24T05:00:00Z,2006,11,2006-11-22T05:00:00Z,,2008-04-11T23:07:12Z,,0,0,0900006480462ec9
FDA-2006-D-0167-0001,FDA,FDA-2006-D-0167,FDA,Notice,NAD-Notice of Availability of Data,2006-11-21T05:00:00Z,2006,11,2006-11-21T05:00:00Z,2007-01-23T04:59:59Z,2008-04-11T23:03:22Z,,0,0,0900006480450814
FDA-2004-D-0124-0004,FDA,FDA-2004-D-0124,FDA,Notice,NAD-Notice of Availability of Data,2006-11-21T05:00:00Z,2006,11,2006-11-17T05:00:00Z,2007-11-20T04:59:59Z,2008-04-12T00:34:43Z,,0,0,090000648046fc8b
FDA-2006-N-0107-0001,FDA,FDA-2006-N-0107,FDA,Notice,NHC-Notice of Hearing Before Commissioner,2006-11-21T05:00:00Z,2006,11,2006-11-15T05:00:00Z,2006-12-09T04:59:59Z,2008-04-11T23:09:35Z,,0,0,090000648044f679
FDA-2006-D-0160-0007,FDA,FDA-2006-D-0160,FDA,Notice,NAD-Notice of Availability of Data,2006-11-15T05:00:00Z,2006,11,2006-11-14T05:00:00Z,2007-11-15T04:59:59Z,2008-04-11T23:03:21Z,,0,0,09000064804506c5
FDA-2006-N-0236-0001,FDA,FDA-2006-N-0236,FDA,Notice,NM-Notice of Meeting,2006-11-15T05:00:00Z,2006,11,2006-11-14T05:00:00Z,2006-12-02T04:59:59Z,2008-04-11T23:10:13Z,,0,0,0900006480456a21
FDA-1988-N-0003-0006,FDA,FDA-1988-N-0003,FDA,Notice,N-Notice,2006-11-15T05:00:00Z,2006,11,2006-11-14T05:00:00Z,,2008-05-30T22:53:21Z,,0,0,09000064804752dd
FDA-2006-N-0250-0001,FDA,FDA-2006-N-0250,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Food Additive Petitions,Notice,General Notice,2006-11-15T05:00:00Z,2006,11,2006-11-15T05:00:00Z,2006-12-16T04:59:59Z,2025-06-30T16:19:05Z,E6-19201,0,0,09000064804574ad
FDA-2006-N-0249-0001,FDA,FDA-2006-N-0249,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602),Notice,General Notice,2006-11-15T05:00:00Z,2006,11,2006-11-15T05:00:00Z,2006-12-16T04:59:59Z,2025-06-30T16:06:21Z,E6-19285,0,0,090000648045741e
FDA-2006-N-0252-0001,FDA,FDA-2006-N-0252,Agency Information Collection Activities; Proposed Collection; Comment Request; Agreement for Shipment of Devices for Sterilization,Notice,General Notice,2006-11-15T05:00:00Z,2006,11,2006-11-15T05:00:00Z,2007-01-17T04:59:59Z,2025-07-08T20:13:41Z,E6-19283,0,0,09000064804575a4
FDA-1992-N-0056-0018,FDA,FDA-1992-N-0056,Notice re Prescription Drug Marketing Act Pedigree Requirements under 21 CFR Part 203 Compliance Policy Guide and Guidance for Industry: Prescription Drug Marketing Act Pedigree Requirements Questions and Answers; Notice of Availability,Notice,General Notice,2006-11-15T05:00:00Z,2006,11,2006-11-14T05:00:00Z,,2016-11-08T14:36:00Z,,0,0,090000648052c00a
FDA-2006-D-0230-0001,FDA,FDA-2006-D-0230,FDA,Notice,NAD-Notice of Availability of Data,2006-11-14T05:00:00Z,2006,11,2006-11-13T05:00:00Z,2007-01-30T04:59:59Z,2008-04-11T23:06:12Z,,0,0,0900006480456323
FDA-2006-D-0302-0001,FDA,FDA-2006-D-0302,FDA,Notice,NAD-Notice of Availability of Data,2006-11-14T05:00:00Z,2006,11,2006-11-13T05:00:00Z,2007-01-17T04:59:59Z,2008-04-11T23:06:39Z,,0,0,0900006480459166
FDA-2006-N-0426-0001,FDA,FDA-2006-N-0426,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medicated Feed Mill License Application,Notice,General Notice,2006-11-14T05:00:00Z,2006,11,2006-11-14T05:00:00Z,2006-12-15T04:59:59Z,2025-06-30T17:01:19Z,E6-19152,0,0,0900006480461a11
FDA-1992-N-0056-0017,FDA,FDA-1992-N-0056,Notice of Final Rule re Distribution of Blood Derivatives by Registered Blood Establishments Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Delay of Applicability Date,Notice,Notice of Final Rule,2006-11-13T05:00:00Z,2006,11,2006-11-09T05:00:00Z,,2016-11-08T14:39:45Z,,0,0,090000648052c009
FDA-2006-N-0184-0002,FDA,FDA-2006-N-0184,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Reagents for Detection of Specific Novel Influenza A Viruses,Notice,General Notice,2006-11-09T05:00:00Z,2006,11,2006-11-09T05:00:00Z,2006-12-12T04:59:59Z,2025-06-17T20:15:22Z,E6-19045,0,0,0900006480450dce
FDA-2006-N-0251-0001,FDA,FDA-2006-N-0251,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit a Notice of Final Disposition of Animals Not Intended for Immediate Slaughter,Notice,General Notice,2006-11-09T05:00:00Z,2006,11,2006-11-09T05:00:00Z,2007-01-09T04:59:59Z,2025-07-08T17:02:13Z,E6-19044,0,0,0900006480457517
FDA-2006-N-0181-0001,FDA,FDA-2006-N-0181,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit Information to the Center for Veterinary Medicine,Notice,General Notice,2006-11-08T05:00:00Z,2006,11,2006-11-08T05:00:00Z,2007-01-09T04:59:59Z,2025-07-08T16:48:07Z,E6-18901,0,0,0900006480450d8a
FDA-2006-N-0114-0002,FDA,FDA-2006-N-0114,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance For Industry on How to Use E-Mail to Submit a Request for a Meeting or Teleconference to the Office Of New Animal Drug Evaluation,Notice,General Notice,2006-11-08T05:00:00Z,2006,11,2006-11-08T05:00:00Z,2007-01-09T04:59:59Z,2025-07-08T17:51:42Z,E6-18911,0,0,09000064804500ea
FDA-2006-N-0497-0001,FDA,FDA-2006-N-0497,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How To Use E-Mail To Submit A Study Protocol,Notice,General Notice,2006-11-08T05:00:00Z,2006,11,2006-11-08T05:00:00Z,2007-01-09T04:59:59Z,2025-07-08T18:57:50Z,E6-18908,0,0,0900006480463868
FDA-2006-N-0182-0001,FDA,FDA-2006-N-0182,Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit a Notice of Intent to Slaughter for Human Food Purposes,Notice,General Notice,2006-11-08T05:00:00Z,2006,11,2006-11-08T05:00:00Z,2007-01-09T04:59:59Z,2025-07-08T18:14:54Z,E6-18896,0,0,0900006480450d98
FDA-2006-N-0494-0002,FDA,FDA-2006-N-0494,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002,Notice,General Notice,2006-11-03T05:00:00Z,2006,11,2006-11-03T05:00:00Z,2006-12-05T04:59:59Z,2025-06-21T00:17:07Z,E6-18603,0,0,090000648046377e
FDA-2006-N-0179-0001,FDA,FDA-2006-N-0179,Agency Information Collection Activities; Proposed Collection; Comment Request; Premarket Notification,Notice,General Notice,2006-11-03T05:00:00Z,2006,11,2006-11-03T05:00:00Z,2007-01-03T04:59:59Z,2025-07-02T23:26:15Z,E6-18553,0,0,0900006480450c0a
FDA-2004-N-0451-0010,FDA,FDA-2004-N-0451,"Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 016",Notice,Notice of Publication,2006-11-03T05:00:00Z,2006,11,2006-11-03T05:00:00Z,,2025-04-16T16:00:40Z,E6--18604,0,0,090000648047543b
FDA-2006-N-0228-0001,FDA,FDA-2006-N-0228,Agency Information Collection Activities; Proposed Collection; Comment Request; Reporting and Recordkeeping Requirements and Availability of Sample Electronic Products for Manufacturers and Distributors of Electronic Products,Notice,General Notice,2006-11-03T05:00:00Z,2006,11,2006-11-03T05:00:00Z,2007-01-03T04:59:59Z,2025-07-02T23:46:12Z,E6-18559,0,0,09000064804562d9
FDA-2006-N-0044-0002,FDA,FDA-2006-N-0044,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Medical Device User Fee Cover Sheet,Notice,General Notice,2006-11-03T05:00:00Z,2006,11,2006-11-03T05:00:00Z,2006-12-05T04:59:59Z,2025-06-18T23:34:36Z,E6-18557,0,0,09000064804429c6
FDA-2005-D-0227-0004,FDA,FDA-2005-D-0227,"Questions and Answers Regarding Food Allergens, including the Food Allergen Labeling and Consumer Protection Act of 2004; Availability (Edition 4)",Notice,NAD-Notice of Availability of Data,2006-11-02T05:00:00Z,2006,11,2006-11-01T05:00:00Z,2007-11-02T03:59:59Z,2008-07-09T14:42:08Z,,0,0,090000648044207c
FDA-2006-N-0180-0001,FDA,FDA-2006-N-0180,Agency Information Collection Activities; Proposed Collection; Comment Request; Substantial Evidence of Effectiveness of New Animal Drugs,Notice,General Notice,2006-11-02T05:00:00Z,2006,11,2006-11-02T05:00:00Z,2007-01-03T04:59:59Z,2025-07-03T01:10:23Z,E6-18432,0,0,0900006480450cb5
FDA-2003-D-0030-0011,FDA,FDA-2003-D-0030,FDA,Notice,NM-Notice of Meeting,2006-11-02T05:00:00Z,2006,11,2006-10-31T05:00:00Z,,2008-04-12T00:54:01Z,,0,0,0900006480481546
FDA-2006-N-0309-0001,FDA,FDA-2006-N-0309,"Agency Information Collection Activities; Proposed Collection; Comment Request; General Licensing Provisions: Biologics License Application, Changes to an Approved Application, Labeling, Revocation and Suspension, Postmarketing Studies Status Reports, and Forms FDA 356h and 2567",Notice,General Notice,2006-11-02T05:00:00Z,2006,11,2006-11-02T05:00:00Z,2007-01-03T04:59:59Z,2025-07-02T23:58:42Z,E6-18445,0,0,090000648045c6e8
FDA-2006-N-0306-0001,FDA,FDA-2006-N-0306,Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602),Notice,General Notice,2006-10-31T05:00:00Z,2006,10,2006-10-31T05:00:00Z,2007-01-03T04:59:59Z,2025-07-02T23:38:35Z,E6-18198,0,0,090000648045c57a
FDA-2006-N-0423-0003,FDA,FDA-2006-N-0423,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Infectious Disease Issues in Xenotransplantation,Notice,General Notice,2006-10-31T05:00:00Z,2006,10,2006-10-31T05:00:00Z,2006-12-01T04:59:59Z,2025-06-18T23:08:36Z,E6-18203,0,0,09000064804618c5
FDA-2006-N-0489-0001,FDA,FDA-2006-N-0489,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Investigational Device Exemptions Reports and Records,Notice,General Notice,2006-10-31T05:00:00Z,2006,10,2006-10-31T05:00:00Z,2006-12-01T04:59:59Z,2025-06-17T20:30:37Z,E6-18200,0,0,090000648046356b
FDA-2006-D-0356-0001,FDA,FDA-2006-D-0356,Draft Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Absorbable Hemostatic Device; Availability,Notice,NAD-Notice of Availability of Data,2006-10-31T05:00:00Z,2006,10,2006-10-30T05:00:00Z,2007-01-30T04:59:59Z,2008-10-10T21:42:17Z,,0,0,090000648045f6a0
FDA-2006-N-0417-0002,FDA,FDA-2006-N-0417,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Administrative Detention and Banned Medical Devices,Notice,General Notice,2006-10-31T05:00:00Z,2006,10,2006-10-31T05:00:00Z,2006-12-01T04:59:59Z,2025-06-18T21:59:00Z,E6-18190,0,0,0900006480461672
FDA-2006-N-0425-0001,FDA,FDA-2006-N-0425,Agency Information Collection Activities; Proposed Collection; Comment Request; Biological Products: Reporting of Biological Product Deviations in Manufacturing; Forms FDA 3486 and 3486A,Notice,General Notice,2006-10-31T05:00:00Z,2006,10,2006-10-31T05:00:00Z,2007-01-03T04:59:59Z,2025-07-02T16:03:19Z,E6-18313,0,0,0900006480461999
FDA-2004-D-0105-0009,FDA,FDA-2004-D-0105,FDA,Notice,NAD-Notice of Availability of Data,2006-10-30T05:00:00Z,2006,10,2006-10-27T04:00:00Z,2007-10-31T03:59:59Z,2008-04-12T00:34:18Z,,0,0,090000648046f5dc
FDA-2006-D-0297-0001,FDA,FDA-2006-D-0297,Draft Guidance for Industry: Blue Bird Medicated Feed Labels; Availability,Notice,NAD-Notice of Availability of Data,2006-10-30T05:00:00Z,2006,10,2006-10-27T04:00:00Z,2007-01-17T04:59:59Z,2008-11-22T01:00:29Z,,0,0,0900006480458df1
FDA-2006-N-0496-0001,FDA,FDA-2006-N-0496,Agency Information Collection Activities; Proposed Collection; Comment Request; Orphan Drugs,Notice,General Notice,2006-10-29T04:00:00Z,2006,10,2006-10-30T05:00:00Z,2006-12-30T04:59:59Z,2025-07-01T23:32:05Z,E6-18067,0,0,0900006480463820
FDA-2004-N-0054-0009,FDA,FDA-2004-N-0054,Agency Information Collection Activities; Announcement of Office of Management and Budget; Extension of Expiration Date for MedWatch (Food and Drug Administration Medical Products Reporting Program) Form,Notice,Notice of Extension,2006-10-26T04:00:00Z,2006,10,,,2025-06-05T19:12:02Z,E6-17907,0,0,090000648046e914
FDA-2006-D-0039-0001,FDA,FDA-2006-D-0039,FDA,Notice,NAD-Notice of Availability of Data,2006-10-26T04:00:00Z,2006,10,2006-10-26T04:00:00Z,2007-01-25T04:59:59Z,2008-04-11T22:52:12Z,,0,0,0900006480442261
FDA-2004-D-0299-0004,FDA,FDA-2004-D-0299,FDA,Notice,NAL-Notice of Approval,2006-10-25T04:00:00Z,2006,10,2006-10-23T04:00:00Z,,2008-04-12T00:35:41Z,,0,0,0900006480472d3c
FDA-2006-D-0229-0001,FDA,FDA-2006-D-0229,FDA,Notice,NAD-Notice of Availability of Data,2006-10-25T04:00:00Z,2006,10,2006-10-23T04:00:00Z,2007-01-23T04:59:59Z,2008-04-11T23:06:11Z,,0,0,09000064804562e3
FDA-2006-D-0360-0001,FDA,FDA-2006-D-0360,FDA,Notice,NAD-Notice of Availability of Data,2006-10-25T04:00:00Z,2006,10,2006-10-23T04:00:00Z,2007-01-23T04:59:59Z,2008-04-11T23:06:52Z,,0,0,090000648045f966
FDA-2002-P-0226-0002,FDA,FDA-2002-P-0226,FDA Notice - Notice of Hearing Before Commissioner,Notice,NHC-Notice of Hearing Before Commissioner,2006-10-25T04:00:00Z,2006,10,2006-10-24T04:00:00Z,2007-01-06T04:59:59Z,2009-03-18T22:03:17Z,,0,0,090000648049746f
FDA-2006-F-0056-0001,FDA,FDA-2006-F-0056,Safe Foods Corporation; Filing of Food Additive Petition,Notice,Notice of Filing,2006-10-25T04:00:00Z,2006,10,2006-10-25T04:00:00Z,2006-11-25T04:59:59Z,2026-01-10T08:06:50Z,E6-17834,0,0,090000648044413b
FDA-2006-P-0074-0006,FDA,FDA-2006-P-0074,FDA,Notice,N-Notice,2006-10-25T04:00:00Z,2006,10,2006-10-23T04:00:00Z,2006-11-25T04:59:59Z,2008-04-11T23:17:40Z,,0,0,09000064804445cf
FDA-2006-N-0493-0003,FDA,FDA-2006-N-0493,"Agency Information Collection Activities; Announcement of Office of Management and Budget Approval;
Request for Samples and Protocols",Notice,Notice of Approval,2006-10-25T00:00:00Z,2006,10,2006-10-24T04:00:00Z,2006-10-25T03:59:59Z,2025-05-17T00:02:01Z,E6-17720,0,0,090000648046370a
FDA-2001-D-0008-0004,FDA,FDA-2001-D-0008,FDA,Notice,NAD-Notice of Availability of Data,2006-10-20T04:00:00Z,2006,10,2006-10-19T04:00:00Z,2007-10-20T03:59:59Z,2008-04-25T02:25:09Z,,0,0,09000064804b45d8
FDA-2001-D-0007-0003,FDA,FDA-2001-D-0007,FDA,Notice,NAD-Notice of Availability of Data,2006-10-20T04:00:00Z,2006,10,2006-10-19T04:00:00Z,2007-10-20T03:59:59Z,2008-04-25T01:57:38Z,,0,0,09000064804b443b
FDA-2004-D-0301-0006,FDA,FDA-2004-D-0301,"Guidance for Industry on Fixed Dose Combina.tions, Co-Packaged Drug
Products, and Single-Entity Versions of Previously Approved Antiretrovirals
for the Treatment of HIV; Availability",Notice,NAD-Notice of Availability of Data,2006-10-18T04:00:00Z,2006,10,2006-10-17T04:00:00Z,2007-10-19T03:59:59Z,2020-09-10T17:30:49Z,,0,0,0900006480472ddf
FDA-2006-N-0474-0002,FDA,FDA-2006-N-0474,Anne L. Burkovitz; Debarment Order,Notice,Notice of Final Rule,2006-10-17T00:00:00Z,2006,10,2006-10-17T04:00:00Z,2006-10-18T03:59:59Z,2025-05-16T23:20:47Z,E6-17178,1,0,0900006480462e7c
FDA-2006-N-0113-0002,FDA,FDA-2006-N-0113,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Interstate Shellfish Dealers Certificate,Notice,General Notice,2006-10-13T04:00:00Z,2006,10,2006-10-13T04:00:00Z,2006-11-14T04:59:59Z,2025-06-16T23:25:54Z,E6-16953,0,0,09000064804500df
FDA-1998-D-0019-0001,FDA,FDA-1998-D-0019,FDA,Notice,NAD-Notice of Availability of Data,2006-10-12T04:00:00Z,2006,10,2006-10-11T04:00:00Z,2007-10-12T03:59:59Z,2008-05-16T21:17:59Z,,0,0,0900006480563d59
FDA-2006-N-0307-0002,FDA,FDA-2006-N-0307,FDA,Notice,N-Notice,2006-10-12T00:00:00Z,2006,10,2006-10-11T00:00:00Z,2006-10-13T03:59:59Z,2025-05-07T01:19:39Z,71FR18338,0,0,090000648045c606
FDA-2004-E-0464-0006,FDA,FDA-2004-E-0464,Redetermination of Regulatory Review Period for Purposes of Patent Extension; BONIVA; Correction,Notice,Correction,2006-10-11T04:00:00Z,2006,10,2006-10-11T04:00:00Z,,2025-11-20T18:32:10Z,E6-16816,0,0,0900006480475801
FDA-2004-N-0189-0008,FDA,FDA-2004-N-0189,"RuleRecordkeeping Requirements for Human Food and Cosmetics Manufactured from Processed With, or Otherwise Containing Material form Cattle; Notice of Final",Notice,Notice of Final Rule,2006-10-11T04:00:00Z,2006,10,2006-10-10T04:00:00Z,,2015-06-01T15:44:18Z,,0,0,0900006480470948
FDA-2005-D-0023-0008,FDA,FDA-2005-D-0023,FDA,Notice,NAD-Notice of Availability of Data,2006-10-10T04:00:00Z,2006,10,2006-10-04T04:00:00Z,,2008-04-11T23:46:20Z,,0,0,090000648043e7b9
FDA-2006-E-0124-0005,FDA,FDA-2006-E-0124,Determination of Regulatory Review Period for Purposes of Patent Extension; DRAXXIN - Federal Register Notice,Notice,N-Notice,2006-10-03T04:00:00Z,2006,10,2006-09-29T04:00:00Z,2006-12-02T04:59:59Z,2008-05-30T16:45:01Z,,0,0,09000064804501b5
FDA-2006-N-0112-0002,FDA,FDA-2006-N-0112,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Proposed Collection; Comment Request; Guidance for Industry on Submitting and Reviewing Complete Responses to Clinical Holds,Notice,General Notice,2006-10-03T04:00:00Z,2006,10,2006-10-02T04:00:00Z,2006-11-02T04:59:59Z,2025-06-18T19:49:00Z,E6-16225,0,0,09000064804500d0
FDA-2006-N-0419-0001,FDA,FDA-2006-N-0419,Agency Information Collection Activities; Proposed Collection; Comment Request; Postmarket Surveillance,Notice,General Notice,2006-10-03T04:00:00Z,2006,10,2006-10-02T04:00:00Z,2006-12-02T04:59:59Z,2025-07-01T18:43:34Z,E6-16231,0,0,0900006480461738
FDA-2006-E-0378-0005,FDA,FDA-2006-E-0378,Determination of Regulatory Review Period for Purposes of Patent Extension; BYETTA,Notice,General Notice,2006-10-03T04:00:00Z,2006,10,2006-10-02T04:00:00Z,,2025-12-18T00:32:20Z,E6-16086,0,0,09000064804601b0
FDA-2006-N-0239-0002,FDA,FDA-2006-N-0239,Index of Legally Marketed Unapproved New Animal Drugs for Minor Species; Extension of Comment Period,Notice,Notice of Extension,2006-10-03T04:00:00Z,2006,10,2006-09-29T04:00:00Z,2006-12-21T04:59:59Z,2015-12-15T22:00:40Z,,0,0,0900006480456f27