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withdrawn,object_id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-2014-N-1210-0001,FDA,FDA-2014-N-1210,Neurological Devices; Reclassification of Electroconvulsive Therapy Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older Who Are Treatment Resistant or Require a Rapid Response; Effective Date of Requirement for Premarket Approval for Electroconvulsive Therapy for Certain Specified Intended Uses,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-12-29T05:00:00Z,2015,12,2015-12-29T05:00:00Z,2016-03-29T03:59:59Z,2019-01-14T20:50:27Z,2015-32592,0,0,0900006481dd79bf
FDA-2015-D-3719-0002,FDA,FDA-2015-D-3719,"Draft Guidances Relating to the Regulation of Human Cells, Tissues, or
Cellular or Tissue-Based Products; Public Hearing; Request for Comments; Correction",Proposed Rule,Notice of Hearing,2015-12-29T05:00:00Z,2015,12,2015-12-29T05:00:00Z,,2015-12-29T15:40:51Z,2015-32686,0,0,0900006481dd7b11
FDA-2014-N-1207-1827,FDA,FDA-2014-N-1207,"Use of the Term ‘‘Natural’’ in the Labeling of Human Food Products;
Request for Information and Comments; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2015-12-28T05:00:00Z,2015,12,2015-12-28T05:00:00Z,2016-05-11T03:59:59Z,2016-05-25T18:00:36Z,2015-32471,0,0,0900006481dd3c6d
FDA-2015-N-1260-0001,FDA,FDA-2015-N-1260,Fixed-Combination and Co-Packaged Drugs: Applications for Approval and Combinations of Active Ingredients Under Consideration for Inclusion in an Over-the-Counter Monograph,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-12-23T05:00:00Z,2015,12,2015-12-23T05:00:00Z,2016-05-19T03:59:59Z,2016-05-12T11:47:00Z,2015-32246,0,0,0900006481dc97c5
FDA-2015-N-1765-0001,FDA,FDA-2015-N-1765,"General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use
of Sunlamp Products",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-12-22T05:00:00Z,2015,12,2015-12-22T05:00:00Z,2016-03-22T03:59:59Z,2016-10-20T01:03:49Z,2015-32024,0,0,0900006481dc1394
FDA-1998-N-0880-0004,FDA,FDA-1998-N-0880,Sunlamp Products; Proposed Amendment to Performance Standard,Proposed Rule,Amendment,2015-12-22T05:00:00Z,2015,12,2015-12-22T05:00:00Z,2016-03-22T03:59:59Z,2016-12-16T02:00:42Z,2015-32023,0,0,0900006481dc147f
FDA-1998-N-0088-0004,FDA,FDA-1998-N-0088,Exports: Notification and Recordkeeping Requirements; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-12-11T05:00:00Z,2015,12,2015-12-11T05:00:00Z,1999-06-17T03:59:59Z,2015-12-11T22:00:33Z,,0,0,0900006480585da2
FDA-1998-N-0088-0014,FDA,FDA-1998-N-0088,Exports: Notification and Recordkeeping Requirements; Extension of Comment Period; Proposed rule; Extension of Comment Period.,Proposed Rule,Extension of Comment Period,2015-12-11T05:00:00Z,2015,12,2015-12-11T05:00:00Z,1999-07-17T03:59:59Z,2015-12-14T22:00:39Z,,0,0,0900006480585def
FDA-2015-N-2002-0008,FDA,FDA-2015-N-2002,"Clarification of When Products Made or Derived From Tobacco Are
Regulated as Drugs, Devices, or Combination Products; Amendments
to Regulations Regarding ‘‘Intended Uses’’; Reopening of the Comment
Period",Proposed Rule,Reopening of Comment Period,2015-11-30T05:00:00Z,2015,11,2015-11-30T05:00:00Z,2015-12-31T04:59:59Z,2015-12-31T22:00:26Z,2015-30271,0,0,0900006481d7964a
FDA-2015-F-4282-0001,FDA,FDA-2015-F-4282,BASF Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2015-11-24T05:00:00Z,2015,11,2015-11-24T05:00:00Z,,2015-11-24T17:19:20Z,2015-29832,0,0,0900006481d6d344
FDA-1998-N-1169-0001,FDA,FDA-1998-N-1169,Notice of Proposed Rulemaking re Requirements for Testing Human Blood Donors for Evidence of Infection Due to Communicable Disease Agens,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-18T05:00:00Z,2015,11,1999-08-19T04:00:00Z,1999-11-18T04:59:59Z,2015-11-20T15:09:08Z,,0,0,09000064805a3304
FDA-2014-N-1021-0001,FDA,FDA-2014-N-1021,Food Labeling; Gluten-Free Labeling of Fermented or Hydrolyzed Foods,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-18T05:00:00Z,2015,11,2015-11-18T05:00:00Z,2016-02-17T04:59:59Z,2016-02-17T22:00:37Z,2015-29292,0,0,0900006481d54997
FDA-2011-N-0103-0008,FDA,FDA-2011-N-0103,Microbiology Devices; Classification of In Vitro Diagnostic Devices for Bacillus Species Detection,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-17T05:00:00Z,2015,11,2015-11-17T05:00:00Z,2016-02-17T04:59:59Z,2015-12-10T22:00:47Z,2015-29275,0,0,0900006481d4d5ce
FDA-2014-N-1207-0001,FDA,FDA-2014-N-1207,"Use of the Term ‘‘Natural’’ in the Labeling of Human Food Products;
Request for Information and Comments",Proposed Rule,Request for Comment,2015-11-12T05:00:00Z,2015,11,2015-11-12T05:00:00Z,2016-02-11T04:59:59Z,2016-02-11T22:01:41Z,2015-28779,0,0,0900006481d386da
FDA-1998-N-0567-0002,FDA,FDA-1998-N-0567,"Revisions to the Requirements Applicable to Blood, Blood Components, and Source Plasma; Companion Document to Direct Final Rule",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-05T05:00:00Z,2015,11,1999-08-19T04:00:00Z,1999-12-04T04:59:59Z,2024-08-21T14:50:45Z,99-21293,0,0,090000648059b82d
FDA-2000-N-1098-0001,FDA,FDA-2000-N-1098,Revision to Requirements for Licensed Anti-Human Globulin and Blood Grouping Reagents; Companion to Direct Final Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-05T05:00:00Z,2015,11,2000-12-12T05:00:00Z,2001-02-27T04:59:59Z,2025-06-13T00:37:03Z,00–31587,0,0,09000064804edc14
FDA-1995-N-0376-0001,FDA,FDA-1995-N-0376,Disqualification of a Clinical Investigator,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-11-04T05:00:00Z,2015,11,1996-02-16T05:00:00Z,1996-05-17T03:59:59Z,2024-07-11T15:11:12Z,96-3384,0,0,090000648059a370
FDA-2015-D-3719-0001,FDA,FDA-2015-D-3719,"Draft Guidances Relating to the Regulation of Human Cells, Tissues, or Cellular or Tissue-Based Products; Public Hearing; Request for Comments",Proposed Rule,Notice of Hearing,2015-10-30T04:00:00Z,2015,10,2015-10-30T04:00:00Z,2016-04-30T03:59:59Z,2024-11-12T05:48:23Z,2015-27703,1,0,0900006481cfca62
FDA-2015-D-3581-0001,FDA,FDA-2015-D-3581,"Homologous Use of Human Cells, Tissues, and Cellular and Tissue-Based Products; Draft Guidance for Industry and Food and Drug Administration Staff; Availability",Proposed Rule,GDL Guidance,2015-10-30T04:00:00Z,2015,10,2015-10-30T04:00:00Z,2016-04-30T03:59:59Z,2024-11-12T05:48:43Z,2015-27704,1,0,0900006481cfcaaa
FDA-2014-D-1856-0061,FDA,FDA-2014-D-1856,"Human Cells, Tissues, and Cellular and Tissue-Based Products From 
Adipose Tissue: Regulatory Considerations; Draft Guidance for Industry; 
Reopening of the Comment Period",Proposed Rule,Reopening of Comment Period,2015-10-30T04:00:00Z,2015,10,2015-10-30T04:00:00Z,2016-04-30T03:59:59Z,2024-11-07T23:24:13Z,2015-27706,1,0,0900006481cfc915
FDA-2014-D-1584-0194,FDA,FDA-2014-D-1584,Same Surgical Procedure Exception: Questions and Answers Regarding the Scope of the Exception; Draft Guidance for Industry; Reopening of the Comment Period,Proposed Rule,Reopening of Comment Period,2015-10-30T04:00:00Z,2015,10,2015-10-30T04:00:00Z,2016-04-30T03:59:59Z,2024-11-12T05:48:23Z,2015-27707,1,0,0900006481cfca14
FDA-2014-D-1696-0052,FDA,FDA-2014-D-1696,"Minimal Manipulation of Human Cells, Tissues, and Cellular and Tissue-Based Products; Draft Guidance for Industry and Food and Drug Administration Staff; Reopening of the Comment Period",Proposed Rule,Reopening of Comment Period,2015-10-30T04:00:00Z,2015,10,2015-10-30T04:00:00Z,2016-04-30T03:59:59Z,2024-11-12T05:48:38Z,2015-27705,1,0,0900006481cfca64
FDA-2015-F-3663-0001,FDA,FDA-2015-F-3663,Grocery Manufacturers Association; Filing of Food Additive Petition,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-10-28T04:00:00Z,2015,10,2015-10-28T04:00:00Z,2015-11-28T04:59:59Z,2015-12-24T22:00:45Z,2015-27277,0,0,0900006481cf5410
FDA-2012-N-1210-0705,FDA,FDA-2012-N-1210,Food Labeling: Revision of the Nutrition and Supplement Facts Labels; Reopening of the Comment Period,Proposed Rule,Extension of Comment Period,2015-10-20T04:00:00Z,2015,10,2015-10-20T04:00:00Z,2015-10-24T03:59:59Z,2015-10-28T01:30:43Z,2015-26636,0,0,0900006481cd89e2
FDA-2015-N-0701-0001,FDA,FDA-2015-N-0701,"General Hospital and Personal Use Devices: Renaming of Pediatric
Hospital Bed Classification and Designation of Special Controls for
Pediatric Medical Crib; Classification of Medical Bassinet",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-10-08T04:00:00Z,2015,10,2015-10-08T04:00:00Z,2015-12-08T04:59:59Z,2015-12-08T22:00:30Z,2015-25627,0,0,0900006481cb9fbd
FDA-2015-N-2002-0001,FDA,FDA-2015-N-2002,"Clarification of When Products Made or Derived From Tobacco Are 
Regulated as Drugs, Devices, or Combination Products; Amendments to 
Regulations Regarding ``Intended Uses''",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-09-25T04:00:00Z,2015,9,2015-09-25T04:00:00Z,2015-11-25T04:59:59Z,2016-01-15T22:00:58Z,2015-24313,0,0,0900006481c95e75
FDA-2015-N-2819-0001,FDA,FDA-2015-N-2819,Emergency Permit Control Regulations; Technical Amendment,Proposed Rule,Amendment,2015-09-22T04:00:00Z,2015,9,2015-09-22T04:00:00Z,2015-12-08T04:59:59Z,2015-11-14T02:31:29Z,2015-23614,0,0,0900006481c8b1f4
FDA-2015-N-0001-0085,FDA,FDA-2015-N-0001,"The Food and Drug Administration Food Safety Modernization Act: Final
Rules To Establish Requirements for Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human and Animal Food; Public Meeting",Proposed Rule,Public Meeting,2015-09-22T04:00:00Z,2015,9,2015-09-22T04:00:00Z,,2015-09-22T13:49:31Z,2015-24027,0,0,0900006481c8b931
FDA-2011-N-0146-0190,FDA,FDA-2011-N-0146,"User Fee Program To Provide for Accreditation of Third-Party Auditors/
Certification Bodies To Conduct Food Safety Audits and To Issue
Certifications; Correction",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-09-17T04:00:00Z,2015,9,2015-09-17T04:00:00Z,,2015-09-17T14:18:51Z,2015-23333,0,0,0900006481c7bc0f
FDA-2011-F-0172-0573,FDA,FDA-2011-F-0172,"A Labeling Guide for Restaurants and Retail Establishments Selling Away-
From-Home Foods—Part II (Menu Labeling Requirements in Accordance
with the Patient Protection Affordable Care Act of 2010); Draft Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2015-09-16T04:00:00Z,2015,9,2015-09-16T04:00:00Z,2015-11-03T04:59:59Z,2015-11-04T02:30:26Z,2015-23232,0,0,0900006481c72826
FDA-2012-N-1210-0598,FDA,FDA-2012-N-1210,"Food Labeling: Revision of the Nutrition and Supplement Facts
Labels; Administrative Docket Update; Availability",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-09-10T04:00:00Z,2015,9,2015-09-10T04:00:00Z,2015-10-14T03:59:59Z,2015-11-18T02:30:28Z,2015-22757,0,0,0900006481c65793
FDA-2015-N-0540-7641,FDA,FDA-2015-N-0540,"Homeopathic Product Regulation: Evaluating the Food and Drug
Administration’s Regulatory Framework After a Quarter-Century;
Reopening of the Comment Period",Proposed Rule,Reopening of Comment Period,2015-09-09T04:00:00Z,2015,9,2015-09-09T04:00:00Z,2015-11-10T04:59:59Z,2015-11-19T02:30:30Z,2015-22682,0,0,0900006481c61c16
FDA-2015-N-0648-0001,FDA,FDA-2015-N-0648,Designation of Official Names and Proper Names for Certain Biological Products,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-08-28T04:00:00Z,2015,8,2015-08-28T04:00:00Z,2015-11-13T04:59:59Z,2015-11-23T22:00:56Z,2015-21382,0,0,0900006481c41306
FDA-2015-N-1514-0090,FDA,FDA-2015-N-1514,"Nicotine Exposure Warnings and Child-Resistant Packaging for Liquid
Nicotine, Nicotine-Containing ELiquid (s), and Other Tobacco
Products; Request for Comments; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2015-08-24T04:00:00Z,2015,8,2015-08-24T04:00:00Z,2015-10-01T03:59:59Z,2015-10-21T01:30:31Z,2015-20759,0,0,0900006481c3442b
FDA-2015-F-2712-0001,FDA,FDA-2015-F-2712,Adisseo France S.A.S.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Amendment,2015-08-13T04:00:00Z,2015,8,2015-08-13T04:00:00Z,2015-09-15T03:59:59Z,2015-08-13T14:18:09Z,2015-19884,0,0,0900006481c1ce2d
FDA-2015-D-1839-0001,FDA,FDA-2015-D-1839,The Food and Drug Administration’s Policy on Declaring Small Amounts of Nutrients and Dietary Ingredients on Nutrition Labels; Draft Guidance for Industry; Availability,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-07-30T04:00:00Z,2015,7,2015-07-30T04:00:00Z,2015-09-29T03:59:59Z,2015-09-29T01:31:00Z,2015-18655,0,0,0900006481bb0c28
FDA-2012-N-1210-0537,FDA,FDA-2012-N-1210,Food Labeling: Nutrition and Supplement Facts Labels; Revision,Proposed Rule,Supplemental Notice of Proposed Rulemaking (SNPRM),2015-07-27T04:00:00Z,2015,7,2015-07-27T04:00:00Z,2015-10-14T03:59:59Z,2016-03-10T14:00:39Z,2015-17928,0,0,0900006481ba67b9
FDA-2012-N-1210-0536,FDA,FDA-2012-N-1210,"Food Labeling: Revision of the Nutrition and Supplement Facts
Labels; Reopening of the Comment Period as to Specific Documents",Proposed Rule,Reopening of Comment Period,2015-07-27T04:00:00Z,2015,7,2015-07-27T04:00:00Z,2015-09-26T03:59:59Z,2015-10-16T01:30:24Z,2015-17929,0,0,0900006481ba66e1
FDA-2011-N-0146-0181,FDA,FDA-2011-N-0146,User Fee Program To Provide for Accreditation of Third-Party Auditors/Certification Bodies To Conduct Food Safety Audits and To Issue Certifications,Proposed Rule,Amendment,2015-07-24T04:00:00Z,2015,7,2015-07-24T04:00:00Z,2015-10-08T03:59:59Z,2015-10-21T01:31:23Z,2015-18141,0,0,0900006481b9db5b
FDA-2015-F-2337-0001,FDA,FDA-2015-F-2337,Petitions for Rulemaking: Alzchem AG; Food Additive for Animal Use,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-07-16T04:00:00Z,2015,7,2015-07-16T04:00:00Z,2015-08-18T03:59:59Z,2015-07-29T01:30:43Z,2015-17379,0,0,0900006481b8ac87
FDA-1995-N-0127-0001,FDA,FDA-1995-N-0127,Protection of Human Subjects; Informed Consent; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-07-09T04:00:00Z,2015,7,1995-12-22T05:00:00Z,1996-03-22T04:59:59Z,2025-06-02T22:00:18Z,,0,0,090000648056e51e
FDA-2015-N-2103-0001,FDA,FDA-2015-N-2103,"Removal of Review and Reclassification Procedures for Biological Products Licensed Prior to July 1, 1972",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-07-02T04:00:00Z,2015,7,2015-07-02T04:00:00Z,2015-10-01T03:59:59Z,2015-07-17T11:47:46Z,2015-16367,0,0,0900006481b6728a
FDA-2015-N-1514-0001,FDA,FDA-2015-N-1514,"Nicotine Exposure Warnings and Child-Resistant Packaging for Liquid
Nicotine, Nicotine-Containing ELiquid(s), and Other Tobacco Products; Request for Comments",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-07-01T04:00:00Z,2015,7,2015-07-01T04:00:00Z,2015-09-01T03:59:59Z,2015-09-02T01:30:31Z,2015-16151,0,0,0900006481b63040
FDA-2015-N-1355-0001,FDA,FDA-2015-N-1355,"Use of Ozone-Depleting Substances; Request for Comment Concerning
Essential-Use Designations",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-06-29T04:00:00Z,2015,6,2015-06-29T04:00:00Z,2015-08-29T03:59:59Z,2015-08-22T01:30:54Z,2015-15902,0,0,0900006481b5acc4
FDA-2015-N-0540-2724,FDA,FDA-2015-N-0540,"Homeopathic Product Regulation: Evaluating the Food and Drug
Administration’s Regulatory Framework After a Quarter-Century;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2015-06-10T04:00:00Z,2015,6,2015-06-10T04:00:00Z,2015-08-22T03:59:59Z,2015-08-26T01:30:21Z,2015-14143,0,0,0900006481b291fb
FDA-2010-N-0155-0208,FDA,FDA-2010-N-0155,"Veterinary Feed Directive Regulation Questions and Answers; Draft
Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2015-06-03T04:00:00Z,2015,6,2015-06-03T04:00:00Z,2015-08-04T03:59:59Z,2015-08-01T01:30:46Z,2015-13394,0,0,0900006481b17b73
FDA-2012-N-0447-0066,FDA,FDA-2012-N-0447,Antimicrobial Animal Drug Sales and Distribution Reporting,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-05-20T04:00:00Z,2015,5,2015-05-20T04:00:00Z,2015-08-19T03:59:59Z,2015-09-02T01:30:28Z,2015-12081,0,0,0900006481aeb0af
FDA-2015-N-0101-0001,FDA,FDA-2015-N-0101,"Safety and Effectiveness of Health Care Antiseptics; Topical Antimicrobial
Drug Products for Over-the-Counter Human Use; Proposed Amendment of the Tentative Final Monograph; Reopening of Administrative Record",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-05-01T04:00:00Z,2015,5,2015-05-01T04:00:00Z,2015-10-29T03:59:59Z,2026-03-01T10:00:09Z,2015-10174,1,0,0900006481ac7268
FDA-2011-N-0830-0008,FDA,FDA-2011-N-0830,"Abbreviated New Drug Applications and 505(b)(2) Applications; Extension
of Comment Period",Proposed Rule,Extension of Comment Period,2015-04-24T04:00:00Z,2015,4,2015-04-24T04:00:00Z,2015-06-09T03:59:59Z,2015-06-10T01:30:47Z,2015-09523,0,0,0900006481ab8547
FDA-2015-C-1154-0001,FDA,FDA-2015-C-1154,E. & J. Gallo Winery; Filing of Color Additive Petition,Proposed Rule,Petition,2015-04-22T04:00:00Z,2015,4,2015-04-22T04:00:00Z,,2015-04-22T15:33:04Z,2015-09248,0,0,0900006481ab359f
FDA-1990-N-0172-0260,FDA,FDA-1990-N-0172,Food Labeling; Reference Daily Intakes and Daily Reference Values; Mandatory Status of Nutrition Labeling and Nutrient Content Revision; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-04-13T04:00:00Z,2015,4,2015-04-13T04:00:00Z,1992-02-26T04:59:59Z,2015-04-13T16:18:42Z,,0,0,090000648052dfcc
FDA-2015-N-0828-0002,FDA,FDA-2015-N-0828,"Performance Standards for Ionizing Radiation Emitting Products;
Fluoroscopic Equipment; Correction",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-04-13T04:00:00Z,2015,4,2015-04-13T04:00:00Z,2015-06-30T03:59:59Z,2015-04-13T14:31:37Z,2015-08361,0,0,0900006481aa14e1
FDA-2002-N-0323-0168,FDA,FDA-2002-N-0323,Amendments to Registration of Food Facilities,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-04-09T04:00:00Z,2015,4,2015-04-09T04:00:00Z,2015-06-09T03:59:59Z,2015-07-02T01:30:26Z,2015-08018,0,0,0900006481a96ddc
FDA-1990-N-0172-0249,FDA,FDA-1990-N-0172,"Food Labeling; Health Messages and Label Statements; Definitions of the Terms Cholesterol Free, Low Cholesterol, and Reduced Cholesterol; Reference Daily Intakes and Daily reference Values; Mandatory Status of Nutrition Labeling and Nutrient Content Revision; Serving Sizes",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-04-08T04:00:00Z,2015,4,,,2015-04-22T02:01:26Z,,0,0,090000648052df92
FDA-2000-N-0611-0001,FDA,FDA-2000-N-0611,Premarket Notice Concerning Bioengineered Foods,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-03-31T04:00:00Z,2015,3,2015-03-31T04:00:00Z,2001-04-04T03:59:59Z,2015-04-01T02:01:22Z,,0,0,09000064804ddd49
FDA-2015-N-0540-0001,FDA,FDA-2015-N-0540,"Homeopathic Product Regulation: Evaluating the Food and Drug
Administration’s Regulatory Framework After a Quarter-Century;
Public Hearing",Proposed Rule,Public Hearing,2015-03-27T04:00:00Z,2015,3,2015-03-27T04:00:00Z,2015-06-23T03:59:59Z,2015-06-27T01:31:16Z,2015-07018,0,0,0900006481a6c325
FDA-2001-N-0178-0009,FDA,FDA-2001-N-0178,Electronic Products; Performance Standard for Diagnostic X-Ray Systems and Their Major Components; Correction,Proposed Rule,Correction,2015-03-17T04:00:00Z,2015,3,,,2016-02-01T17:10:32Z,,0,0,09000064804e1595
FDA-2015-F-0714-0001,FDA,FDA-2015-F-0714,Natural Resources Defense Council et al.; Filing of Food Additive Petition,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-03-16T04:00:00Z,2015,3,2015-03-16T04:00:00Z,,2015-11-05T02:31:03Z,2015-05938,0,0,0900006481a4635f
FDA-2015-F-0537-0001,FDA,FDA-2015-F-0537,Natural Resources Defense Council et al.; Filing of Food Additive Petition,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-03-16T04:00:00Z,2015,3,2015-03-16T04:00:00Z,2015-05-16T03:59:59Z,2015-09-03T01:30:16Z,2015-05937,0,0,0900006481a461c4
FDA-2011-N-0830-0005,FDA,FDA-2011-N-0830,Abbreviated New Drug Applications and 505(b)(2) Applications,Proposed Rule,Correction,2015-03-13T04:00:00Z,2015,3,2015-03-13T04:00:00Z,,2015-03-13T16:28:12Z,C1-2015-01666,0,0,0900006481a4296e
FDA-2007-N-0363-0059,FDA,FDA-2007-N-0363,"Electronic Distribution of Prescribing Information for Human Prescription
Drugs, Including Biological Products; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2015-03-09T04:00:00Z,2015,3,2015-03-09T04:00:00Z,2015-05-19T03:59:59Z,2015-06-02T01:30:45Z,2015-05336,0,0,0900006481a342ea
FDA-2014-N-1168-0030,FDA,FDA-2014-N-1168,"Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives;
Public Hearing; Request for Comments",Proposed Rule,Request for Comment,2015-03-05T05:00:00Z,2015,3,2015-03-05T05:00:00Z,2015-06-27T03:59:59Z,2015-07-15T01:31:03Z,2015-05018,0,0,0900006481a2e176
FDA-1996-N-0006-0100,FDA,FDA-1996-N-0006,"Over-the-Counter Sunscreen Drug Products—Regulatory Status of
Enzacamene",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-25T05:00:00Z,2015,2,2015-02-25T05:00:00Z,2015-04-14T03:59:59Z,2015-02-25T17:40:37Z,2015-03884,0,0,0900006481a16b78
FDA-1978-N-0018-0775,FDA,FDA-1978-N-0018,"Over-the-Counter Sunscreen Drug Products—Regulatory Status of
Enzacamene",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-25T05:00:00Z,2015,2,2015-02-25T05:00:00Z,2015-04-14T03:59:59Z,2015-04-14T02:11:05Z,2015-03884,0,0,0900006481a1641f
FDA-2003-N-0196-0060,FDA,FDA-2003-N-0196,"Over-the-Counter Sunscreen Drug Products—Regulatory Status of
Enzacamene",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-25T05:00:00Z,2015,2,2015-02-25T05:00:00Z,2015-04-14T03:59:59Z,2015-03-23T02:01:20Z,2015-03884,0,0,0900006481a16b76
FDA-2008-N-0474-0018,FDA,FDA-2008-N-0474,"Over-the-Counter Sunscreen Drug Products—Regulatory Status of
Ecamsule",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-25T05:00:00Z,2015,2,2015-02-25T05:00:00Z,2015-04-14T03:59:59Z,2015-05-02T02:02:23Z,2015-03883,0,0,0900006481a16312
FDA-1992-N-0190-0032,FDA,FDA-1992-N-0190,Notice of Proposed Rule Reopening of Comment Period from FDA/CFSAN,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-24T05:00:00Z,2015,2,2015-02-24T05:00:00Z,1998-07-07T03:59:59Z,2015-02-24T19:24:17Z,,0,0,090000648052f63a
FDA-1992-N-0190-0009,FDA,FDA-1992-N-0190,Notice of Proposed Rule from FDA/CFSAN,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-23T05:00:00Z,2015,2,2015-02-23T05:00:00Z,1996-06-04T03:59:59Z,2015-02-23T21:39:51Z,,0,0,090000648052f61f
FDA-1992-N-0190-0001,FDA,FDA-1992-N-0190,"Labeling Declaration for F, D & C Yellow No. 6 and F, D & C Yellow No.5; Amendment of Standard of Identity for Cheese Product",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-23T05:00:00Z,2015,2,2015-02-23T05:00:00Z,1995-10-05T03:59:59Z,2015-02-23T20:53:20Z,,0,0,090000648052f616
FDA-2013-N-0500-0081,FDA,FDA-2013-N-0500,"Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products; Public Meeting; Request for Comments;
Reopening of the Comment Period",Proposed Rule,Public Meeting,2015-02-18T05:00:00Z,2015,2,2015-02-18T05:00:00Z,2015-04-28T03:59:59Z,2015-05-07T01:31:29Z,2015-03211,0,0,0900006481a078f5
FDA-2011-N-0830-0001,FDA,FDA-2011-N-0830,Abbreviated New Drug Applications and 505(b)(2) Applications,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-06T05:00:00Z,2015,2,2015-02-06T05:00:00Z,2015-05-08T03:59:59Z,2015-04-10T02:06:25Z,2015-01666,0,0,09000064819f78d2
FDA-2015-C-0245-0001,FDA,FDA-2015-C-0245,"Signature Brands, LLC; Filing of Color Additive Petition",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2015-02-05T05:00:00Z,2015,2,2015-02-05T05:00:00Z,,2015-02-05T15:16:50Z,2015-02239,0,0,09000064819f5483
FDA-2014-N-2244-0006,FDA,FDA-2014-N-2244,"Draft Environmental Impact Statement for the Proposed Rule, Standards for Growing, Harvesting, Packing, and Holding of Produce for Human
Consumption; Notice for Public Meeting on Draft Environmental Impact
Statement; Correction",Proposed Rule,Correction,2015-01-14T05:00:00Z,2015,1,2015-01-14T05:00:00Z,,2015-01-14T15:22:28Z,C1-2015-00205,0,0,09000064819c883d
FDA-2014-N-2244-0007,FDA,FDA-2014-N-2244,"Draft Environmental Impact Statement for the Proposed Rule, Standards for Growing, Harvesting, Packing, and Holding of Produce for Human
Consumption; Notice for Public Meeting on Draft Environmental Impact
Statement",Proposed Rule,Public Meeting,2015-01-14T05:00:00Z,2015,1,2015-01-14T05:00:00Z,2015-03-14T03:59:59Z,2015-03-15T02:00:43Z,2015-00564,0,0,09000064819c87c0
FDA-2014-N-2244-0001,FDA,FDA-2014-N-2244,See FR Document(s) ID FDA-2014-N-2244-0006 and FDA-2014-N-2244-0007,Proposed Rule,,2015-01-12T00:00:00Z,2015,1,,,2015-01-14T19:00:38Z,,0,1,09000064819c1d12
FDA-2014-F-2307-0001,FDA,FDA-2014-F-2307,"Humic Products Trade Association; Filing of Food Additive Petition
(Animal Use)",Proposed Rule,Petition,2015-01-06T05:00:00Z,2015,1,2015-01-06T05:00:00Z,2015-02-06T04:59:59Z,2015-01-14T03:00:56Z,2014-30932,0,0,09000064819a648a