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withdrawn,object_id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-1979-N-0409-0001,FDA,FDA-1979-N-0409,Blood and Blood Components; Error and Accident Reports - Notice of Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-31T05:00:00Z,2013,12,2013-12-31T05:00:00Z,1980-11-07T04:59:59Z,2014-05-08T14:18:07Z,,0,0,090000648055636a
FDA-1979-N-0307-0001,FDA,FDA-1979-N-0307,Allergenic Products; Proposed Testing and Labeling Requirements; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,1980-07-02T03:59:59Z,2014-06-18T16:36:34Z,,0,0,090000648055517f
FDA-1979-N-0309-0001,FDA,FDA-1979-N-0309,Additional Standards for Human Blood Products; Antihemophillic Factor (Human) - Notice of Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,,2014-05-13T14:33:51Z,,0,0,090000648055519b
FDA-1979-N-0084-0001,FDA,FDA-1979-N-0084,Food Labeling; Net Weight Labeling Requirements - Notice of Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,1980-11-07T04:59:59Z,2014-05-12T18:31:25Z,,0,0,0900006480553e82
FDA-1980-N-0149-0001,FDA,FDA-1980-N-0149,Withdrawal of Certain Pre-1986 Proposed Rules - Notice of Proposed Rulemaking,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,,2014-05-08T12:45:51Z,,0,0,09000064805bcf5d
FDA-2013-N-0500-0006,FDA,FDA-2013-N-0500,Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products; Correction and Extension of Comment Period,Proposed Rule,Extension of Comment Period,2013-12-27T05:00:00Z,2013,12,2013-12-27T05:00:00Z,2014-03-14T03:59:59Z,2014-04-10T01:02:03Z,2013-30881,0,0,09000064814debad
FDA-2013-N-1563-0001,FDA,FDA-2013-N-1563,"Appendix 4 to Draft Qualitative Risk Assessment of Risk of Activity/Food
Combinations for Activities (Outside the Farm Definition) Conducted in a
Facility Co-Located on a Farm; Availability",Proposed Rule,Request for Comment,2013-12-24T05:00:00Z,2013,12,2013-12-24T05:00:00Z,2014-04-01T03:59:59Z,2014-01-01T02:04:13Z,2013-30375,0,0,09000064814d536f
FDA-2013-N-1425-0001,FDA,FDA-2013-N-1425,"Focused Mitigation Strategies To Protect Food Against Intentional
Adulteration; Public Meeting on Proposed Rule",Proposed Rule,Public Meeting,2013-12-24T05:00:00Z,2013,12,2013-12-24T05:00:00Z,,2013-12-24T15:38:06Z,2013-30372,0,0,09000064814d54bf
FDA-2013-N-1425-0002,FDA,FDA-2013-N-1425,Focused Mitigation Strategies to Protect Food Against Intentional Adulteration,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-12-24T05:00:00Z,2013,12,2013-12-24T05:00:00Z,2014-04-01T03:59:59Z,2014-04-04T01:02:32Z,2013-30373,0,0,09000064814d53fc
FDA-2013-F-1540-0001,FDA,FDA-2013-F-1540,Food Additive Petitions; Animal Use: DSM Nutritional Products,Proposed Rule,Petition,2013-12-23T05:00:00Z,2013,12,2013-12-23T05:00:00Z,2014-01-23T04:59:59Z,2014-01-14T19:58:32Z,2013-30461,0,0,09000064814d2f4a
FDA-2013-F-1539-0001,FDA,FDA-2013-F-1539,DSM Nutritional Products; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2013-12-23T05:00:00Z,2013,12,2013-12-23T05:00:00Z,2014-01-23T04:59:59Z,2024-11-07T23:01:24Z,2013-30462,1,0,09000064814d308c
FDA-1975-N-0012-0317,FDA,FDA-1975-N-0012,"Safety and Effectiveness of Consumer 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),2013-12-17T05:00:00Z,2013,12,2013-12-17T05:00:00Z,2015-02-17T04:59:59Z,2018-02-16T22:20:40Z,2013-29814,0,0,09000064814c4d8a
FDA-2010-N-0155-0139,FDA,FDA-2010-N-0155,Veterinary Feed Directive,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2013-12-12T05:00:00Z,2013,12,2013-12-12T05:00:00Z,2014-03-13T03:59:59Z,2015-06-02T16:57:20Z,2013-29696,0,0,09000064814ba038
FDA-2013-N-1523-0001,FDA,FDA-2013-N-1523,"Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act; Request for Nominations",Proposed Rule,Request for Information,2013-12-04T05:00:00Z,2013,12,2013-12-04T05:00:00Z,2014-03-05T04:59:59Z,2014-03-11T01:02:11Z,2013-28980,0,0,09000064814a61e6
FDA-2013-N-1525-0001,FDA,FDA-2013-N-1525,"List of Bulk Drug Substances That May Be Used in Pharmacy Compounding; Bulk Drug Substances That May Be Used To Compound Drug Products in Accordance With Section 503A of the Federal Food, Drug, and Cosmetic Act",Proposed Rule,Withdrawal,2013-12-04T05:00:00Z,2013,12,2013-12-04T05:00:00Z,2014-03-05T04:59:59Z,2014-10-03T01:02:26Z,2013-28979,0,0,09000064814a631f
FDA-2013-N-1524-0001,FDA,FDA-2013-N-1524,"Bulk Drug Substances that May be Used to Compound Drug Products, etc., Concerning Outsourcing Facilities: Request for Nominations",Proposed Rule,Request for Information,2013-12-04T05:00:00Z,2013,12,2013-12-04T05:00:00Z,2014-03-05T04:59:59Z,2017-07-19T01:02:39Z,2013-28978,0,0,09000064814a6122
FDA-2013-N-0001-0109,FDA,FDA-2013-N-0001,Medical Gas Regulation Review Meeting; Correction,Proposed Rule,Public Meeting,2013-11-25T05:00:00Z,2013,11,2013-11-25T05:00:00Z,,2013-11-26T13:29:50Z,2013-28083,0,0,09000064814959de
FDA-2011-N-0143-0037,FDA,FDA-2011-N-0143,Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Extension of Comment Periods,Proposed Rule,Extension of Comment Period,2013-11-20T05:00:00Z,2013,11,2013-11-20T05:00:00Z,2014-01-28T04:59:59Z,2014-11-12T15:25:38Z,2013-27645,0,0,090000648148b9c5
FDA-2011-N-0146-0039,FDA,FDA-2011-N-0146,Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications; Extension of Comment Periods,Proposed Rule,Extension of Comment Period,2013-11-20T05:00:00Z,2013,11,2013-11-20T05:00:00Z,2014-01-28T04:59:59Z,2014-11-12T15:25:43Z,2013-27644,0,0,090000648148bc0e
FDA-2011-N-0920-0288,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Periods,Proposed Rule,Extension of Comment Period,2013-11-20T05:00:00Z,2013,11,2013-11-20T05:00:00Z,2013-11-23T04:59:59Z,2015-04-17T02:02:04Z,2013-27783,0,0,090000648148b9c3
FDA-2012-S-0782-0014,FDA,FDA-2012-S-0782,See  Docket ID FDA-2011-N-0921 for the Correct Federal Register Document for Comment Participation,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-11-20T05:00:00Z,2013,11,2013-11-20T05:00:00Z,2013-11-23T04:59:59Z,2015-10-19T20:06:56Z,2013-27784,0,0,090000648148bc43
FDA-2011-N-0921-0321,FDA,FDA-2011-N-0921,"Environmental Impact Statement for the Proposed Rule: Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2013-11-18T05:00:00Z,2013,11,2013-11-18T05:00:00Z,2014-03-16T03:59:59Z,2014-04-16T01:02:36Z,2013-27479,0,0,0900006481486c94
FDA-2013-N-0500-0001,FDA,FDA-2013-N-0500,Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-11-13T05:00:00Z,2013,11,2013-11-13T05:00:00Z,2014-01-14T04:59:59Z,2016-04-26T19:00:32Z,2013-26799,0,0,090000648147a982
FDA-2012-S-0782-0013,FDA,FDA-2012-S-0782,See  Docket ID FDA-2013-N-0501 for the Correct Federal Register Document for Comment Participation,Proposed Rule,Request for Comment,2013-11-13T05:00:00Z,2013,11,2013-11-13T05:00:00Z,2014-01-14T04:59:59Z,2024-11-12T05:24:30Z,,1,0,090000648147a7d5
FDA-2011-N-0898-0015,FDA,FDA-2011-N-0898,Permanent Discontinuance or Interruption in Manufacturing of Certain Drug or Biological Products,Proposed Rule,Request for Comment,2013-11-04T05:00:00Z,2013,11,2013-11-04T05:00:00Z,2014-01-04T04:59:59Z,2014-08-29T01:04:25Z,2013-25956,0,0,090000648146f1a4
FDA-2013-N-0001-0102,FDA,FDA-2013-N-0001,Medical Gas Regulation Review; Announcement of Public Meeting,Proposed Rule,Public Meeting,2013-11-01T04:00:00Z,2013,11,2013-11-01T04:00:00Z,,2013-11-01T15:09:59Z,2013-26056,0,0,090000648146bfde
FDA-2011-N-0922-0001,FDA,FDA-2011-N-0922,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals; Public Meeting on Proposed Rule,Proposed Rule,Public Meeting,2013-10-29T04:00:00Z,2013,10,2013-10-29T04:00:00Z,,2013-11-03T00:00:58Z,2013-25125,0,0,090000648146529f
FDA-2013-N-1043-0001,FDA,FDA-2013-N-1043,Draft Qualitative Risk Assessment of Risk of Activity/Animal Food Combinations for Activities (Outside the Farm Definition) Conducted in a Facility Co-Located on a Farm; Availability,Proposed Rule,Request for Comment,2013-10-29T04:00:00Z,2013,10,2013-10-29T04:00:00Z,2014-02-27T04:59:59Z,2024-11-12T05:22:42Z,2013-25124,1,0,0900006481464b4c
FDA-2011-N-0922-0002,FDA,FDA-2011-N-0922,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-10-29T04:00:00Z,2013,10,2013-11-01T04:00:00Z,2014-02-27T04:59:59Z,2015-01-28T13:39:04Z,2013-25126,0,0,0900006481466af9
FDA-2012-S-0782-0002,FDA,FDA-2012-S-0782,See  Docket ID FDA-2011-N-0922- for the Correct Federal Register Document for Comment Participation,Proposed Rule,,2013-10-29T00:00:00Z,2013,10,,,2022-04-21T14:11:13Z,,0,1,09000064814651d4
FDA-2012-N-0447-0028,FDA,FDA-2012-N-0447,Antimicrobial Animal Drug Sales and Distribution Annual Summary Report Data Tables,Proposed Rule,Request for Comment,2013-09-26T04:00:00Z,2013,9,2013-09-26T04:00:00Z,2013-11-26T04:59:59Z,2014-01-14T16:24:26Z,2013-23488,0,0,090000648143b90d
FDA-2011-N-0143-0028,FDA,FDA-2011-N-0143,Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meetings,Proposed Rule,Public Meeting,2013-09-18T04:00:00Z,2013,9,2013-09-18T04:00:00Z,,2014-02-05T14:07:48Z,2013-22655,0,0,0900006481429d03
FDA-2011-N-0146-0030,FDA,FDA-2011-N-0146,Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meetings,Proposed Rule,Public Meeting,2013-09-18T04:00:00Z,2013,9,2013-09-18T04:00:00Z,,2013-09-18T14:57:00Z,2013-22655,0,0,090000648142a07f
FDA-2013-C-1008-0001,FDA,FDA-2013-C-1008,Wm. Wrigley Jr. Company; Filing of Color Additive Petition,Proposed Rule,Petition,2013-09-17T04:00:00Z,2013,9,2013-09-17T04:00:00Z,,2013-09-17T15:14:29Z,2013-22522,0,0,090000648142765f
FDA-2013-N-0521-0079,FDA,FDA-2013-N-0521,"Menthol in Cigarettes, Tobacco Products; Request for Comments; Extension of Comment Period",Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2013-09-11T04:00:00Z,2013,9,2013-09-11T04:00:00Z,2013-11-23T04:59:59Z,2014-10-04T01:07:43Z,2013-22015,0,0,09000064813f31ff
FDA-2011-N-0921-0204,FDA,FDA-2011-N-0921,"Notice of Intent to Prepare an Environmental Impact Statement for the Proposed Rule, Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-08-19T04:00:00Z,2013,8,2013-08-19T04:00:00Z,2013-11-16T04:59:59Z,2014-05-25T00:06:34Z,2013-20087,0,0,09000064813b8a9c
FDA-2013-N-0888-0001,FDA,FDA-2013-N-0888,Dean Foods Company and WhiteWave Foods Company; Filing of Food Additive Petition,Proposed Rule,Petition,2013-08-16T04:00:00Z,2013,8,2013-08-16T04:00:00Z,,2013-08-16T13:33:11Z,2013-19915,0,0,09000064813b58ec
FDA-2011-N-0146-0027,FDA,FDA-2011-N-0146,Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meeting,Proposed Rule,Public Meeting,2013-08-16T04:00:00Z,2013,8,2013-08-16T04:00:00Z,,2013-09-04T18:04:49Z,2013-19961,0,0,09000064813b5836
FDA-2011-N-0143-0025,FDA,FDA-2011-N-0143,Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meeting,Proposed Rule,Public Meeting,2013-08-16T04:00:00Z,2013,8,2013-08-16T04:00:00Z,2014-01-28T04:59:59Z,2014-02-06T02:05:17Z,2013-19961,0,0,09000064813b5f99
FDA-1977-N-0421-0001,FDA,FDA-1977-N-0421,New Drugs for Investigational Use Availability of Draft of Bioresearch Monitoring Data Collection Form - Notice of Proposed Rulemaking,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-08-12T04:00:00Z,2013,8,2013-08-12T04:00:00Z,,2013-08-13T12:26:29Z,,0,0,09000064805ef588
FDA-1977-N-0162-0001,FDA,FDA-1977-N-0162,Drugs for Human and Veterinary Use Public Disclosure of Specifications - Notice of Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-08-12T04:00:00Z,2013,8,2013-08-12T04:00:00Z,1977-09-14T03:59:59Z,2013-08-13T01:01:41Z,,0,0,09000064805db106
FDA-2011-N-0921-0199,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Comment Periods",Proposed Rule,Extension of Comment Period,2013-08-09T04:00:00Z,2013,8,2013-08-09T04:00:00Z,2013-11-23T04:59:59Z,2015-04-15T02:01:08Z,2013-19302,0,0,09000064813a84a8
FDA-2011-N-0920-0188,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Periods,Proposed Rule,Extension of Comment Period,2013-08-09T04:00:00Z,2013,8,2013-08-09T04:00:00Z,2013-11-23T04:59:59Z,2014-11-21T03:02:32Z,2013-19300,0,0,09000064813a8674
FDA-2011-N-0146-0024,FDA,FDA-2011-N-0146,Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-07-29T04:00:00Z,2013,7,2013-07-29T04:00:00Z,2013-11-27T04:59:59Z,2014-09-13T01:06:47Z,2013-17994,0,0,09000064813823a9
FDA-2011-N-0143-0023,FDA,FDA-2011-N-0143,Foreign Supplier Verification Programs for Importers of Food for Humans and Animals,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-07-29T04:00:00Z,2013,7,2013-07-29T04:00:00Z,2013-11-27T04:59:59Z,2014-07-01T01:02:50Z,2013-17993,0,0,090000648138252e
FDA-2013-N-0639-0002,FDA,FDA-2013-N-0639,Turtles Intrastate and Interstate Requirements; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-07-25T04:00:00Z,2013,7,2013-07-25T04:00:00Z,2013-10-09T03:59:59Z,2013-07-31T01:02:34Z,2013-17752,0,0,090000648137c594
FDA-2012-S-0782-0010,FDA,FDA-2012-S-0782,"See FDA-2000-N-0190-0111 Check to see if all the comments were moved, too",Proposed Rule,GDL Guidance,2013-07-24T04:00:00Z,2013,7,2013-07-24T04:00:00Z,2013-09-24T03:59:59Z,2015-10-19T20:14:20Z,2013-17750,0,0,0900006481379e60
FDA-2013-N-0521-0001,FDA,FDA-2013-N-0521,"Menthol in Cigarettes, Tobacco Products; Request for Comments",Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2013-07-24T04:00:00Z,2013,7,2013-07-24T04:00:00Z,2013-09-24T03:59:59Z,2014-10-12T00:15:23Z,2013-17805,0,0,0900006481379dc2
FDA-2013-F-0700-0001,FDA,FDA-2013-F-0700,Richard C. Theuer; Filing of Food Additive Petition and Citizen Petition,Proposed Rule,Petition,2013-07-19T04:00:00Z,2013,7,2013-07-19T04:00:00Z,,2013-07-19T19:15:31Z,2013-17330,0,0,090000648137061b
FDA-1998-C-0381-0001,FDA,FDA-1998-C-0381,Sensient Technologies Corporation; Withdrawal of Color Additive Petition,Proposed Rule,Withdrawal,2013-07-19T04:00:00Z,2013,7,2013-07-19T04:00:00Z,,2013-07-19T18:59:13Z,2013-17382,0,0,0900006481370520
FDA-2013-N-0365-0003,FDA,FDA-2013-N-0365,Administrative Detention of Drugs Intended for Human or Animal Use,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-07-15T04:00:00Z,2013,7,2013-07-15T04:00:00Z,2013-09-14T03:59:59Z,2013-09-20T19:31:48Z,2013-16843,0,0,09000064813667d8
FDA-1990-N-0172-0001,FDA,FDA-1990-N-0172,Food Labeling; Reference Daily Intakes and Daily Reference Values - Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-07-11T04:00:00Z,2013,7,1990-07-19T04:00:00Z,1990-11-17T04:59:59Z,2015-04-25T21:55:33Z,,0,0,090000648052dbee
FDA-2013-N-0568-0002,FDA,FDA-2013-N-0568,Physical Medicine Devices; Reclassification of Stair-Climbing Wheelchairs; Correction,Proposed Rule,Correction,2013-07-02T04:00:00Z,2013,7,2013-07-02T04:00:00Z,2013-09-11T03:59:59Z,2014-01-14T13:49:53Z,2013-15789,0,0,09000064813515e5
FDA-2012-N-0303-0003,FDA,FDA-2012-N-0303,Gastroenterology-Urology Devices; Reclassification of Implanted Blood Access Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-28T04:00:00Z,2013,6,2013-06-28T04:00:00Z,2013-07-30T03:59:59Z,2014-01-14T13:32:34Z,2013-15504,0,0,0900006481348988
FDA-2011-N-0070-0001,FDA,FDA-2011-N-0070,Laser Products; Proposed Amendment to Performance Standard,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-24T04:00:00Z,2013,6,2013-06-24T04:00:00Z,2013-09-24T03:59:59Z,2014-01-14T13:55:12Z,2013-14846,0,0,090000648133b662
FDA-2013-N-0684-0001,FDA,FDA-2013-N-0684,"Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments",Proposed Rule,Public Meeting,2013-06-20T04:00:00Z,2013,6,2013-06-20T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:35:39Z,2013-14549,0,0,0900006481333a7d
FDA-2013-N-0685-0001,FDA,FDA-2013-N-0685,"Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments",Proposed Rule,Public Meeting,2013-06-20T04:00:00Z,2013,6,2013-06-20T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:37:38Z,2013-14549,0,0,0900006481333a7e
FDA-2013-N-0581-0001,FDA,FDA-2013-N-0581,"Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary Syndrome, Cardiac and Non-Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for IABP for Other Specific Intended Uses",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-19T04:00:00Z,2013,6,2013-06-19T04:00:00Z,2013-09-18T03:59:59Z,2014-01-14T13:53:46Z,2013-14553,0,0,0900006481331179
FDA-2013-N-0683-0001,FDA,FDA-2013-N-0683,"Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments",Proposed Rule,Public Meeting,2013-06-19T04:00:00Z,2013,6,2013-06-19T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:35:08Z,2013-14549,0,0,0900006481331053
FDA-2013-N-0544-0001,FDA,FDA-2013-N-0544,Microbiology Devices; Reclassification of Nucleic Acid-Based Systems for Mycobacterium tuberculosis Complex in Respiratory Specimens,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-19T04:00:00Z,2013,6,2013-06-19T04:00:00Z,2013-08-20T03:59:59Z,2014-01-14T13:41:49Z,2013-14552,0,0,09000064813310ab
FDA-2013-N-0568-0001,FDA,FDA-2013-N-0568,Physical Medicine Devices; Reclassification of Stair-Climbing Wheelchairs,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-12T04:00:00Z,2013,6,2013-06-12T04:00:00Z,2013-09-11T03:59:59Z,2014-01-14T13:49:44Z,2013-13864,0,0,090000648131aeee
FDA-2012-N-1037-0013,FDA,FDA-2012-N-1037,Establishing a List of Qualifying Pathogens Under the Food and Drug Administration Safety and Innovation Act,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-12T04:00:00Z,2013,6,2013-06-12T04:00:00Z,2013-08-13T03:59:59Z,2014-01-14T13:36:59Z,2013-13865,0,0,090000648131adbc
FDA-2012-N-0920-0001,FDA,FDA-2012-N-0920,"Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-05-31T04:00:00Z,2013,5,2013-05-31T04:00:00Z,2013-08-15T03:59:59Z,2014-07-10T13:46:56Z,2013-12927,0,0,0900006481304148
FDA-2013-N-0487-0001,FDA,FDA-2013-N-0487,Cardiovascular Devices; Reclassification of External Counter-Pulsating Devices for Treatment of Chronic Stable Angina; Effective Date of Requirement for Premarket Approval for External Counter-Pulsating Devices for Other Specified Intended Uses,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-05-21T04:00:00Z,2013,5,2013-05-21T04:00:00Z,2013-08-20T03:59:59Z,2014-01-14T13:41:03Z,2013-12122,0,0,09000064812efb10
FDA-2008-F-0462-0003,FDA,FDA-2008-F-0462,Zentox Corporation; Withdrawal of Food Additive Petition,Proposed Rule,Withdrawal,2013-05-14T04:00:00Z,2013,5,2013-05-14T04:00:00Z,,2013-05-14T14:06:42Z,2013-11499,0,0,09000064812e2e2e
FDA-2013-N-0461-0001,FDA,FDA-2013-N-0461,"General and Plastic Surgery Devices: Reclassification of Ultraviolet Lamps for Tanning, Henceforth To Be Known as Sunlamp Products",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-05-09T04:00:00Z,2013,5,2013-05-09T04:00:00Z,2013-08-08T03:59:59Z,2014-05-21T01:08:27Z,2013-10982,0,0,09000064812d1aaa
FDA-2013-N-0402-0001,FDA,FDA-2013-N-0402,Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives Public Meeting; Request for Comments,Proposed Rule,Public Meeting,2013-05-09T04:00:00Z,2013,5,2013-05-09T04:00:00Z,2013-06-08T03:59:59Z,2014-03-06T17:14:13Z,2013-11007,0,0,09000064812d1dcc
FDA-2012-S-0782-0007,FDA,FDA-2012-S-0782,See  Document ID FDA–2013-D-0446-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,GDL Guidance,2013-05-09T04:00:00Z,2013,5,2013-05-09T04:00:00Z,2013-07-09T03:59:59Z,2015-10-19T20:13:48Z,,0,0,09000064812d1aac
FDA-2012-S-0782-0008,FDA,FDA-2012-S-0782,See  Document ID FDA-2013-D-0447-0011 for the Correct Federal Register Document for Comment Participation,Proposed Rule,GDL Guidance,2013-05-09T04:00:00Z,2013,5,2013-05-09T04:00:00Z,2013-07-09T03:59:59Z,2015-10-19T20:13:59Z,2013-11006,0,0,09000064812d1be7
FDA-2011-N-0920-0017,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Periods,Proposed Rule,Extension of Comment Period,2013-04-26T04:00:00Z,2013,4,2013-04-26T04:00:00Z,2013-08-09T03:59:59Z,2013-08-12T01:02:35Z,2013-09763,0,0,09000064812a946e
FDA-2012-N-1258-0003,FDA,FDA-2012-N-1258,Draft Qualitative Risk Assessment of Risk of Activity/Food Combinations for Activities (Outside the Farm Definition) Conducted in Facility Co-Located on Farm; Availability: Extension of Comment Period,Proposed Rule,Extension of Comment Period,2013-04-26T04:00:00Z,2013,4,2013-04-26T04:00:00Z,2013-09-17T03:59:59Z,2013-09-17T01:02:45Z,2013-09762,0,0,09000064812a94a4
FDA-2011-N-0921-0087,FDA,FDA-2011-N-0921,"Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: Extension of comment periods",Proposed Rule,Extension of Comment Period,2013-04-26T04:00:00Z,2013,4,2013-04-26T04:00:00Z,2013-08-09T03:59:59Z,2013-10-01T01:01:59Z,2013-09761,0,0,09000064812a94a8
FDA-2013-N-0125-0001,FDA,FDA-2013-N-0125,Use of Certain Symbols in Labeling,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-04-19T04:00:00Z,2013,4,2013-04-19T04:00:00Z,2013-06-19T03:59:59Z,2013-06-25T01:28:35Z,2013-09175,0,0,090000648129c6c1
FDA-2013-N-0067-0001,FDA,FDA-2013-N-0067,Infant Formula: The Addition of Minimum and Maximum Levels of Selenium to Infant Formula and Related Labeling Requirements,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-04-16T04:00:00Z,2013,4,2013-04-16T04:00:00Z,2013-07-02T03:59:59Z,2013-07-02T01:02:24Z,2013-08855,0,0,0900006481295cad
FDA-2013-N-0365-0001,FDA,FDA-2013-N-0365,Administrative Detention under the Food and Drug Administration Safety and Innovation Act,Proposed Rule,Request for Comment,2013-04-09T04:00:00Z,2013,4,2013-04-09T04:00:00Z,2013-05-10T03:59:59Z,2013-09-20T19:30:59Z,2013-08120,0,0,0900006481289e68
FDA-2013-N-0195-0001,FDA,FDA-2013-N-0195,Effective Date of Requirement for Premarket Approval for Three Class III Preamendments Devices: Reclassification of Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-04-04T04:00:00Z,2013,4,2013-04-04T04:00:00Z,2013-05-07T03:59:59Z,2014-05-07T01:03:54Z,2013-07730,0,0,0900006481268b15
FDA-2012-S-0782-0006,FDA,FDA-2012-S-0782,See  Document ID FDA-2013-D-0269-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,GDL Guidance,2013-03-26T04:00:00Z,2013,3,2013-03-26T04:00:00Z,2013-05-29T03:59:59Z,2015-10-19T20:13:38Z,2013-06824,0,0,090000648124521d
FDA-2013-N-0234-0001,FDA,FDA-2013-N-0234,Effective Dates of Requirements for Premarket Approvals: Automated External Defibrillator System,Proposed Rule,,2013-03-25T04:00:00Z,2013,3,2013-03-25T04:00:00Z,2013-06-25T03:59:59Z,2013-07-02T01:02:15Z,2013-06723,0,0,09000064812417a6
FDA-2012-S-0782-0005,FDA,FDA-2012-S-0782,See  Document ID FDA-2013-N-0260-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,Request for Comment,2013-03-22T04:00:00Z,2013,3,2013-03-22T04:00:00Z,2013-05-22T03:59:59Z,2015-10-19T20:13:29Z,,0,0,090000648123d4b1
FDA-2011-N-0921-0056,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Correction",Proposed Rule,Correction,2013-03-20T04:00:00Z,2013,3,2013-03-20T04:00:00Z,,2013-03-20T20:13:12Z,2013-06357,0,0,0900006481237518
FDA-2011-N-0920-0015,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Correction,Proposed Rule,Correction,2013-03-20T04:00:00Z,2013,3,2013-03-20T04:00:00Z,,2013-03-21T05:06:31Z,2013-06356,0,0,090000648123737e
FDA-2012-S-0782-0004,FDA,FDA-2012-S-0782,See  Document ID FDA-2013-N-0227-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,,2013-03-19T00:00:00Z,2013,3,,,2022-04-21T14:11:13Z,,0,1,0900006481234c8f
FDA-2012-N-1258-0002,FDA,FDA-2012-N-1258,Draft Qualitative Risk Assessment of Risk of Activity/Food Combinations: Activities Outside the Farm Definition Conducted in a Facility Co-Located on a Farm; Availability; Reopening of the Comment Period,Proposed Rule,Reopening of Comment Period,2013-03-13T04:00:00Z,2013,3,2013-03-13T04:00:00Z,2013-05-17T03:59:59Z,2013-04-27T01:01:43Z,2013-05730,0,0,0900006481227969
FDA-2012-F-1100-0002,FDA,FDA-2012-F-1100,See FDA-2012-F-1100-0001,Proposed Rule,,2013-03-04T00:00:00Z,2013,3,,,2013-03-04T17:13:40Z,,0,1,0900006481216dbf
FDA-2013-N-0080-0001,FDA,FDA-2013-N-0080,Human Subject Protection: Acceptance of Data from Clinical Studies for Medical Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-02-25T05:00:00Z,2013,2,2013-02-25T05:00:00Z,2013-05-29T03:59:59Z,2014-01-14T13:16:22Z,2013-04201,0,0,0900006481206965
FDA-2009-P-0147-0012,FDA,FDA-2009-P-0147,Flavored Milk; Petition to Amend the Standard of Identity for Milk and 17 Additional Dairy Products,Proposed Rule,Request for Comment,2013-02-20T05:00:00Z,2013,2,2013-02-20T05:00:00Z,2013-05-22T03:59:59Z,2014-12-13T03:05:42Z,2013-03835,0,0,09000064811fe498
FDA-2011-N-0921-0028,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Notice of  Extension of Comment Period for Information Collection Provisions",Proposed Rule,Extension of Comment Period,2013-02-19T05:00:00Z,2013,2,2013-02-19T05:00:00Z,2013-11-23T04:59:59Z,2014-01-09T02:02:43Z,2013-03778,0,0,09000064811fd0b0
FDA-2011-N-0920-0013,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Period for Information Collection Provisions,Proposed Rule,Extension of Comment Period,2013-02-19T05:00:00Z,2013,2,2013-02-19T05:00:00Z,2013-11-16T04:59:59Z,2013-11-16T21:04:02Z,2013-03732,0,0,09000064811fcf74
FDA-2009-N-0458-0011,FDA,FDA-2009-N-0458,"Medical Devices; Pediatric Uses of Devices: Requirement for Submission of Information on Pediatric Subpopulations that Suffer from a Disease or Condition that a Device is Intended to Treat, Diagnose, or Cure",Proposed Rule,Supplemental Notice of Proposed Rulemaking (SNPRM),2013-02-19T05:00:00Z,2013,2,2013-02-19T05:00:00Z,2013-04-23T03:59:59Z,2014-01-13T19:10:40Z,2013-03647,0,0,09000064811fced6
FDA-2011-N-0921-0027,FDA,FDA-2011-N-0921,"Food and Drug Administration Food Safety Modernization Act: Proposed Rules To Establish Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption and for Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Notification of Public Meeting",Proposed Rule,Public Meeting,2013-02-13T05:00:00Z,2013,2,2013-02-13T05:00:00Z,,2013-04-15T14:29:44Z,2013-03316,0,0,09000064811f7534
FDA-2011-N-0920-0012,FDA,FDA-2011-N-0920,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption and for Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Public Meeting",Proposed Rule,Public Meeting,2013-02-13T05:00:00Z,2013,2,2013-02-13T05:00:00Z,,2013-02-13T15:02:12Z,2013-03316,0,0,09000064811f6fb1
FDA-2013-N-0069-0001,FDA,FDA-2013-N-0069,Medical Devices; Ophthalmic Devices: Classification of the Eyelid Weight,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-02-08T05:00:00Z,2013,2,2013-02-08T05:00:00Z,2013-05-10T03:59:59Z,2013-05-10T01:05:34Z,2013-02862,0,0,09000064811ee67b
FDA-2012-N-1239-0001,FDA,FDA-2012-N-1239,Dental Devices: Reclassification of Temporary Mandibular Condyle Prosthesis,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-02-07T05:00:00Z,2013,2,2013-02-07T05:00:00Z,2013-05-09T03:59:59Z,2014-01-14T13:06:51Z,2013-02688,0,0,09000064811ea30e
FDA-1981-N-0083-0033,FDA,FDA-1981-N-0083,FDA  - Sublifting Agents; Proposed Affirmation of GRAS Status with Specific Limitations; Removal from GRAS Status as Direct Human Food Ingredient; Reopening of Comment Period,Proposed Rule,Reopening of Comment Period,2013-02-06T05:00:00Z,2013,2,2013-02-06T05:00:00Z,1982-12-08T04:59:59Z,2013-02-06T20:48:49Z,,0,0,09000064805af5a4
FDA-2011-N-0920-0011,FDA,FDA-2011-N-0920,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Public Meeting",Proposed Rule,Public Meeting,2013-01-31T05:00:00Z,2013,1,2013-01-31T05:00:00Z,2013-05-17T03:59:59Z,2013-05-03T01:03:58Z,2013-02089,0,0,09000064811e0986
FDA-2011-N-0921-0013,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Notice of Public Meeting",Proposed Rule,Public Meeting,2013-01-31T05:00:00Z,2013,1,2013-01-31T05:00:00Z,2013-05-17T03:59:59Z,2013-04-30T01:02:24Z,2013-02089,0,0,09000064811e0bbe
FDA-2012-N-1238-0001,FDA,FDA-2012-N-1238,Medical Devices: Ophthalmic Devices; Classification of Scleral Plug,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-01-25T05:00:00Z,2013,1,2013-01-25T05:00:00Z,2013-04-26T03:59:59Z,2013-01-25T14:43:07Z,2013-01447,0,0,09000064811d79e5
FDA-2011-N-0661-0001,FDA,FDA-2011-N-0661,Effective Date of Requirement for Premarket Approval for Two Class III Preamendments Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-01-18T05:00:00Z,2013,1,2013-01-18T05:00:00Z,2013-04-19T03:59:59Z,2013-10-29T01:02:17Z,2013-01006,0,0,09000064811c736d
FDA-2011-N-0920-0001,FDA,FDA-2011-N-0920,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls For Human Food,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-01-16T05:00:00Z,2013,1,2013-01-16T05:00:00Z,2013-05-17T03:59:59Z,2013-11-16T02:02:21Z,2013-00125,0,0,09000064811b194e
FDA-2011-N-0921-0001,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing and Holding of Produce for Human Consumption",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-01-16T05:00:00Z,2013,1,2013-01-16T05:00:00Z,2013-05-17T03:59:59Z,2014-09-05T01:02:05Z,2013-00123,0,0,09000064811b4301