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withdrawn,object_id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-1484-0001,FDA,FDA-2014-N-1484,Revisions to Exceptions Applicable to Certain Human Cells Tissues and Cellular and Tissue-Based Products,Proposed Rule,Amendment,2014-12-31T05:00:00Z,2014,12,2014-12-31T05:00:00Z,2015-04-01T03:59:59Z,2015-04-01T02:01:23Z,2014-30528,0,0,090000648199bdf0
FDA-2014-D-1856-0001,FDA,FDA-2014-D-1856,"Human Cells, Tissues, and Cellular and Tissue-Based Products From Adipose Tissue: Regulatory Considerations; Draft Guidance for Industry; Availability",Proposed Rule,Request for Comment,2014-12-24T05:00:00Z,2014,12,2014-12-24T05:00:00Z,2015-02-24T04:59:59Z,2015-02-24T03:13:21Z,2014-30142,0,0,09000064819914d3
FDA-2007-N-0363-0040,FDA,FDA-2007-N-0363,Electronic Distribution of Prescribing Information for Human Prescription Drugs Including Biological Products,Proposed Rule,Amendment,2014-12-18T05:00:00Z,2014,12,2014-12-18T05:00:00Z,2015-03-19T03:59:59Z,2015-03-19T02:14:33Z,2014-29522,0,0,0900006481982461
FDA-2012-D-1002-0003,FDA,FDA-2012-D-1002,"Questions and Answers Regarding Food Facility Registration (Sixth
Edition); Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2014-11-19T05:00:00Z,2014,11,2014-11-19T05:00:00Z,,2014-11-19T17:46:19Z,2014-27290,0,0,0900006481937eea
FDA-1999-N-0194-0008,FDA,FDA-1999-N-0194,"Additions and Modifications to the List of Drug Products That Have Been
Withdrawn or Removed From the Market for Reasons of Safety or
Effectiveness; Correction",Proposed Rule,Correction,2014-11-17T05:00:00Z,2014,11,2014-11-17T05:00:00Z,,2024-09-20T19:07:11Z,2014-27038,0,0,0900006481933127
FDA-2014-N-1205-0001,FDA,FDA-2014-N-1205,Orthopedic Devices: Reclassification of Thoracolumbosacral Rigid Pedicle Screw Systems; Classification and Effective Date of Requirement for Premarket Approval for Dynamic Stabilization Systems,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2014-11-12T05:00:00Z,2014,11,2014-11-12T05:00:00Z,2015-02-11T04:59:59Z,2015-02-12T03:01:00Z,2014-26726,0,0,0900006481926d14
FDA-2014-F-1669-0001,FDA,FDA-2014-F-1669,The Iams Company; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-11-06T05:00:00Z,2014,11,2014-11-06T05:00:00Z,2014-12-09T04:59:59Z,2014-11-16T02:07:52Z,2014-26405,0,0,090000648191b2b0
FDA-1975-N-0248-0003,FDA,FDA-1975-N-0248,Notice of Proposed Rulemaking re Polychlorinated Biphenyls (PCB's),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-11-06T05:00:00Z,2014,11,2014-11-06T05:00:00Z,1972-05-19T03:59:59Z,2017-11-11T21:32:14Z,,0,0,09000064805c6826
FDA-2011-N-0143-0259,FDA,FDA-2011-N-0143,Food and Drug Administration Food Safety Modernization Act: Meetings on Rule Revisions,Proposed Rule,Public Meeting,2014-10-23T04:00:00Z,2014,10,2014-10-23T04:00:00Z,,2014-10-23T17:19:43Z,2014-25261,0,0,09000064818f824b
FDA-2011-N-0920-1585,FDA,FDA-2011-N-0920,Food and Drug Administration Food Safety Modernization Act: Meetings on Rule Revisions,Proposed Rule,Public Meeting,2014-10-23T04:00:00Z,2014,10,2014-10-23T04:00:00Z,,2014-10-23T16:21:59Z,2014-25261,0,0,09000064818f6c1c
FDA-2011-N-0922-0356,FDA,FDA-2011-N-0922,Food and Drug Administration Food Safety Modernization Act: Meetings on Rule Revisions,Proposed Rule,Public Meeting,2014-10-23T04:00:00Z,2014,10,2014-10-23T04:00:00Z,,2014-10-23T17:18:06Z,2014-25261,0,0,09000064818f824a
FDA-2014-D-1584-0001,FDA,FDA-2014-D-1584,Same Surgical Procedure Exception Questions and Answers Regarding the Scope of the Exception; Draft Guidance for Industry; Availability,Proposed Rule,Request for Comment,2014-10-23T04:00:00Z,2014,10,2014-10-23T04:00:00Z,2014-12-23T04:59:59Z,2014-12-24T03:02:41Z,2014-25217,0,0,09000064818f6c17
FDA-2011-N-0921-1100,FDA,FDA-2011-N-0921,Food and Drug Administration Food Safety Modernization Act: Meetings on Rule Revisions,Proposed Rule,Public Meeting,2014-10-23T04:00:00Z,2014,10,2014-10-23T04:00:00Z,,2014-10-23T17:15:16Z,2014-25261,0,0,09000064818f8249
FDA-2014-C-1552-0001,FDA,FDA-2014-C-1552,"Colorcon, Inc.; Filing of Color Additive Petition",Proposed Rule,Petition,2014-10-22T04:00:00Z,2014,10,2014-10-22T04:00:00Z,,2014-10-22T17:46:35Z,2014-25089,0,0,09000064818e8230
FDA-2014-C-1616-0001,FDA,FDA-2014-C-1616,EMD Millipore Corp.; Filing of Color Additive Petition,Proposed Rule,Petition,2014-10-21T04:00:00Z,2014,10,2014-10-21T04:00:00Z,,2014-10-21T14:04:07Z,2014-24962,0,0,09000064818e403a
FDA-2014-F-1509-0001,FDA,FDA-2014-F-1509,DSM Nutritional Products; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-10-16T04:00:00Z,2014,10,2014-10-16T04:00:00Z,2014-11-18T04:59:59Z,2014-10-16T15:50:43Z,2014-24593,0,0,09000064818c7f40
FDA-2014-F-1370-0001,FDA,FDA-2014-F-1370,Casa de Mesquite LLC; Filing of Food Additive Petition,Proposed Rule,Petition,2014-10-03T04:00:00Z,2014,10,2014-10-03T04:00:00Z,,2014-10-03T20:21:13Z,2014-23597,0,0,09000064818a666c
FDA-1991-N-0365-0001,FDA,FDA-1991-N-0365,Legal Status of Approved labelings for Prescription Drugs; Prescribing for Uses Unapproved by the Food and Drug Administration; Notice of Proposed Rule Making,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-10-02T04:00:00Z,2014,10,2014-10-02T04:00:00Z,1972-10-16T03:59:59Z,2015-02-10T03:09:27Z,,0,0,0900006480530c39
FDA-2011-N-0143-0247,FDA,FDA-2011-N-0143,Foreign Supplier Verification Programs for Importers of Food for Humans and Animals,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-29T04:00:00Z,2014,9,2014-09-29T04:00:00Z,2014-12-16T04:59:59Z,2014-12-18T03:04:36Z,2014-22448,0,0,0900006481898ff6
FDA-2011-N-0922-0269,FDA,FDA-2011-N-0922,Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals,Proposed Rule,Supplemental Notice of Proposed Rulemaking (SNPRM),2014-09-29T04:00:00Z,2014,9,2014-09-29T04:00:00Z,2014-12-16T04:59:59Z,2015-01-07T03:01:27Z,2014-22445,0,0,0900006481898a7d
FDA-2011-N-0920-1553,FDA,FDA-2011-N-0920,"Current Good Manufacturing Practice and Hazard Analysis and Risk-Based
Preventive Controls for Human Food",Proposed Rule,Supplemental Notice of Proposed Rulemaking (SNPRM),2014-09-29T04:00:00Z,2014,9,2014-09-29T04:00:00Z,2014-12-16T04:59:59Z,2015-10-07T15:36:24Z,2014-22446,0,0,0900006481898a79
FDA-2011-N-0921-0973,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for
Human Consumption",Proposed Rule,Supplemental Notice of Proposed Rulemaking (SNPRM),2014-09-29T04:00:00Z,2014,9,2014-09-29T04:00:00Z,2014-12-16T04:59:59Z,2015-01-16T03:02:27Z,2014-22447,0,0,0900006481898f57
FDA-1978-N-0708-0002,FDA,FDA-1978-N-0708,Requirement for Estrogens; Labeling Directed to the Patient,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-24T04:00:00Z,2014,9,2014-09-24T04:00:00Z,1979-06-19T03:59:59Z,2014-09-24T13:32:05Z,44FR22752,0,0,090000648057cb3e
FDA-1991-N-0367-0001,FDA,FDA-1991-N-0367,Kanamycin Sulfate; Kanamycin B Content Testing Method,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-23T04:00:00Z,2014,9,2014-09-23T04:00:00Z,1969-05-27T03:59:59Z,2014-09-23T13:37:35Z,,0,0,0900006480531021
FDA-1978-N-0995-0002,FDA,FDA-1978-N-0995,Estrogens to Treat Postpartum Breast Engorgement; Proposed Requirements for Patient Labeling,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-23T04:00:00Z,2014,9,2014-09-23T04:00:00Z,1979-01-05T04:59:59Z,2014-09-23T14:25:56Z,,0,0,0900006480591673
FDA-2000-N-0158-0057,FDA,FDA-2000-N-0158,"Reclassification of Iontophoresis Devices Intended for Any Other
Purposes",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-22T04:00:00Z,2014,9,2014-09-22T04:00:00Z,2014-12-23T04:59:59Z,2014-12-23T03:01:11Z,2014-22453,0,0,0900006481885b66
FDA-1978-N-1796-0002,FDA,FDA-1978-N-1796,"Estradiol Benzoate, Progesterone, Testosterone Propionate, and Estadiol Monopalmitate for Use in Food-Producing Animals; Proposed Revocation of Provisions",Proposed Rule,Notice of Hearing,2014-09-22T04:00:00Z,2014,9,2014-09-22T04:00:00Z,1979-02-06T04:59:59Z,2014-09-22T18:58:37Z,,0,0,090000648059db3d
FDA-2014-N-1243-0001,FDA,FDA-2014-N-1243,"Dental Devices; Reclassification of Salivary Stimulatory System, To Be
Renamed Electrical Salivary Stimulator System",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-18T04:00:00Z,2014,9,2014-09-18T04:00:00Z,2014-12-18T04:59:59Z,2014-12-18T03:04:34Z,2014-22255,0,0,090000648187b694
FDA-1978-N-1254-0001,FDA,FDA-1978-N-1254,Bioresearch Monitoring Program,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-15T04:00:00Z,2014,9,2014-09-15T04:00:00Z,,2014-09-15T16:33:33Z,,0,0,09000064805994b4
FDA-2011-N-0650-0006,FDA,FDA-2011-N-0650,"Cardiovascular Devices; Reclassification of External Pacemaker
Pulse Generator Devices; Reclassification of Pacing System Analyzers",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-15T04:00:00Z,2014,9,2014-09-15T04:00:00Z,2014-12-16T04:59:59Z,2014-12-16T03:01:20Z,2014-21814,0,0,0900006481871aee
FDA-1985-N-0258-0001,FDA,FDA-1985-N-0258,Tests and Methods of Assay and Certification of Certain Antibiotic Drugs; Notice of Proposal to Delete Obsolete Sections,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-15T04:00:00Z,2014,9,2014-09-15T04:00:00Z,1965-12-07T04:59:59Z,2014-09-15T16:42:32Z,,0,0,09000064805b67ff
FDA-2011-N-0650-0005,FDA,FDA-2011-N-0650,Cardiovascular Devices; Withdrawal of Proposed Rule of Reclassification of External Pacemaker Pulse Generator Devices,Proposed Rule,Withdrawal,2014-09-15T04:00:00Z,2014,9,2014-09-15T04:00:00Z,,2014-09-15T14:39:00Z,2014-21816,0,0,0900006481871b7a
FDA-2014-N-1110-0004,FDA,FDA-2014-N-1110,"Revocation of General Safety Test Regulations That Are Duplicative of
Requirements in Biologics License Applications; Correction",Proposed Rule,Correction,2014-09-10T04:00:00Z,2014,9,2014-09-10T04:00:00Z,,2014-09-10T16:07:16Z,2014-21481,0,0,0900006481868371
FDA-1978-N-0997-0001,FDA,FDA-1978-N-0997,Hydrazine in Human Drug Products; Declaration of New Drug Status,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-09-05T04:00:00Z,2014,9,2014-09-05T04:00:00Z,1979-08-14T03:59:59Z,2014-09-05T14:36:29Z,44FR33694,0,0,09000064805917e6
FDA-2013-P-0472-0008,FDA,FDA-2013-P-0472,Richard C. Theuer; Withdrawal of Food Additive Petition and Citizen Petition,Proposed Rule,Withdrawal,2014-09-03T04:00:00Z,2014,9,2014-09-03T04:00:00Z,,2014-09-03T14:08:52Z,2014-20665,0,0,0900006481858a17
FDA-2013-F-0700-0002,FDA,FDA-2013-F-0700,Richard C. Theuer; Withdrawal of Food Additive Petition and Citizen Petition,Proposed Rule,Withdrawal,2014-09-02T04:00:00Z,2014,9,2014-09-02T04:00:00Z,,2014-09-03T13:55:03Z,2014-20665,0,0,0900006481853733
FDA-2014-N-1110-0001,FDA,FDA-2014-N-1110,"Revocation of General Safety Test Regulations That Are Duplicative of
Requirements in Biological License Applications",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-08-22T04:00:00Z,2014,8,2014-08-22T04:00:00Z,2014-11-21T04:59:59Z,2014-11-21T03:02:33Z,2014-19888,0,0,090000648183b252
FDA-2014-F-1184-0001,FDA,FDA-2014-F-1184,Zinpro Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-08-21T04:00:00Z,2014,8,2014-08-21T04:00:00Z,2014-09-23T03:59:59Z,2014-09-17T01:09:18Z,2014-19831,0,0,0900006481837f83
FDA-1978-C-0535-0001,FDA,FDA-1978-C-0535,Orange B Termination of Listing,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-08-19T04:00:00Z,2014,8,2014-08-19T04:00:00Z,1978-12-05T04:59:59Z,2014-08-19T13:33:41Z,43FR45611,0,0,090000648057369a
FDA-2014-N-1168-0001,FDA,FDA-2014-N-1168,"Generic Drug User Fee Amendments of 2012; Public Hearing on Policy
Development; Request for Comments",Proposed Rule,Notice of Hearing,2014-08-19T04:00:00Z,2014,8,2014-08-19T04:00:00Z,2014-10-14T03:59:59Z,2014-11-21T03:02:42Z,2014-19632,0,0,090000648182f82d
FDA-1978-N-2051-0002,FDA,FDA-1978-N-2051,"Estrogenic, Oral Contraceptive, and Progestational Drug Products; Proposed Requirements for Patient Labeling; Proposed Rule",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-08-18T04:00:00Z,2014,8,2014-08-18T04:00:00Z,1978-12-13T04:59:59Z,2014-08-18T16:14:11Z,,0,0,09000064805a205c
FDA-1978-N-0344-0001,FDA,FDA-1978-N-0344,Hydrazine Proposed Removal from Food Additive Use; Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-08-04T04:00:00Z,2014,8,2014-08-04T04:00:00Z,1979-08-14T03:59:59Z,2014-08-04T13:32:13Z,,0,0,090000648056e343
FDA-1978-N-0899-0025,FDA,FDA-1978-N-0899,Aflatoxins in Shelled Peanuts and Peanut Products Used as Human Foods; Proposed Tolerance: Reopening of Comment Period,Proposed Rule,Reopening of Comment Period,2014-07-31T04:00:00Z,2014,7,2014-07-31T04:00:00Z,1978-04-20T04:59:59Z,2014-08-01T01:04:57Z,,0,0,09000064817dede0
FDA-2014-F-0988-0001,FDA,FDA-2014-F-0988,BASF Corporation Filing of Food Additive Petition Animal Use,Proposed Rule,Petition,2014-07-25T04:00:00Z,2014,7,2014-07-25T04:00:00Z,2014-08-26T03:59:59Z,2014-07-28T12:39:58Z,2014-17458,0,0,09000064817e14ab
FDA-2014-N-0824-0001,FDA,FDA-2014-N-0824,"Confidentiality of Interim Results in Cardiovascular Outcome Safety Trials;
Public Hearing; Request for Comments",Proposed Rule,Public Hearing,2014-07-15T04:00:00Z,2014,7,2014-07-15T04:00:00Z,2014-10-11T03:59:59Z,2014-10-16T01:02:40Z,2014-16374,0,0,09000064817ad83d
FDA-2014-F-0232-0002,FDA,FDA-2014-F-0232,"Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use);
Correction",Proposed Rule,Correction,2014-07-08T04:00:00Z,2014,7,2014-07-08T04:00:00Z,2014-08-08T03:59:59Z,2014-07-08T15:05:07Z,2014-15761,0,0,0900006481796957
FDA-1999-N-0194-0001,FDA,FDA-1999-N-0194,"Additions and Modifications to the List of Drug Products That Have Been
Withdrawn or Removed From the Market for Reasons of Safety or
Effectiveness",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-07-02T04:00:00Z,2014,7,2014-07-02T04:00:00Z,2014-09-03T03:59:59Z,2024-09-20T19:06:15Z,2014-15371,0,0,0900006481787550
FDA-2014-N-0189-20870,FDA,FDA-2014-N-0189,"Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, as Amended by the Family Smoking Prevention and Tobacco Control Act; Regulations on the Sale and Distribution of Tobacco Products and Required Warning Statements for Tobacco Products; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2014-06-24T04:00:00Z,2014,6,2014-06-24T04:00:00Z,2014-08-09T03:59:59Z,2015-11-30T22:01:32Z,2014-14562,0,0,090000648175e473
FDA-2013-N-0590-0003,FDA,FDA-2013-N-0590,"Implementation of the Food and Drug Administration Food Safety
Modernization Act Amendments to the Reportable Food Registry Provisions of the Federal Food, Drug, and Cosmetic Act; Reopening of Comment Period",Proposed Rule,Reopening of Comment Period,2014-06-18T04:00:00Z,2014,6,2014-06-18T04:00:00Z,2014-08-19T03:59:59Z,2014-08-20T01:03:48Z,2014-14213,0,0,090000648174fb4f
FDA-2013-N-0195-0102,FDA,FDA-2013-N-0195,"Neurological Devices; Withdrawal of Proposed Effective Date of
Requirement for Premarket Approval for Cranial Electrotherapy Stimulator Devices",Proposed Rule,Withdrawal,2014-06-12T04:00:00Z,2014,6,2014-06-12T04:00:00Z,,2014-06-12T15:07:58Z,2014-13756,0,0,09000064817414fd
FDA-2011-N-0504-0190,FDA,FDA-2011-N-0504,"Neurological Devices; Withdrawal of Proposed Effective Date of
Requirement for Premarket Approval for Cranial Electrotherapy Stimulator Devices",Proposed Rule,Withdrawal,2014-06-12T04:00:00Z,2014,6,2014-06-12T04:00:00Z,,2014-06-12T15:03:32Z,2014-13756,0,0,0900006481740b58
FDA-2013-N-1529-0002,FDA,FDA-2013-N-1529,Medical Device Classification Procedures; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2014-06-12T04:00:00Z,2014,6,2014-06-12T04:00:00Z,2014-09-23T03:59:59Z,2014-12-24T17:10:11Z,2014-13705,0,0,0900006481740c73
FDA-1977-P-0006-0025,FDA,FDA-1977-P-0006,"Pasteurized Process Cheese and Cheese Prodcuts
Proposed Revision of Definitions and Standards of Identity; Proposed Rule",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-30T04:00:00Z,2014,5,2014-05-30T04:00:00Z,1978-01-04T04:59:59Z,2014-06-05T01:08:47Z,,0,0,09000064805d7d8e
FDA-2012-N-1210-0132,FDA,FDA-2012-N-1210,"Proposed Rules on Food Labeling: Revision of the Nutrition and
Supplement Facts Labels and Serving Sizes of Foods That Can Reasonably Be Consumed at One-Eating Occasion; Dual-Column Labeling; Updating, Modifying, and Establishing Certain Reference Amounts Customarily Consumed; Serving Size for Breath Mints; and Technical Amendments; Public Meeting",Proposed Rule,Public Meeting,2014-05-29T04:00:00Z,2014,5,2014-05-29T04:00:00Z,2014-08-02T03:59:59Z,2015-10-15T16:12:42Z,2014-12362,0,0,090000648171bb09
FDA-2014-N-0189-0932,FDA,FDA-2014-N-0189,"Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, as Amended by the Family Smoking Prevention and Tobacco Control Act; Regulations on the Sale and Distribution of Tobacco Products and Required Warning Statements for Tobacco Products; Correction",Proposed Rule,Correction,2014-05-28T04:00:00Z,2014,5,2014-05-28T04:00:00Z,,2017-08-08T18:28:46Z,2014-12296,0,0,09000064817189f4
FDA-2012-N-1210-0130,FDA,FDA-2012-N-1210,Food Labeling: Revision of the Nutrition and Supplement Facts Labels; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2014-05-27T04:00:00Z,2014,5,2014-05-27T04:00:00Z,2014-08-02T03:59:59Z,2015-10-07T15:37:42Z,2014-12094,0,0,090000648171527e
FDA-2004-N-0258-0048,FDA,FDA-2004-N-0258,"Food Labeling: Serving Sizes of Foods That Can Reasonably Be Consumed at One-Eating Occasion; Dual-Column Labeling; Updating, Modifying, and Establishing Certain Reference Amounts Customarily Consumed; Serving Size for Breath Mints; and Technical Amendments; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2014-05-27T04:00:00Z,2014,5,2014-05-27T04:00:00Z,2014-08-02T03:59:59Z,2015-06-12T01:30:23Z,2014-12095,0,0,09000064817153db
FDA-2013-N-0013-0026,FDA,FDA-2013-N-0013,"Sanitary Transportation of Human and Animal Food; Extension of Comment
Period",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-23T04:00:00Z,2014,5,2014-05-23T04:00:00Z,2014-07-31T03:59:59Z,2015-06-02T01:30:45Z,2014-12002,0,0,090000648170f1e2
FDA-2014-N-0440-0001,FDA,FDA-2014-N-0440,Microbiology Devices; Reclassification of Influenza Virus Antigen Detection Test Systems Intended for Use Directly With Clinical Specimens,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-22T04:00:00Z,2014,5,2014-05-22T04:00:00Z,2014-08-21T03:59:59Z,2014-08-21T01:03:49Z,2014-11635,0,0,090000648170c5a0
FDA-2014-N-0504-0001,FDA,FDA-2014-N-0504,"Administrative Destruction of Certain Drugs Refused Admission to the
United States",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-06T04:00:00Z,2014,5,2014-05-06T04:00:00Z,2014-07-08T03:59:59Z,2014-09-21T01:02:51Z,2014-10304,0,0,09000064816e416c
FDA-2014-N-0297-0001,FDA,FDA-2014-N-0297,"Reclassification of Surgical Mesh for Transvaginal Pelvic Organ Prolapse
Repair and Surgical Instrumentation for Urogynecologic Surgical Mesh
Procedures; Designation of Special Controls for Urogynecologic Surgical
Mesh Instrumentation",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-01T04:00:00Z,2014,5,2014-05-01T04:00:00Z,2014-07-31T03:59:59Z,2014-08-01T01:03:51Z,2014-09907,0,0,09000064816da464
FDA-2014-N-0298-0001,FDA,FDA-2014-N-0298,"Effective Date of Requirement for Premarket Approval for Surgical Mesh
for Transvaginal Pelvic Organ Prolapse Repair",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-01T04:00:00Z,2014,5,2014-05-01T04:00:00Z,2014-07-31T03:59:59Z,2014-07-31T01:59:28Z,2014-09909,0,0,09000064816da055
FDA-2014-F-0452-0001,FDA,FDA-2014-F-0452,"Novus International, Incorporated; Filing of Food Additive Petition
(Animal Use)",Proposed Rule,Petition,2014-04-25T04:00:00Z,2014,4,2014-04-25T04:00:00Z,2014-05-28T03:59:59Z,2014-05-13T14:36:45Z,2014-09406,0,0,09000064816cb33d
FDA-2014-N-0189-0001,FDA,FDA-2014-N-0189,"Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, as Amended by the Family Smoking Prevention and Tobacco Control Act; Regulations on the Sale and Distribution of Tobacco Products and Required Warning Statements for Tobacco Products",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-04-25T04:00:00Z,2014,4,2014-04-25T04:00:00Z,2014-07-10T03:59:59Z,2021-07-13T01:00:13Z,2014-09491,0,0,09000064816cb41a
FDA-2014-F-0469-0001,FDA,FDA-2014-F-0469,Excentials B.V.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-04-23T04:00:00Z,2014,4,2014-04-23T04:00:00Z,2014-05-24T03:59:59Z,2014-04-23T15:26:04Z,2014-09216,0,0,09000064816c3a3d
FDA-1995-N-0063-0024,FDA,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; Proposed Rule",Proposed Rule,General Notice,2014-04-22T04:00:00Z,2014,4,1996-07-09T04:00:00Z,1996-10-08T03:59:59Z,2014-06-16T13:08:40Z,,0,0,090000648056caeb
FDA-1991-N-0024-0008,FDA,FDA-1991-N-0024,Withdrawal of Certain Proposed Rules and Other Proposed Actions,Proposed Rule,Withdrawal,2014-04-10T04:00:00Z,2014,4,2014-04-10T04:00:00Z,,2014-04-10T19:50:14Z,,0,0,09000064805286ac
FDA-2014-F-0364-0001,FDA,FDA-2014-F-0364,Eastman Chemical Company; Filing of Food Additive Petition,Proposed Rule,Petition,2014-04-08T04:00:00Z,2014,4,2014-04-08T04:00:00Z,,2014-04-08T13:56:41Z,2014-07632,0,0,09000064816a7ddd
FDA-2013-N-1421-0001,FDA,FDA-2013-N-1421,"Guidance for Industry on What You Need To Know About Establishment,
Maintenance, and Availability of Records—Small Entity Compliance
Guide; Availability",Proposed Rule,GDL Guidance,2014-04-04T04:00:00Z,2014,4,2014-04-04T04:00:00Z,,2014-04-08T22:37:42Z,2014-07548,0,0,090000648169d850
FDA-2012-S-0782-0020,FDA,FDA-2012-S-0782,See  Document ID  FDA-2011-D-0674-0043 for the Correct Federal Register Document for Comment Participation,Proposed Rule,,2014-04-04T00:00:00Z,2014,4,,,2022-04-21T14:11:13Z,,0,1,090000648169d6db
FDA-2011-N-0179-0020,FDA,FDA-2011-N-0179,Draft Guidance for Industry: Prior Notice of Imported Food Questions and Answers (Edition 3); Availability,Proposed Rule,Notice of Availability,2014-03-31T04:00:00Z,2014,3,2014-03-31T04:00:00Z,2014-05-31T03:59:59Z,2014-05-31T01:08:17Z,2014-07046,0,0,0900006481691d03
FDA-2012-S-0782-0019,FDA,FDA-2012-S-0782,See  Document ID  FDA-2011-N-0179-0020 for the Correct Federal Register Document for Comment Participation,Proposed Rule,,2014-03-31T00:00:00Z,2014,3,,,2022-04-21T14:11:13Z,,0,1,0900006481691267
FDA-2013-N-0590-0001,FDA,FDA-2013-N-0590,"Implementation of the Food and Drug Administration Food Safety
Modernization Act Amendments to the Reportable Food Registry Provisions of the Federal Food, Drug, and Cosmetic Act",Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2014-03-26T04:00:00Z,2014,3,2014-03-26T04:00:00Z,2014-06-10T03:59:59Z,2014-07-17T01:02:56Z,2014-06614,0,0,0900006481681990
FDA-2014-F-0296-0001,FDA,FDA-2014-F-0296,DSM Nutritional Products; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-03-26T04:00:00Z,2014,3,2014-03-26T04:00:00Z,2014-04-26T03:59:59Z,2014-03-27T01:02:43Z,2014-06623,0,0,0900006481681a2a
FDA-2013-N-1529-0001,FDA,FDA-2013-N-1529,Medical Device Classification Procedures,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-03-25T04:00:00Z,2014,3,2014-03-25T04:00:00Z,2014-06-24T03:59:59Z,2014-06-21T01:04:55Z,2014-06364,0,0,090000648167c778
FDA-2013-N-1563-0002,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; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2014-03-25T04:00:00Z,2014,3,2014-03-25T04:00:00Z,2014-07-01T03:59:59Z,2014-07-02T01:06:29Z,2014-06469,0,0,090000648167c84d
FDA-2014-F-0295-0001,FDA,FDA-2014-F-0295,DSM Nutritional Products; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-03-25T04:00:00Z,2014,3,2014-03-25T04:00:00Z,2014-04-25T03:59:59Z,2014-03-25T14:05:01Z,2014-06487,0,0,090000648167c90d
FDA-2013-N-1425-0021,FDA,FDA-2013-N-1425,"Focused Mitigation Strategies To Protect Food Against Intentional
Adulteration; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2014-03-25T04:00:00Z,2014,3,2014-03-25T04:00:00Z,2014-07-01T03:59:59Z,2014-08-05T01:01:57Z,2014-06468,0,0,090000648167c911
FDA-2014-N-0108-0001,FDA,FDA-2014-N-0108,"New Animal Drug Applications; Confidentiality of Data and Information
in a New Animal Drug Application File",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-03-17T04:00:00Z,2014,3,2014-03-17T04:00:00Z,2014-06-03T03:59:59Z,2014-03-17T15:26:22Z,2014-05432,0,0,090000648166a8a8
FDA-2011-N-0921-0422,FDA,FDA-2011-N-0921,"Environmental Impact Statement for the Proposed Rule, Standards for
Growing, Harvesting, Packing, and Holding of Produce for Human
Consumption; Public Meeting on Scoping of Environmental Impact
Statement and Extension of Comment Period for Environmental Impact
Statement",Proposed Rule,Extension of Comment Period,2014-03-11T04:00:00Z,2014,3,2014-03-11T04:00:00Z,2014-04-19T03:59:59Z,2014-05-22T15:59:30Z,2014-05181,0,0,090000648165e239
FDA-2014-F-0232-0001,FDA,FDA-2014-F-0232,"Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use)",Proposed Rule,Petition,2014-03-10T04:00:00Z,2014,3,2014-03-10T04:00:00Z,2014-04-10T03:59:59Z,2014-03-10T17:23:36Z,2014-05066,0,0,090000648165aba4
FDA-2013-N-0745-0022,FDA,FDA-2013-N-0745,"Action Plan for the Collection, Analysis, and Availability of Demographic Subgroup Data in Applications for Approval of Food and Drug Administration-Regulated Medical Products; Notice of Public
Hearing; Request for Comments",Proposed Rule,Notice of Hearing,2014-03-04T05:00:00Z,2014,3,2014-03-04T05:00:00Z,2014-05-17T03:59:59Z,2014-05-18T01:02:23Z,2014-04625,0,0,09000064815f6b9f
FDA-2012-N-1210-0002,FDA,FDA-2012-N-1210,Food Labeling: Revision of the Nutrition and Supplement Facts Labels,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-03-03T05:00:00Z,2014,3,2014-03-03T05:00:00Z,2014-06-03T03:59:59Z,2025-12-05T10:00:12Z,2014-04387,1,0,09000064815f337c
FDA-2004-N-0258-0006,FDA,FDA-2004-N-0258,"Food Labeling: Serving Sizes of Foods That Can Reasonably Be Consumed at One-Eating Occasion; Dual-Column Labeling; Updating, Modifying, and Establishing Certain Reference Amounts Customarily Consumed; Serving Size for Breath Mints; and Technical Amendments",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-03-03T05:00:00Z,2014,3,2014-03-03T05:00:00Z,2014-06-03T03:59:59Z,2014-10-19T00:41:47Z,2014-04385,0,0,09000064815f3536
FDA-1994-P-0314-0003,FDA,FDA-1994-P-0314,"Food Labeling: Serving Sizes; Reference Amount and Serving Size
Declaration for Hard Candies, Breath Mints",Proposed Rule,Withdrawal,2014-03-03T05:00:00Z,2014,3,2014-03-03T05:00:00Z,,2014-03-03T15:34:57Z,2014-04386,0,0,09000064815f337e
FDA-2013-N-0402-0019,FDA,FDA-2013-N-0402,"Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives;
Public Hearing; Request for Comments",Proposed Rule,Notice of Hearing,2014-02-26T05:00:00Z,2014,2,2014-02-26T05:00:00Z,2014-06-14T03:59:59Z,2014-06-15T00:48:15Z,2014-03986,0,0,09000064815c3a9e
FDA-1996-P-0309-0024,FDA,FDA-1996-P-0309,Withdrawal of Certain Proposed Rules and Other Proposed Actions,Proposed Rule,Withdrawal,2014-02-20T05:00:00Z,2014,2,2014-02-20T05:00:00Z,,2014-02-20T12:41:16Z,,0,0,0900006480504ca5
FDA-2012-N-0378-0048,FDA,FDA-2012-N-0378,Physical Medicine Devices: Withdrawal of Proposed Effective Date of Requirement for Premarket Approval for Shortwave Diathermy for All Other Uses,Proposed Rule,Withdrawal,2014-02-20T05:00:00Z,2014,2,2014-02-20T05:00:00Z,,2014-02-24T16:31:38Z,2014-03593,0,0,09000064815906a1
FDA-1996-P-0309-0023,FDA,FDA-1996-P-0309,Withdrawal of Certain Proposed Rules and Other Proposed Actions; Notice of Intent,Proposed Rule,Withdrawal,2014-02-20T05:00:00Z,2014,2,2014-02-20T05:00:00Z,2003-07-22T03:59:59Z,2014-02-20T12:41:08Z,,0,0,0900006480504ca3
FDA-2012-N-0378-0049,FDA,FDA-2012-N-0378,"Physical Medicine Devices; Reclassification and Renaming of
Shortwave Diathermy for All Other Uses",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-02-20T05:00:00Z,2014,2,2014-02-20T05:00:00Z,2014-05-22T03:59:59Z,2015-06-12T01:30:53Z,2014-03594,0,0,0900006481590553
FDA-1996-P-0246-0024,FDA,FDA-1996-P-0246,Withdrawal of Certain Proposed Rules and Other Proposed Actions,Proposed Rule,Withdrawal,2014-02-20T05:00:00Z,2014,2,2014-02-20T05:00:00Z,,2014-02-20T14:37:39Z,,0,0,090000648050398a
FDA-2013-N-0013-0004,FDA,FDA-2013-N-0013,"Sanitary Transportation of Human and Animal Food; Public Meetings on
Proposed Rule",Proposed Rule,Public Meeting,2014-02-14T05:00:00Z,2014,2,2014-02-14T05:00:00Z,2014-02-15T04:59:59Z,2014-02-15T02:05:34Z,2014-03277,0,0,0900006481566206
FDA-2014-F-0149-0001,FDA,FDA-2014-F-0149,Lohmann Animal Health GMBH; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2014-02-10T05:00:00Z,2014,2,2014-02-10T05:00:00Z,2014-03-13T03:59:59Z,2014-03-13T01:04:09Z,2014-02725,0,0,09000064815562f1
FDA-2012-S-0782-0018,FDA,FDA-2012-S-0782,See  Document ID  FDA-2014-D-0033-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,Correction,2014-02-10T05:00:00Z,2014,2,2014-02-10T05:00:00Z,2014-03-28T03:59:59Z,2015-10-19T20:07:17Z,2014-02731,0,0,09000064815563e8
FDA-2012-S-0782-0017,FDA,FDA-2012-S-0782,See  Document ID  FDA-2014-0044-0001 for the Correct Federal Register Document for Comment Participation,Proposed Rule,,2014-02-10T00:00:00Z,2014,2,,,2022-04-21T14:11:13Z,,0,1,09000064815561fe
FDA-2013-N-0013-0001,FDA,FDA-2013-N-0013,Sanitary Transportation of Human and Animal Food,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-02-05T05:00:00Z,2014,2,2014-02-05T05:00:00Z,2014-06-01T03:59:59Z,2014-05-28T01:05:39Z,2014-02188,0,0,09000064815491f8
FDA-2013-N-1043-0002,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; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2014-02-03T05:00:00Z,2014,2,2014-02-03T05:00:00Z,2014-04-01T03:59:59Z,2014-04-06T02:34:03Z,2014-02112,0,0,0900006481542fe1
FDA-2011-N-0922-0019,FDA,FDA-2011-N-0922,"Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals; Extension of Comment
Period",Proposed Rule,Extension of Comment Period,2014-02-03T05:00:00Z,2014,2,2014-02-03T05:00:00Z,2014-04-01T03:59:59Z,2014-11-20T03:03:57Z,2014-02111,0,0,0900006481542fb1
FDA-2014-N-0113-0001,FDA,FDA-2014-N-0113,"Maximum Civil Money Penalty Amounts; Civil Money Penalty
Complaints",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-02-03T05:00:00Z,2014,2,2014-02-03T05:00:00Z,2014-04-22T03:59:59Z,2014-02-03T16:24:53Z,2014-02149,0,0,0900006481542dfb
FDA-2013-N-1425-0006,FDA,FDA-2013-N-1425,"Focused Mitigation Strategies To Protect Food Against Intentional
Adulteration; Public Meetings on Proposed Rule",Proposed Rule,Public Meeting,2014-01-31T05:00:00Z,2014,1,2014-01-31T05:00:00Z,,2014-01-31T15:11:58Z,2014-01985,0,0,0900006481539acd