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withdrawn,object_id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-2017-N-5476-0004,FDA,FDA-2017-N-5476,"Akzo Nobel Surface Chemistry AB; Filing of Food Additive Petition
(Animal Use); Reopening of the Comment Period",Proposed Rule,Reopening of Comment Period,2017-12-27T05:00:00Z,2017,12,2017-12-27T05:00:00Z,2018-01-27T04:59:59Z,2017-12-27T17:40:23Z,2017-27840,0,0,0900006482d76217
FDA-2017-F-4399-0006,FDA,FDA-2017-F-4399,Zinpro Corp.; Filing of Food Additive Petition (Animal Use); Reopening of the Comment Period,Proposed Rule,Request for Comment,2017-12-26T05:00:00Z,2017,12,2017-12-26T05:00:00Z,2018-01-26T04:59:59Z,2018-01-26T02:01:03Z,2017-27785,0,0,0900006482d727c2
FDA-2017-F-4375-0004,FDA,FDA-2017-F-4375,Akzo Nobel Surface Chemistry AB; Filing of Food Additive Petition (Animal Use); Reopening of the Comment Period,Proposed Rule,Request for Comment,2017-12-26T05:00:00Z,2017,12,2017-12-26T05:00:00Z,2018-01-26T04:59:59Z,2018-01-24T02:05:30Z,2017-27789,0,0,0900006482d72724
FDA-2017-N-6730-0001,FDA,FDA-2017-N-6730,"Center for Devices and Radiological Health; Medical Devices and 
Combination Products; Voluntary Malfunction Summary Reporting Program 
for Manufacturers",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-12-26T05:00:00Z,2017,12,2017-12-26T05:00:00Z,2018-02-27T04:59:59Z,2024-08-29T18:24:28Z,2017-27650,0,0,0900006482d7293c
FDA-2017-N-6502-0001,FDA,FDA-2017-N-6502,"Opioid Policy Steering Committee: Prescribing Intervention—Exploring a
Strategy for Implementation; Public Hearing; Request for Comments",Proposed Rule,Request for Comment,2017-12-13T05:00:00Z,2017,12,2017-12-13T05:00:00Z,2018-03-17T03:59:59Z,2018-03-17T13:01:10Z,2017-26785,0,0,0900006482d01ec1
FDA-2017-N-5095-0011,FDA,FDA-2017-N-5095,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-06T14:02:51Z,2017-26199,0,0,0900006482ce9c58
FDA-2017-N-5105-0005,FDA,FDA-2017-N-5105,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-09T02:02:36Z,2017-26199,0,0,0900006482ce8eed
FDA-2017-N-5094-0011,FDA,FDA-2017-N-5094,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-04-24T01:05:18Z,2017-26199,0,0,0900006482ce9c57
FDA-2017-N-5093-0007,FDA,FDA-2017-N-5093,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-06T14:02:16Z,2017-26199,0,0,0900006482ce9c55
FDA-2017-N-5092-0006,FDA,FDA-2017-N-5092,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-06T14:01:00Z,2017-26199,0,0,0900006482ce9d55
FDA-2017-N-5101-0007,FDA,FDA-2017-N-5101,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-06T14:03:57Z,2017-26199,0,0,0900006482ce9c5b
FDA-2017-N-5104-0005,FDA,FDA-2017-N-5104,"Review of Existing Regulatory and Information Collection Requirements;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2017-12-06T05:00:00Z,2017,12,2017-12-06T05:00:00Z,2018-02-06T04:59:59Z,2018-02-15T02:02:16Z,2017-26199,0,0,0900006482ce9c5d
FDA-2017-N-6538-0001,FDA,FDA-2017-N-6538,"Obstetrical and Gynecological Devices; Reclassification of Single-Use
Female Condom, To Be Renamed Single-Use Internal Condom",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-12-04T05:00:00Z,2017,12,2017-12-04T05:00:00Z,2018-02-03T04:59:59Z,2018-02-03T02:01:42Z,2017-26011,0,0,0900006482cd3c3c
FDA-2017-N-4919-0001,FDA,FDA-2017-N-4919,Medical Devices; Exemption From Premarket Notification: Class II Devices; Surgical Apparel; Request for Comments,Proposed Rule,Request for Comment,2017-11-30T05:00:00Z,2017,11,2017-11-30T05:00:00Z,2018-01-30T04:59:59Z,2018-01-30T02:03:35Z,2017-25781,0,0,0900006482cc0901
FDA-2017-N-6529-0001,FDA,FDA-2017-N-6529,"The Food and Drug Administration’s Approach To Evaluating Nicotine
Replacement Therapies; Public Hearing; Request for Comments",Proposed Rule,Request for Comment,2017-11-30T05:00:00Z,2017,11,2017-11-30T05:00:00Z,2018-02-16T04:59:59Z,2018-02-24T02:01:10Z,2017-25671,0,0,0900006482cc0a02
FDA-2017-C-6238-0001,FDA,FDA-2017-C-6238,"Colorcon, Inc.; Filing of Color Additive Petition",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-11-09T05:00:00Z,2017,11,2017-11-09T05:00:00Z,,2017-11-13T22:00:54Z,2017-24421,0,0,0900006482c60653
FDA-2011-F-0172-2718,FDA,FDA-2011-F-0172,Menu Labeling: Supplemental Guidance for Industry; Availability,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-11-09T05:00:00Z,2017,11,2017-11-09T05:00:00Z,2018-01-09T04:59:59Z,2018-01-09T14:00:37Z,2017-24246,0,0,0900006482c60715
FDA-2017-N-6216-0001,FDA,FDA-2017-N-6216,General Hospital and Personal Use Devices; Reclassification of Sharps Needle Destruction Device,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-11-07T05:00:00Z,2017,11,2017-11-07T05:00:00Z,2018-01-09T04:59:59Z,2017-11-18T14:00:24Z,2017-24191,0,0,0900006482c53fcd
FDA-2014-F-0295-0002,FDA,FDA-2014-F-0295,"DSM Nutritional Products, Inc.; Withdrawal of Food Additive Petition
(Animal Use)",Proposed Rule,Withdrawal,2017-11-01T04:00:00Z,2017,11,2017-11-01T04:00:00Z,,2017-11-01T14:20:54Z,2017-23728,0,0,0900006482c2e6eb
FDA-2013-F-1539-0005,FDA,FDA-2013-F-1539,"DSM Nutritional Products, Inc.; Withdrawal of Food Additive Petition
(Animal Use)",Proposed Rule,Withdrawal,2017-11-01T04:00:00Z,2017,11,2017-11-01T04:00:00Z,,2017-11-01T14:18:38Z,2017-23729,0,0,0900006482c2e6b3
FDA-2017-N-0763-0001,FDA,FDA-2017-N-0763,Food Labeling: Health Claims; Soy Protein and Coronary Heart Disease,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-10-31T04:00:00Z,2017,10,2017-10-31T04:00:00Z,2018-01-17T04:59:59Z,2018-02-01T02:04:19Z,2017-23629,0,0,0900006482c2875a
FDA-2011-N-0921-19151,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Compliance Dates for Subpart E;
Correction",Proposed Rule,Correction,2017-10-13T04:00:00Z,2017,10,2017-10-13T04:00:00Z,,2017-10-13T13:11:50Z,2017-22182,0,0,0900006482bc698e
FDA-1996-N-0114-0001,FDA,FDA-1996-N-0114,Radiology Devices; Proposed Classifications for Five Medical Image Management Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-10-06T04:00:00Z,2017,10,1996-12-02T05:00:00Z,1997-03-04T04:59:59Z,2017-10-06T16:41:55Z,96–30650,0,0,09000064804fe7c0
FDA-2012-N-1210-1302,FDA,FDA-2012-N-1210,"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; Proposed Extension of 
Compliance Dates",Proposed Rule,Notice of Extension,2017-10-02T04:00:00Z,2017,10,2017-10-02T04:00:00Z,2017-11-02T03:59:59Z,2018-02-24T02:04:22Z,2017-21019,0,0,0900006482b90039
FDA-2004-N-0258-0180,FDA,FDA-2004-N-0258,"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; Proposed Extension of 
Compliance Dates",Proposed Rule,Notice of Extension,2017-10-02T04:00:00Z,2017,10,2017-10-02T04:00:00Z,2017-11-02T03:59:59Z,2018-02-24T02:04:23Z,2017-21019,0,0,0900006482b9176a
FDA-2017-F-5528-0001,FDA,FDA-2017-F-5528,"Idemitsu Kosan, Cp. Ltd.; Filing of Food Additive Petition (Animal Use)",Proposed Rule,Correction,2017-09-25T04:00:00Z,2017,9,2017-09-25T04:00:00Z,,2017-09-25T13:12:53Z,2017-20385,0,0,0900006482b74efd
FDA-2017-F-4399-0001,FDA,FDA-2017-F-4399,Zinpro Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Amendment,2017-09-22T04:00:00Z,2017,9,2017-09-22T04:00:00Z,2017-10-24T03:59:59Z,2017-10-08T02:51:01Z,2017-20195,0,0,0900006482b6e6c3
FDA-2017-N-5476-0001,FDA,FDA-2017-N-5476,"Akzo Nobel Surface Chemistry AB; Filing of Food Additive Petition
(Animal Use)",Proposed Rule,Amendment,2017-09-21T04:00:00Z,2017,9,2017-09-21T04:00:00Z,2017-10-24T03:59:59Z,2017-09-28T01:03:52Z,2017-20062,0,0,0900006482b68ee0
FDA-2017-F-4375-0001,FDA,FDA-2017-F-4375,"Akzo Nobel Surface Chemistry AB; Filing of Food Additive Petition
(Animal Use)",Proposed Rule,Amendment,2017-09-21T04:00:00Z,2017,9,2017-09-21T04:00:00Z,2017-10-24T03:59:59Z,2017-09-22T01:02:33Z,2017-20049,0,0,0900006482b68f63
FDA-2017-F-4511-0001,FDA,FDA-2017-F-4511,"Arcadia Biosciences, Inc.; Filing of Food Additive Petition (Animal Use)",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-09-14T04:00:00Z,2017,9,2017-09-14T04:00:00Z,,2017-09-14T14:40:47Z,2017-19491,0,0,0900006482b34997
FDA-2011-N-0921-19144,FDA,FDA-2011-N-0921,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Compliance Dates for Subpart E",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-09-13T04:00:00Z,2017,9,2017-09-13T04:00:00Z,2017-11-14T04:59:59Z,2018-03-17T01:05:50Z,2017-19434,0,0,0900006482b2ce69
FDA-2017-N-5094-0001,FDA,FDA-2017-N-5094,Review of Existing Center for Food Safety and Applied Nutrition Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T14:01:04Z,2017-19030,0,0,0900006482b1792c
FDA-2017-N-5105-0001,FDA,FDA-2017-N-5105,Review of Existing Center for Devices and Radiological Health Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T02:03:46Z,2017-19034,0,0,0900006482b1792f
FDA-2017-N-5092-0001,FDA,FDA-2017-N-5092,Review of Existing Center for Biologics Evaluation and Research Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T02:02:04Z,2017-19032,0,0,0900006482b17927
FDA-2017-N-5093-0001,FDA,FDA-2017-N-5093,Review of Existing General Regulatory and Information Collection Requirements of Food and Drug Administration,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T02:01:06Z,2017-19047,0,0,0900006482b17929
FDA-2017-N-5104-0001,FDA,FDA-2017-N-5104,Review of Existing Center for Veterinary Medicine Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T02:04:10Z,2017-19031,0,0,0900006482b17a12
FDA-2017-N-5101-0001,FDA,FDA-2017-N-5101,Review of Existing Center for Drug Evaluation and Research Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T02:01:23Z,2017-19033,0,0,0900006482b17975
FDA-2017-N-5095-0001,FDA,FDA-2017-N-5095,Review of Existing Center for Tobacco Products Regulatory and Information Collection Requirements,Proposed Rule,Request for Comment,2017-09-08T04:00:00Z,2017,9,2017-09-08T04:00:00Z,2017-12-08T04:59:59Z,2017-12-08T14:01:08Z,2017-19035,0,0,0900006482b174ee
FDA-2017-F-3717-0002,FDA,FDA-2017-F-3717,Juice Products Association; Filing of Food Additive Petition; Correction,Proposed Rule,Correction,2017-08-22T04:00:00Z,2017,8,2017-08-22T04:00:00Z,,2017-08-22T13:22:53Z,2017-17704,0,0,0900006482a940ce
FDA-2017-F-3717-0001,FDA,FDA-2017-F-3717,Juice Products Association; Filing of Food Additive Petition,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-07-26T04:00:00Z,2017,7,2017-07-26T04:00:00Z,,2017-07-26T14:06:54Z,2017-15535,0,0,090000648296a013
FDA-2017-F-4125-0001,FDA,FDA-2017-F-4125,Zinpro Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-07-26T04:00:00Z,2017,7,2017-07-26T04:00:00Z,,2017-07-26T14:19:06Z,2017-15533,0,0,090000648296a65b
FDA-1989-N-0408-0001,FDA,FDA-1989-N-0408,General Biological Products Standards; Test for Residual Moisture,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-07-21T04:00:00Z,2017,7,1989-06-29T04:00:00Z,1989-08-29T03:59:59Z,2017-07-21T16:51:23Z,89-15356,0,0,090000648047a675
FDA-1992-N-0250-0001,FDA,FDA-1992-N-0250,Antiemetic Drug Products for Over-the-Counter Human Use; Proposed Amendment to the Monograph,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-06-30T04:00:00Z,2017,6,1993-08-26T04:00:00Z,1993-10-26T03:59:59Z,2024-03-26T11:31:23Z,93-20696,0,0,09000064805303e7
FDA-1995-N-0384-0001,FDA,FDA-1995-N-0384,Carcinogenicity Testing of Compounds Used in Food-Producing Animals,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-06-26T04:00:00Z,2017,6,1996-06-20T04:00:00Z,1996-09-04T03:59:59Z,2025-06-03T15:53:27Z,96–15725,0,0,090000648059a42b
FDA-2017-D-1105-0001,FDA,FDA-2017-D-1105,"Use of Electronic Records and Electronic Signatures in Clinical
Investigations Under Part 11— Questions and Answers; Draft
Guidance for Industry; Availability",Proposed Rule,Request for Comment,2017-06-21T04:00:00Z,2017,6,2017-06-21T04:00:00Z,2017-08-22T03:59:59Z,2017-08-22T13:48:40Z,2017-12811,0,0,0900006482711aad
FDA-2017-C-2902-0001,FDA,FDA-2017-C-2902,"Glo Eyes, LLC; Filing of Color Additive Petition",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-05-31T04:00:00Z,2017,5,2017-05-31T04:00:00Z,,2017-05-31T14:38:31Z,2017-11165,0,0,090000648266e608
FDA-2017-F-2130-0001,FDA,FDA-2017-F-2130,BASF Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-05-30T04:00:00Z,2017,5,2017-05-30T04:00:00Z,,2017-05-30T13:31:42Z,2017-11010,0,0,0900006482665ebc
FDA-1999-N-0195-0001,FDA,FDA-1999-N-0195,Amendment of Various Device Regulations to Reflect Current American Society for Testing and Materials Citations; Companion Document to Direct Final Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-05-15T04:00:00Z,2017,5,2000-01-24T05:00:00Z,2000-04-11T03:59:59Z,2024-10-29T14:45:14Z,00–1405,0,0,09000064804b0500
FDA-1984-N-0409-0003,FDA,FDA-1984-N-0409,Blackcurrant Juice; Termination of Consideration of Codex Standard,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2017-05-11T04:00:00Z,2017,5,1985-06-26T04:00:00Z,,2017-05-11T15:32:03Z,85-15281,0,0,09000064805aa73c
FDA-1984-N-0409-0001,FDA,FDA-1984-N-0409,Blackcurrant Juice; Advance Notice of Proposed Rulemaking on the Possible Establishment of a Standard,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2017-05-11T04:00:00Z,2017,5,1985-01-25T05:00:00Z,1985-03-27T04:59:59Z,2017-05-11T15:20:59Z,85-1883,0,0,09000064805aa73a
FDA-1999-N-4097-0001,FDA,FDA-1999-N-4097,Removal of Designated Journals; Companion Document to  Direct Final Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-05-09T04:00:00Z,2017,5,1999-12-10T05:00:00Z,2000-02-24T04:59:59Z,2024-09-30T20:37:04Z,99–31908,0,0,09000064804f5fc9
FDA-2015-F-0537-0027,FDA,FDA-2015-F-0537,"Natural Resources Defense Council et al.; Denial of Food Additive 
Petition",Proposed Rule,Denial,2017-05-04T04:00:00Z,2017,5,2017-05-04T04:00:00Z,2017-06-06T03:59:59Z,2017-06-06T13:02:09Z,2017-08987,0,0,09000064825909f4
FDA-1992-N-0146-0001,FDA,FDA-1992-N-0146,Labeling of Drug Products for Over·The-Counter Human Use; Technical Amendment,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-04-28T04:00:00Z,2017,4,1993-11-09T05:00:00Z,1994-01-11T04:59:59Z,2017-04-28T16:42:27Z,93-27509,0,0,090000648052e661
FDA-1996-N-0233-0001,FDA,FDA-1996-N-0233,Investigational Device Exemptions; Treatment Use,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-04-19T04:00:00Z,2017,4,1997-12-19T05:00:00Z,1997-01-28T04:59:59Z,2017-04-19T14:04:58Z,96-32186,0,0,090000648050375e
FDA-2017-F-0969-0001,FDA,FDA-2017-F-0969,Canadian Oilseed Processor Association; Filing of Food Additive Petition (Animal Use),Proposed Rule,Petition,2017-04-18T04:00:00Z,2017,4,2017-04-18T04:00:00Z,,2017-04-18T14:11:45Z,2017-07770,0,0,090000648255c2d5
FDA-2017-C-1951-0001,FDA,FDA-2017-C-1951,"Environmental Defense Fund, Earthjustice, Environmental Working
Group, Center for Environmental Health, Healthy Homes Collaborative,
Health Justice Project of Loyola University Chicago School of Law,
Breast Cancer Fund, Improving Kids’ Environment, Consumers Union,
Natural Resources Defense Council, Consumer Federation of America,
Learning Disabilities Association, Maricel Maffini, Howard Mielke",Proposed Rule,Petition,2017-04-04T04:00:00Z,2017,4,2017-04-04T04:00:00Z,2017-06-06T03:59:59Z,2017-06-06T01:01:35Z,2017-06581,0,0,0900006482539a73
FDA-2017-C-0935-0001,FDA,FDA-2017-C-0935,DSM Biomedical; Filing of Color Additive Petition,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-03-06T05:00:00Z,2017,3,2017-03-06T05:00:00Z,,2017-03-06T16:45:40Z,2017-04188,0,0,09000064824ee70f
FDA-2016-D-4120-0015,FDA,FDA-2016-D-4120,Fruit Juice and Vegetable Juice as Color Additives in Food; Draft Guidance for Industry; Reopening of Comment Period,Proposed Rule,Reopening of Comment Period,2017-03-01T05:00:00Z,2017,3,2017-03-01T05:00:00Z,2017-05-02T03:59:59Z,2017-05-02T01:00:55Z,2017-03929,0,0,09000064824e380f
FDA-1998-N-1172-0001,FDA,FDA-1998-N-1172,"Conforming Regulations Regarding Removal of Section 507 of the Federal Food, Drug, and Cosmetic Act; Companion Document to Direct Final Rule",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-02-16T05:00:00Z,2017,2,1999-01-05T05:00:00Z,1999-03-23T04:59:59Z,2024-08-22T20:15:46Z,99-141,0,0,09000064805a33ac
FDA-2016-D-2335-0843,FDA,FDA-2016-D-2335,Use of the Term ‘‘Healthy’’ in the Labeling of Human Food Products; Public Meeting; Request for Comments,Proposed Rule,Public Meeting,2017-02-16T05:00:00Z,2017,2,2017-02-16T05:00:00Z,2017-04-27T03:59:59Z,2022-09-29T13:02:04Z,2017-03117,0,0,09000064824c6883
FDA-1996-N-0468-0018,FDA,FDA-1996-N-0468,New Animal Drugs for Investigational Use and New Animal Drug Applications; Reopening of Comment Period,Proposed Rule,Reopening of Comment Period,2017-02-14T05:00:00Z,2017,2,1997-05-08T04:00:00Z,1997-06-10T03:59:59Z,2017-04-17T16:53:08Z,97-11845,0,0,09000064805079df
FDA-1996-N-0468-0001,FDA,FDA-1996-N-0468,New Animal Drugs for Investigational Use and New Animal Drug Applications,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2017-02-14T05:00:00Z,2017,2,1996-11-21T05:00:00Z,1997-01-22T04:59:59Z,2017-04-17T16:52:01Z,96–29767,0,0,09000064805079ce
FDA-1995-N-0306-0001,FDA,FDA-1995-N-0306,Maltodextrin; Food Chemicals Codex Specifications,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-02-10T05:00:00Z,2017,2,1995-09-21T04:00:00Z,1995-11-21T04:59:59Z,2024-07-15T20:14:41Z,95-23241,0,0,0900006480599a23
FDA-1995-N-0306-0003,FDA,FDA-1995-N-0306,Withdrawal of Certain Proposed Rules and Other Proposed Actions,Proposed Rule,Withdrawal,2017-02-10T05:00:00Z,2017,2,,,2024-07-16T12:47:52Z,04–26234,0,0,0900006480599a29
FDA-1995-P-0324-0003,FDA,FDA-1995-P-0324,"Lowfat and Skim Milk Products, Lowfat and Nonfat Yogurt Products, Lowfat Cottage Cheese: Proposed Revocation of Standards of Identity; Food Labeling, Nutrient Content Claims for Fat, Fatty Acids and Cholesterol Content of Food",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-02-03T05:00:00Z,2017,2,1995-11-09T05:00:00Z,1996-01-24T04:59:59Z,2017-02-04T02:02:44Z,95–27712,0,0,09000064824aad26
FDA-1995-N-0225-0001,FDA,FDA-1995-N-0225,Topical Antimicrobial Drug Products For Over-The-Counter Human Use; Proposed Amendment of Final Monograph for OTC First Aid Antibiotic Drug Products,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-02-01T05:00:00Z,2017,2,1996-02-14T05:00:00Z,1996-05-15T03:59:59Z,2024-07-30T14:48:31Z,96–3325,0,0,09000064805718b0
FDA-1995-P-0143-0005,FDA,FDA-1995-P-0143,"Lowfat and Skim Milk Products, Lowfat and Nonfat Yogurt Products, Lowfat Cottage Cheese: Proposed Revocation of  Standards of Identity; Food Labeling, Nutrient Content Claims for Fat, Fatty Acids and Cholesterol Content of Food",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-01-30T05:00:00Z,2017,1,1995-11-09T05:00:00Z,1996-01-24T04:59:59Z,2017-02-01T02:02:37Z,95–27712,0,0,090000648249f0bf
FDA-1995-P-0188-0003,FDA,FDA-1995-P-0188,"Lowfat and Skim Milk Products, Lowfat and Nonfat Yogurt Products, Lowfat Cottage Cheese: Proposed Revocation of Standards of Identity; Food Labeling, Nutrient Content Claims for Fat, Fatty Acids and Cholesterol Content of Food",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-01-27T05:00:00Z,2017,1,1995-11-09T05:00:00Z,1996-01-24T04:59:59Z,2024-05-30T21:42:07Z,95-27712,0,0,09000064824951b7
FDA-1995-P-0188-0023,FDA,FDA-1995-P-0188,Withdrawal of Certain Proposed Rules and Other Proposed Actions,Proposed Rule,Withdrawal,2017-01-27T05:00:00Z,2017,1,,,2017-01-27T16:43:09Z,04–26234,0,0,090000648056f8d1
FDA-2017-D-0175-0001,FDA,FDA-2017-D-0175,"Compliance With and Recommendations for Implementation of the 
Standards for the Growing, Harvesting, Packing, and Holding of Produce 
for Human Consumption for Sprout Operations; Draft Guidance for 
Industry; Availability",Proposed Rule,GDL Guidance,2017-01-23T05:00:00Z,2017,1,2017-01-23T05:00:00Z,2017-07-25T03:59:59Z,2017-07-25T13:06:36Z,2017-01128,0,0,0900006482488c31
FDA-2016-N-2527-0001,FDA,FDA-2016-N-2527,Tobacco Product Standard for N-Nitrosonornicotine Level in Finished Smokeless Tobacco Products,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2017-01-23T05:00:00Z,2017,1,2017-01-23T05:00:00Z,2017-04-11T03:59:59Z,2017-04-11T13:01:07Z,2017-01030,0,0,0900006482488bda
FDA-1995-N-0341-0001,FDA,FDA-1995-N-0341,Medical Devices; Reclassification and Codification of Rigid Gas Permeable Contact Lens Solution; Soft (Hydrophilic) Contact Lens Solution; and Contact Lens Heat Disinfecting Unit,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-01-23T05:00:00Z,2017,1,1996-04-01T05:00:00Z,1996-06-18T03:59:59Z,2025-06-02T23:01:47Z,96-7784,0,0,0900006480599dd3
FDA-1995-P-0281-0004,FDA,FDA-1995-P-0281,"Lowfat and Skim Milk Products, Lowfat and Nonfat Yogurt Products, Lowfat Cottage Cheese: Proposed Revocation of Standards of Identity; Food Labeling, Nutrient Content Claims for Fat, Fatty Acids and Cholesterol Content of Food",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-01-23T05:00:00Z,2017,1,1995-11-09T05:00:00Z,1996-01-24T04:59:59Z,2024-05-23T20:56:33Z,95–27712,0,0,0900006480598c92
FDA-2016-N-1149-0041,FDA,FDA-2016-N-1149,Manufacturer Communications Regarding Unapproved Uses of Approved or Cleared Medical Products; Availability of Memorandum; Reopening of the Comment Period,Proposed Rule,Reopening of Comment Period,2017-01-19T05:00:00Z,2017,1,2017-01-19T05:00:00Z,2017-04-20T03:59:59Z,2017-06-23T01:03:12Z,2017-01013,0,0,090000648248561c
FDA-2016-D-3401-0023,FDA,FDA-2016-D-3401,Scientific Evaluation of the Evidence on the Beneficial Physiological Effects of Isolated or Synthetic Non-Digestible Carbohydrates Submitted as a Citizen Petition; Draft Guidance for Industry; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2017-01-13T05:00:00Z,2017,1,2017-01-13T05:00:00Z,2017-02-14T04:59:59Z,2017-02-17T02:03:51Z,2017-00724,0,0,0900006482470477