documents
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76 rows where agency_id = "FDA", document_type = "Proposed Rule" and posted_year = 2015 sorted by posted_date descending
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| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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 | Sunlamp Products Performance Standard 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 | Exports: Notification and Recordkeeping requirements 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 | Exports: Notification and Recordkeeping requirements 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 | Requirements for Testing Human Blood Donors 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 | Revisions to Requirements to Blood,Blood Components & Plasma - CLOSED 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 | Licensed Anti-Human Globulin and Blood Grouping Reagents - CLOSED 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 | Disqualification of a Clinical Investigator 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 | Protection of Human subjects; Informed Consent 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 | Reference Daily Intake&Daily Reference Values/Food Labeling - CLOSED 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 | Bioterrorism Preparedness; Registration of Food Facilities 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 | Reference Daily Intake&Daily Reference Values/Food Labeling - CLOSED 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 | Bioengineered Foods Consumed By Humans or Animals 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 | Performance Standard for Diagnostic X-Ray Systems and Their Major Components 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 | Eligibility Criteria for Considering Additional Conditions in the Over-the-Counter Drug Monograph System 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 | Sunscreen Drug Products -OPEN 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 | Over-the-Counter Drug Products; Safety and Efficacy Review; Additional Sunscreen Ingredients 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 | Standard Identity for Cheese Product FD&C Yellow No. 6 & 5 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 | Standard Identity for Cheese Product FD&C Yellow No. 6 & 5 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 | Standard Identity for Cheese Product FD&C Yellow No. 6 & 5 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 |
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