home / openregs

dockets

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

103 rows where agency_id = "FDA" and docket_type = "Rulemaking" sorted by last_modified descending

✎ View and edit SQL

This data as json, CSV (advanced)

Suggested facets: last_modified (date)

docket_type 1

  • Rulemaking · 103 ✖

agency_id 1

  • FDA · 103 ✖
id agency_id title docket_type last_modified ▲ object_id
FDA_FRDOC_0001 FDA Recently Posted FDA Rules and Notices. Rulemaking 2026-05-15T12:06:13Z 0b0000648039ac3c
FDA-2015-N-3469 FDA Bulk Drug Substances That Can Be Used To Compound Drug Products in Accordance With Section 503B of the Federal Food, Drug, and Cosmetic Act; Establishment of a Public Docket Rulemaking 2026-05-14T19:23:47Z 0b00006481ca7da5
FDA-1995-S-0036 FDA Public Disclosure Materials for Emergency Research Studies Conducted Under 21 CFR 50.24 Rulemaking 2026-05-13T13:49:22Z 0b0000648055af86
FDA-2008-N-0152 FDA Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Technical Amendment Rulemaking 2026-05-12T13:46:22Z 0b000064803e6ecb
FDA-2026-N-4659 FDA Medical Devices; Obstetrical and Gynecological Devices; Classification of the External Condom for Anal Intercourse or Vaginal Intercourse Rulemaking 2026-05-08T13:09:33Z 0b000064b92b25ae
FDA-2026-N-4645 FDA Medical Devices; Ophthalmic Devices; Classification of the Corneal Storage Medium With Preservatives Including Antifungals Rulemaking 2026-05-06T13:43:01Z 0b000064b92ad87b
FDA-2026-N-4644 FDA Medical Devices; Immunology and Microbiology Devices; Classification of the Device to Preserve and Stabilize Relative Abundances of Microbial Nucleic Acids in Clinical Samples Rulemaking 2026-05-06T13:36:42Z 0b000064b92ad877
FDA-2026-N-4643 FDA Medical Devices; Immunology and Microbiology Devices; Classification of the Circulating Tumor Cell Enrichment Device Rulemaking 2026-05-06T13:30:07Z 0b000064b92ac835
FDA-1996-N-0006 FDA Eligibility Criteria for Considering Additional Conditions in the Over-the-Counter Drug Monograph System Rulemaking 2026-05-01T14:17:00Z 0b000064804f9917
FDA-2026-N-4269 FDA Medical Devices; Neurological Devices; Classification of the Brain Temperature Measurement System Rulemaking 2026-04-30T13:34:43Z 0b000064b928c56c
FDA-2026-N-4270 FDA Medical Devices; Radiology Devices; Classification of the Radiation Therapy Marking Device Rulemaking 2026-04-30T13:29:28Z 0b000064b928af2b
FDA-2026-N-3946 FDA Medical Devices; Cardiovascular Devices; Classification of the Laser-Powered Inferior Vena Cava Filter Retrieval Catheter Rulemaking 2026-04-30T13:22:35Z 0b000064b9267937
FDA-2015-N-3534 FDA Bulk Drug Substances That Can Be Used To Compound Drug Products in Accordance With Section 503A of the Federal Food, Drug, and Cosmetic Act Rulemaking 2026-04-29T18:15:45Z 0b00006481cb06bd
FDA-2024-D-2977 FDA FDA Enforcement Policy for AAFCO-Defined Animal Feed Ingredients; Draft Guidance for Industry; Availability Rulemaking 2026-04-24T20:30:07Z 0b000064865c5781
FDA-2026-N-3930 FDA Medical Devices; Immunology and Microbiology Devices; Classification of the Alzheimer’s Disease Pathology Assessment Test Rulemaking 2026-04-22T12:42:49Z 0b000064b9265131
FDA-2026-N-3928 FDA Medical Devices; Ophthalmic Devices; Classification of the digital therapy device for amblyopia Rulemaking 2026-04-22T12:41:08Z 0b000064b9265112
FDA-2026-N-3929 FDA Medical Devices; Anesthesiology Devices; Classification of the Device for Sleep Apnea Testing Based on Mandibular Movement Rulemaking 2026-04-22T12:38:42Z 0b000064b9265116
FDA-2026-N-3900 FDA Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Setmelanotide Eligibility Gene Variant Detection System Rulemaking 2026-04-22T12:36:21Z 0b000064b9264ffd
FDA-2014-N-0189 FDA Deeming Tobacco Products To Be Subject to the 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 Rulemaking 2026-04-20T14:55:36Z 0b00006481554f10
FDA-2026-N-2959 FDA Medical Devices; Ear, Nose, and Throat Devices; Classification of the Transcutaneous Electrical Nerve Stimulator for the Relief of Congestion Rulemaking 2026-04-16T13:22:49Z 0b000064b922c445
FDA-2026-N-2887 FDA Medical Devices; Orthopedic Devices; Classification of the Manual Surgical Instrument for Appropriate Patient Selection for Orthopedic Implant Rulemaking 2026-04-16T13:12:39Z 0b000064b9225b28
FDA-1995-N-0259 FDA Regulations Restricting the Sale & Distribution of Cigarettes & Smokeless Tobacco to Protect Children & Adolescents Rulemaking 2026-04-14T14:44:56Z 0b00006480571c9d
FDA-2025-N-5996 FDA Medical Devices; Radiology Devices; Classification of Blood Irradiators Rulemaking 2026-04-09T14:39:48Z 0b000064b9075db9
FDA-2012-N-1210 FDA Food Labeling: Revision of the Nutrition and Supplement Facts Labels Rulemaking 2026-04-09T13:37:37Z 0b00006481185d17
FDA-2024-C-1085 FDA Phytolon Ltd; Filing of Color Additive Petition Rulemaking 2026-04-02T15:01:13Z 0b00006486457d5c
FDA-2025-N-5995 FDA Effective Date of Requirement for Premarket Approval Applications for Blood Irradiators Intended to Prevent Metastasis Rulemaking 2026-03-26T16:49:40Z 0b000064b9075b4e
FDA-2015-N-0101 FDA Safety and Effectiveness for Health Care Antiseptics; Topical Antimicrobial Drug Products for Over-the-Counter Human Use Rulemaking 2026-03-18T14:32:02Z 0b000064819b0578
FDA-2000-N-0108 FDA Safety Reporting Requirements Human Drug/Biological Products Rulemaking 2026-03-17T12:00:53Z 0b000064804c262a
FDA-2015-N-1765 FDA General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products Rulemaking 2026-03-16T13:19:20Z 0b00006481ae5abf
FDA-2024-N-2910 FDA Food Labeling: Front-of-Package Nutrition Information Rulemaking 2026-03-12T15:38:51Z 0b000064865bd26a
FDA-2000-N-0044 FDA Labeling for Human Prescription Drug/Biologic Products Rulemaking 2026-03-06T18:10:25Z 0b000064804aefdb
FDA-2021-N-1351 FDA Revising the National Drug Code Format and Drug Label Barcode Requirements Rulemaking 2026-03-05T14:56:05Z 0b00006484ee7222
FDA-2011-N-0179 FDA Information Required in Prior Notice of Imported Food Rulemaking 2026-02-25T13:54:39Z 0b00006480c0d540
FDA-2020-N-1383 FDA Revocation of Methods of Analysis Regulation Rulemaking 2026-02-23T17:57:31Z 0b000064845eacc2
FDA-2024-N-4016 FDA Revocation of Regulations Regarding the Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and The European Community Rulemaking 2026-02-23T17:56:00Z 0b0000648665d84e
FDA-2015-N-0030 FDA Compounding of Human Drug Products Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act; Establishment of a Public Docket Rulemaking 2026-02-18T14:17:55Z 0b000064819a3b34
FDA-2008-P-0086 FDA Cheeses & Related Cheese Products; Proposal to Permit the Use of Ultrafiltered Milk; Extension of the Comment Period Rulemaking 2026-01-30T15:36:20Z 0b000064803a81eb
FDA-2007-0629 FDA Cheeses & Related Cheese Products; Proposal to Permit the Use of Ultrafiltered Milk; Reopening of the Comment Period Rulemaking 2026-01-30T15:33:08Z 0b000064803779c9
FDA-2025-N-4622 FDA Immunology and Microbiology Devices; Reclassification of Nucleic Acid-Based Test Systems for Use with a Corresponding Approved Oncology Therapeutic Product Rulemaking 2026-01-28T17:58:22Z 0b000064b8fedfa1
FDA-2012-D-1002 FDA Questions and Answers Regarding Food Facility Registration Rulemaking 2026-01-27T18:17:19Z 0b0000648111f41d
FDA-2000-N-0011 FDA Uniform Compliance Date for Food Labeling Regulations Rulemaking 2025-03-05T10:39:56Z 0b000064804ae7d6
FDA-1978-N-0018 FDA Sunscreen Drug Products -OPEN Rulemaking 2025-01-22T08:25:01Z 0b00006480559264
FDA-1975-N-0012 FDA Health Care Antiseptic Drug Products for Over-the-Counter (OTC) Human Use; CLOSED Rulemaking 2024-05-24T10:11:19Z 0b000064805c1903
FDA-2006-N-0239 FDA Index of Legally Marketed Unapproved New Animal Drugs for Minor Species Rulemaking 2024-05-15T09:29:00Z 0b00006480456e9e
FDA-2003-F-0321 FDA Creamers for Use in Alcoholic Beverages Rulemaking 2023-10-13T14:23:03Z 0b00006480495779
FDA-1992-S-0039 FDA Public Docket to Provide Information on Submissions the Agency is Prepared to Accept Electronically Rulemaking 2023-07-21T16:50:48Z 0b00006480528808
FDA-2000-P-0126 FDA Revision of Yogurt Standards Rulemaking 2023-05-19T08:27:18Z 0b000064804cf4c3
FDA-1998-N-0051 FDA Over the Counter Human Drugs Labeling Requirements Rulemaking 2023-04-17T17:42:05Z 0b0000648056e834
FDA-2001-N-0178 FDA Performance Standard for Diagnostic X-Ray Systems and Their Major Components Rulemaking 2023-02-22T09:25:21Z 0b000064804e14e6
FDA-1997-N-0020 FDA Substances Generally Recognized as Safe (GRAS) - Closed Rulemaking 2022-01-05T01:02:36Z 0b000064805ca0a0
FDA-1975-N-0016 FDA OTC Topical Antimicrobial Drug Products - OPEN Rulemaking 2022-01-05T01:02:28Z 0b000064805c1f98
FDA-1975-N-0013 FDA First Aid; Topical Antimicrobial Drug Products for Over-the-Counter (OTC) Human Use (OPEN) Rulemaking 2022-01-05T01:02:27Z 0b000064805c1d37
FDA-1995-N-0063 FDA CGMPs for the Production of Infant Formula Rulemaking 2022-01-05T01:02:26Z 0b0000648056ca61
FDA-2003-N-0196 FDA Over-the-Counter Drug Products; Safety and Efficacy Review; Additional Sunscreen Ingredients Rulemaking 2022-01-05T01:02:18Z 0b0000648048b48b
FDA-2005-N-0345 FDA Distribution of Blood Derivatives by Registered Blood Establishments that Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements and Administrative Procedures (Section 610 Review) Rulemaking 2022-01-05T01:02:18Z 0b00006480449858
FDA-2005-N-0404 FDA Food Labeling; Gluten-Free Labeling of Foods-CLOSED Rulemaking 2022-01-05T01:02:18Z 0b0000648044d3d3
FDA-1988-N-0019 FDA Prescription Drug Marketing Act of 1987 Rulemaking 2022-01-05T01:02:16Z 0b00006480475d46
FDA-1992-N-0407 FDA Prescription Drug Amendments of 1992; Ltr to Regulated Industy Rulemaking 2022-01-05T01:01:39Z 0b00006480532581
FDA-1977-N-0320 FDA Protein Supplements-RETIRED Rulemaking 2021-09-01T18:06:30Z 0b000064805ee043
FDA-1977-N-0259 FDA Cultured & Acidified Buttermilk, Yogurts, Milks & Eggnog - OPEN Rulemaking 2021-09-01T18:06:29Z 0b000064805ed178
FDA-1997-D-0494 FDA Direct Final Rule Procedures Rulemaking 2021-09-01T18:06:15Z 0b000064805d46c6
FDA-1980-N-0004 FDA Over-the-Counter Ophthalmic Drug Products for Emergency First Aid Use; Proposed Amendment of Final Monograph for Over-the-Counter Opthalmic Drug Products Rulemaking 2021-09-01T18:05:33Z 0b000064805b9002
FDA-1985-C-0553 FDA Canthaxanthin; Color Additive Exemtp From Ccertification Rulemaking 2021-09-01T18:05:32Z 0b000064805b7c5a
FDA-1981-N-0293 FDA Standards of Identity for Milk, Lowfat Milk & Skim Milk Pasteurized Rulemaking 2021-09-01T18:05:12Z 0b000064805b0e91
FDA-1981-N-0114 FDA Topical Acne Drug Product For Over-the-Counter Human Use Rulemaking 2021-09-01T18:05:07Z 0b000064805b0529
FDA-1978-N-1975 FDA Red Cell Lysing Reagents -RETIRED Rulemaking 2021-09-01T18:04:31Z 0b000064805a1aa4
FDA-1978-N-1713 FDA Blood & Plasma Warming Devices-RETIRED Rulemaking 2021-09-01T18:04:17Z 0b0000648059cab9
FDA-1978-N-1451 FDA Blood Cell Diluents-RETIRED Rulemaking 2021-09-01T18:04:04Z 0b0000648059b436
FDA-1978-N-1463 FDA Processing Systems for Frozen Blood-RETIRED Rulemaking 2021-09-01T18:04:04Z 0b0000648059b4f7
FDA-1978-N-1177 FDA Calibrators for Platelet Counting-RETIRED Rulemaking 2021-09-01T18:03:42Z 0b000064805984f6
FDA-1978-N-0924 FDA Thrombin Time Test-RETIRED Rulemaking 2021-09-01T18:03:29Z 0b0000648058dadc
FDA-1978-N-0925 FDA Calibrators for Cell Indices-RETIRED Rulemaking 2021-09-01T18:03:29Z 0b0000648058dbd3
FDA-1998-N-0155 FDA Treatment of Narcotic Dependence Rulemaking 2021-09-01T18:03:27Z 0b0000648058b15e
FDA-1978-N-0635 FDA Empty Containers for the Collection & Processing of Blood-RETIRED Rulemaking 2021-09-01T18:03:18Z 0b00006480579244
FDA-1978-N-0622 FDA Calibrators for Red Cell & White Cell Counting Rulemaking 2021-09-01T18:03:17Z 0b00006480578721
FDA-1978-N-0624 FDA Medical Devices Classification of Prothrombin-Proconvertin Tests and Thrombotests-RETIRED Rulemaking 2021-09-01T18:03:17Z 0b0000648057895b
FDA-1978-N-0625 FDA Partial Thromboplastin Time Tests-RETIRED Rulemaking 2021-09-01T18:03:17Z 0b00006480578a8f
FDA-1978-N-0632 FDA Thromboplastin Generation Test-RETIRED Rulemaking 2021-09-01T18:03:17Z 0b00006480579019
FDA-1978-N-0633 FDA Automated Blood Grouping & Antibody Test Systems-RETIRED Rulemaking 2021-09-01T18:03:17Z 0b00006480579087
FDA-1978-N-0375 FDA Medical Devices Classification of Prothrombin Time Tests-RETIRED Rulemaking 2021-09-01T18:03:06Z 0b0000648056e729
FDA-1978-N-0379 FDA Classification of Blood Mixing Devices & Blood Weighing Devices-RETIRED Rulemaking 2021-09-01T18:03:06Z 0b0000648056e7dd
FDA-1978-N-0380 FDA Automated Blood Cell Separators-RETIRED Rulemaking 2021-09-01T18:03:06Z 0b0000648056e7f7
FDA-1978-N-0381 FDA Automated Cell Washing Centrifuges for Immuno-Hematology-RETIRED Rulemaking 2021-09-01T18:03:06Z 0b0000648056e829
FDA-1978-N-0382 FDA Automated Coombs Test Systems-RETIRED Rulemaking 2021-09-01T18:03:06Z 0b0000648056e83b
FDA-1978-N-0368 FDA Hematology Stains-RETIRED Rulemaking 2021-09-01T18:03:05Z 0b0000648056e64a
FDA-1978-N-0123 FDA Hematology Quality Control Mixtures Rulemaking 2021-09-01T18:02:55Z 0b00006480564674
FDA-1978-N-0124 FDA Russell Viper Venom Reagent - RETIRED Rulemaking 2021-09-01T18:02:55Z 0b00006480564725
FDA-1978-N-0115 FDA Calibrators for Hemoglobin & Hematocrit Measurement-RETIRED Rulemaking 2021-09-01T18:02:54Z 0b00006480564113
FDA-1978-N-0061 FDA Hematology and Pathology Devices Classification of Sickle Cell Tests-RETIRED Rulemaking 2021-09-01T18:02:53Z 0b000064805622ba
FDA-1978-N-0023 FDA Skin Bleaching Drug Products- OPEN Rulemaking 2021-09-01T18:02:51Z 0b0000648055ed99
FDA-1995-G-0034 FDA Hydrophobic Silica for Animal Feeds-CLOSED Rulemaking 2021-09-01T18:02:51Z 0b0000648055add9
FDA-1979-N-0424 FDA Labels of Drug & Cosmetic Products-RETIRED Rulemaking 2021-09-01T18:02:48Z 0b0000648055648a
FDA-1979-N-0028 FDA Lakes of Color Additives Rulemaking 2021-09-01T18:02:36Z 0b0000648055395f
FDA-1992-N-0190 FDA Standard Identity for Cheese Product FD&C Yellow No. 6 & 5 Rulemaking 2021-09-01T18:02:09Z 0b0000648052f609
FDA-1992-N-0049 FDA Topical Drug Containing Benzoyl Peroxide; Additional Labeling Rulemaking 2021-09-01T18:01:56Z 0b0000648052bcdf
FDA-1990-N-0025 FDA Food Labeling, Declaration of Ingredients Rulemaking 2021-09-01T18:01:53Z 0b0000648052957f
FDA-1982-F-0155 FDA Direct Food Additives: Food Additives Permitted for Direct Addition to Food for Human Consuption; Dimethyl Dicarbonate Rulemaking 2021-09-01T18:01:19Z 0b0000648050f5f7
FDA-1996-N-0027 FDA National Environmental Policy Act Proposed Revision of Policies and Procedures Rulemaking 2021-09-01T18:00:26Z 0b000064804fb548
FDA-2002-N-0323 FDA Bioterrorism Preparedness; Registration of Food Facilities Rulemaking 2021-09-01T01:03:15Z 0b000064804a02e5
FDA-2002-N-0031 FDA Animal Proteins Prohibited in Ruminant Feed Rulemaking 2021-09-01T01:02:59Z 0b00006480489512

Next page

Advanced export

JSON shape: default, array, newline-delimited, object

CSV options:

CREATE TABLE dockets (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    title TEXT,
    docket_type TEXT,
    last_modified TEXT,
    object_id TEXT
);
CREATE INDEX idx_dockets_agency ON dockets(agency_id);
CREATE INDEX idx_dockets_type ON dockets(docket_type);
Powered by Datasette · Queries took 118.652ms · Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API