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