dockets
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
5,000 rows where agency_id = "FDA" sorted by last_modified descending
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docket_type 2
- Nonrulemaking 4,932
- Rulemaking 68
agency_id 1
- FDA · 5,000 ✖
| id | agency_id | title | docket_type | last_modified ▲ | object_id |
|---|---|---|---|---|---|
| FDA-1991-N-0191 | FDA | Civil money penalties:biologics, drugs and medical devices | Nonrulemaking | 2026-02-27T22:02:58Z | 0b0000648052de46 |
| FDA-2000-M-0083 | FDA | DACS SC Kit (Density Gradient Separation Medium) | Nonrulemaking | 2026-02-27T15:28:34Z | 0b000064804b8053 |
| FDA-2000-C-0236 | FDA | Sodium Copper Chlorophyllin to Color Citrus Base Dry Beverage Mixes | Nonrulemaking | 2026-02-24T15:58:14Z | 0b000064804d5895 |
| FDA-2000-N-0012 | FDA | Request for Samples & Protocols; Agency Information Collection Activities | Nonrulemaking | 2026-02-24T15:55:19Z | 0b000064804ae876 |
| FDA-2000-M-0120 | FDA | PMA Defender II Model 9201 Implantable Cardioverter Defibrilator | Nonrulemaking | 2026-02-24T14:46:29Z | 0b000064804cf289 |
| FDA-2000-N-0046 | FDA | Importer's Entry Notice; Agency Information Collection Activities | Nonrulemaking | 2026-02-24T14:43:05Z | 0b000064804af15b |
| FDA-1981-N-0044 | FDA | HYDROGEN PEROXIDE AS GRAS | Nonrulemaking | 2026-02-24T14:29:07Z | 0b000064805af2fb |
| FDA-1997-S-0006 | FDA | Dietary Supplements, Courtesy Letters (Letters of Objection) | Nonrulemaking | 2026-02-20T19:22:56Z | 0b000064805c957d |
| FDA-2004-N-0451 | FDA | Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards | Nonrulemaking | 2026-02-19T15:23:46Z | 0b0000648047540d |
| FDA-2000-D-0104 | FDA | Conjugated Estrogens,USP-LC-MS Method for Qualitative Chemical | Nonrulemaking | 2026-02-17T14:20:25Z | 0b000064804c23c0 |
| FDA-2000-F-0166 | FDA | Components of Paper & Paperboard Incontact with Aqueous An | Nonrulemaking | 2026-02-17T11:53:41Z | 0b000064804d233a |
| FDA-2000-F-0056 | FDA | "Inhibitor of yeast", for the Safe of (DMDC) | Nonrulemaking | 2026-02-17T11:48:23Z | 0b000064804af591 |
| FDA-2000-F-0201 | FDA | Olestra Be Amended Requirement for Label Statement | Nonrulemaking | 2026-02-13T18:08:59Z | 0b000064804d47b7 |
| FDA-2000-V-1390 | FDA | Request for Variance for Laser Light Show | Nonrulemaking | 2026-02-13T18:04:52Z | 0b000064804f0e42 |
| FDA-2000-F-0055 | FDA | Safe Use for X-Radiation & Electron Beam Energy Sources | Nonrulemaking | 2026-02-13T15:47:36Z | 0b000064804af54b |
| FDA-2000-P-0184 | FDA | Totally Implanted Spinal Cord Stimulator | Nonrulemaking | 2026-02-13T15:44:16Z | 0b000064804d2a90 |
| FDA-2000-D-0067 | FDA | Medical Device Patient Labeling | Nonrulemaking | 2026-02-13T15:32:46Z | 0b000064804afceb |
| FDA-1981-N-0029 | FDA | Sodium Chloride GRAS Safety | Nonrulemaking | 2026-02-09T20:56:08Z | 0b000064805af08d |
| FDA-1985-P-0507 | FDA | ANDA SUIT RE: DIAZEPAM INTENSOL 5MG PER ML-CLOSED | Nonrulemaking | 2026-02-09T15:46:15Z | 0b000064805b79a1 |
| FDA-2003-D-0431 | FDA | Current Good Manufacturing Practices for Medical Gases | Nonrulemaking | 2026-02-03T20:46:43Z | 0b000064804a2255 |
| FDA-1995-S-0036 | FDA | Public Disclosure Materials for Emergency Research Studies Conducted Under 21 CFR 50.24 | Rulemaking | 2026-02-03T17:37:09Z | 0b0000648055af86 |
| FDA-2000-P-0211 | FDA | Amend the Product Insert and/or Label for Anthrax Vaccine Adsorbed | Nonrulemaking | 2026-02-03T15:25:23Z | 0b000064804d4c7c |
| FDA-2000-N-0222 | FDA | Dietary Supplement Health Claim/Implementation of Pearson Court Decision | Nonrulemaking | 2026-01-30T18:32:47Z | 0b000064804d51a5 |
| FDA-2000-P-0756 | FDA | ANADA Consisting of Different Physical Form of Drug Products | Nonrulemaking | 2026-01-30T18:22:34Z | 0b000064804e78ce |
| FDA-2000-P-0152 | FDA | Amend Part 133.3 Re: Milk & Nonfat Milk for Use in Standardization | Nonrulemaking | 2026-01-30T15:29:13Z | 0b000064804d1186 |
| FDA-2000-P-0414 | FDA | Prozac (Fluoxetine Hydrochloride) 20 mg Tablets Voluntarily Withdrawn | Nonrulemaking | 2026-01-30T15:25:11Z | 0b000064804daeec |
| FDA-2000-M-0203 | FDA | P990016; McCue CUBA Clinical Ultrasonic Bone Sonometry System | Nonrulemaking | 2026-01-30T14:58:36Z | 0b000064804d49d5 |
| FDA-2000-P-1064 | FDA | To Amend 21 CFR 107 Subpart B, Labeling of Infant Formulas | Nonrulemaking | 2026-01-26T14:08:58Z | 0b000064804ecd04 |
| FDA-2000-N-0048 | FDA | Technical Implementation of Electronic Records & Electronic Signatures | Nonrulemaking | 2026-01-23T14:19:52Z | 0b000064804af199 |
| FDA-2000-N-0165 | FDA | Parasitic Infections in United States as Result of Raw Fish Consumption | Nonrulemaking | 2026-01-23T14:16:11Z | 0b000064804d22bf |
| FDA-2000-N-1571 | FDA | Status of Useful Written Prescription Drug Information for Patients | Nonrulemaking | 2026-01-23T13:56:21Z | 0b00006480509235 |
| FDA-2004-P-0153 | FDA | Modification of 21 CFR Pt. 101.93 to Include Structure/Function ClaIms with Disclaimers that Eliminate Perceived Disease Connotations. | Nonrulemaking | 2026-01-22T14:14:09Z | 0b0000648046fff3 |
| FDA-1999-D-2955 | FDA | Impurities: Residual Solvents in New Veterinary Medicinal | Nonrulemaking | 2026-01-21T15:43:17Z | 0b000064804f26ac |
| FDA-2000-D-0420 | FDA | Potency Limits for Standardized Dust Mite & Grass | Nonrulemaking | 2026-01-13T14:10:40Z | 0b000064804db107 |
| FDA-2000-D-0160 | FDA | M4 Common Technical Document; International Conference on Harmonisation | Nonrulemaking | 2026-01-13T11:35:39Z | 0b000064804d1829 |
| FDA-2005-D-0460 | FDA | Guidance for industry on Pediatric Drug Development Under the Pediatric Research Equity Act and Qualifying for Pediatric Exclusivity Under the Best Pharmaceuticals for Children Act | Nonrulemaking | 2026-01-08T15:22:32Z | 0b00006480450aea |
| FDA-2000-P-0183 | FDA | Request that FDA Not Approve Upjohn's Bovine Growth Hormone | Nonrulemaking | 2026-01-06T18:45:26Z | 0b000064804d2a11 |
| FDA-2000-V-1073 | FDA | Class IIIb requirements for the IZLID Series Laser Products | Nonrulemaking | 2026-01-02T18:32:43Z | 0b000064804ed086 |
| FDA-2006-P-0207 | FDA | Petition for Review of Codex Standard for Honey Under 21 CFR 130.6 - OPEN | Nonrulemaking | 2026-01-02T14:33:19Z | 0b0000648045151f |
| FDA-2003-D-0143 | FDA | Part11, Electronic records, electronic signatures scope | Nonrulemaking | 2026-01-02T14:31:51Z | 0b00006480486504 |
| FDA-1998-D-0019 | FDA | Investigating out of Specification(OOS)Test Results fr Pharm | Nonrulemaking | 2026-01-02T14:26:42Z | 0b00006480563cc6 |
| FDA-2000-F-0115 | FDA | Stabilizer in Olefin Polymers/Safe Use in Food Contact | Nonrulemaking | 2025-12-19T13:47:19Z | 0b000064804cf0d1 |
| FDA-2000-N-0606 | FDA | Psychiatric & Behavioral Disturbances Associated w/Dementia | Nonrulemaking | 2025-12-19T13:31:02Z | 0b000064804dd979 |
| FDA-2000-N-0162 | FDA | Amendment of Regulations Regarding Certain Label Statement of Prescription Drugs | Nonrulemaking | 2025-12-19T13:21:00Z | 0b000064804d1924 |
| FDA-2000-D-0155 | FDA | Reprocessing & Reuse of Single-Use Devices/Risk Categorization | Nonrulemaking | 2025-12-16T14:25:22Z | 0b000064804d14c1 |
| FDA-2000-N-0191 | FDA | Reclassification of the Knee Joint Patellofemorotibal Metal | Nonrulemaking | 2025-12-16T12:26:32Z | 0b000064804d41a2 |
| FDA-2000-N-0106 | FDA | Exemption from Federal Preemption of State & Local Medical | Nonrulemaking | 2025-12-10T17:47:22Z | 0b000064804c2509 |
| FDA-1999-P-0001 | FDA | Reclassification and Codification of Absorbable Polydioxanone Surgical Suture | Nonrulemaking | 2025-12-09T13:24:03Z | 0b000064804a58b4 |
| FDA-1999-V-4085 | FDA | Variance Laser Light Show | Nonrulemaking | 2025-12-08T18:16:18Z | 0b000064804f5ecd |
| FDA-1999-P-1852 | FDA | Foods Derived from New Plant Varieties | Nonrulemaking | 2025-12-08T14:11:39Z | 0b000064804e7408 |
| FDA-2000-N-0108 | FDA | Safety Reporting Requirements Human Drug/Biological Products - CLOSED | Rulemaking | 2025-12-03T18:08:26Z | 0b000064804c262a |
| FDA-1999-D-0170 | FDA | Health Claims for Conventional Foods & Dietary Supplements | Nonrulemaking | 2025-12-02T14:33:32Z | 0b000064804b039e |
| FDA-1992-V-0040 | FDA | Laser effects for 'Fantasmic' show; CLOSED | Nonrulemaking | 2025-11-20T16:05:21Z | 0b00006480528933 |
| FDA-1999-D-0045 | FDA | Transmission of Zoonoses by Blood & Blood Products | Nonrulemaking | 2025-11-18T17:42:41Z | 0b000064804a5f5b |
| FDA-1999-P-0040 | FDA | Amend limit Hydrogenated & partially Hydrogenated Menhaden Oil | Nonrulemaking | 2025-11-18T14:53:35Z | 0b000064804a5d9b |
| FDA-1999-F-4617 | FDA | Food Safety & Inspection Service Safe Use of Ionizing Radiai | Nonrulemaking | 2025-11-18T14:17:27Z | 0b000064804f7562 |
| FDA-1986-P-0035 | FDA | EXCLUSIVE RIGHT TO DEPAKOTE (DIVALPROEX SODIUM)-CLOSED | Nonrulemaking | 2025-11-06T14:10:33Z | 0b0000648050e5c0 |
| FDA-1999-E-0090 | FDA | Patent Term Extension Application for Isolex 300 and ISOLEX 300i, U.S. Patent No. 4,714,680 | Nonrulemaking | 2025-11-04T18:21:28Z | 0b000064804a6a80 |
| FDA-1999-E-0123 | FDA | Patent Term Extension for Uvadex, U.S. Patent No. 4,999,375 | Nonrulemaking | 2025-11-04T18:17:51Z | 0b000064804ae990 |
| FDA-1999-F-4619 | FDA | Rubber Articles Intended for Use In Contact With Food | Nonrulemaking | 2025-11-04T18:03:59Z | 0b000064804f78db |
| FDA-1999-N-4097 | FDA | Removal of Designed Journals Companion Document | Nonrulemaking | 2025-10-28T14:21:33Z | 0b000064804f5fc5 |
| FDA-1999-N-0195 | FDA | Amendment of Various Device Regulations | Nonrulemaking | 2025-10-28T14:17:42Z | 0b000064804b04fa |
| FDA-1999-P-0151 | FDA | ANDA Suitability Petitions for Parenteral Drugs | Nonrulemaking | 2025-10-28T12:49:14Z | 0b000064804af144 |
| FDA-1999-P-0127 | FDA | ANDA for Sterile Cefuroxime Sodium, USP | Nonrulemaking | 2025-10-24T16:18:53Z | 0b000064804aea02 |
| FDA-1999-N-1323 | FDA | Redacted Version of Substantially-Equivalent Premarket Notification | Nonrulemaking | 2025-10-21T13:43:12Z | 0b000064804db076 |
| FDA-1999-P-4069 | FDA | ANDA for Naltrexone Hydrochloride Yablets for 25 100, &150mg | Nonrulemaking | 2025-10-21T13:09:35Z | 0b000064804f5e3f |
| FDA-1999-A-4057 | FDA | Advisory Opinion Oxine(stabilized Chlorine Dioxide) in Sweetwater Systems | Nonrulemaking | 2025-10-10T13:57:44Z | 0b000064804f572f |
| FDA-1999-P-4073 | FDA | ANDA for Propoxyphene Napsylate and Acetaminophen Tablets/Capsules 50mg | Nonrulemaking | 2025-10-10T13:10:26Z | 0b000064804f5e65 |
| FDA-1994-N-0415 | FDA | Proposal to Debar Robert E. Sacher, Ph.D. | Nonrulemaking | 2025-10-09T13:48:00Z | 0b0000648050882a |
| FDA-1999-P-2918 | FDA | Extend the Implementation Dates of the OTC Drug Labeling Rules | Nonrulemaking | 2025-10-07T16:14:50Z | 0b000064804f2302 |
| FDA-1999-D-0062 | FDA | New Use Food Contact Substance Notification Systems-Toxicolology | Nonrulemaking | 2025-10-07T11:13:07Z | 0b000064804a677c |
| FDA-1999-D-0066 | FDA | Sampling & Microbial Testing of Spent Irrigation Water | Nonrulemaking | 2025-09-30T12:59:56Z | 0b000064804a67c4 |
| FDA-2002-D-0188 | FDA | Nonclinical Studies for Development of Pharmaceutical Excipi | Nonrulemaking | 2025-09-24T16:24:59Z | 0b000064804957bb |
| FDA-1995-N-0389 | FDA | Fredrick Jay Shainfeld; Debarment Order | Nonrulemaking | 2025-09-24T16:24:23Z | 0b0000648059a4c9 |
| FDA-1998-D-0038 | FDA | Microbial Effects of Antimicrobial New Animal Drugs/Human Safety | Nonrulemaking | 2025-09-23T12:57:57Z | 0b00006480565cb1 |
| FDA-2005-P-0280 | FDA | To take the following actions with regard to aqueous-based drugs for inhalation that has been compounded by pharmacy operations | Nonrulemaking | 2025-09-23T12:35:31Z | 0b00006480444a54 |
| FDA-1999-F-0077 | FDA | Safe Use of Solid Solution | Nonrulemaking | 2025-09-23T11:20:23Z | 0b000064804a68d2 |
| FDA-1999-F-0056 | FDA | National Fisheries Institute and the Louisiana Department of Agriculture | Nonrulemaking | 2025-09-23T11:15:54Z | 0b000064804a61b4 |
| FDA-2000-D-0100 | FDA | Clinical Data In Marketing Applications | Nonrulemaking | 2025-09-22T15:08:05Z | 0b000064804c2118 |
| FDA-2003-D-0145 | FDA | Draft Guidance: Sterile Drug Products Produced by Aseptic Processing | Nonrulemaking | 2025-09-17T19:57:00Z | 0b00006480486926 |
| FDA-1999-M-0121 | FDA | PMA Medtronic Hancock II Bioprosthetic Heart Valve, Models T505, T510 & P980043 | Nonrulemaking | 2025-09-16T17:03:16Z | 0b000064804ae967 |
| FDA-1998-P-0083 | FDA | Withdrawn From Sale of Tylosterone Tablets | Nonrulemaking | 2025-09-10T18:33:30Z | 0b00006480584ac8 |
| FDA-2004-P-0212 | FDA | request the Commissioner of Food and Drugs to amend 21 CFR, Part 5.10) to request the Commissioner of Food and Drugs to amend 21 CFR, Part 101,subpart C: specific nutrition labeling requirements and guidelines, specifically nutrition labeling of dietary supplements 101.36(d)(1), to require the source of the dietary ingredient lycopene to be indentified as from tomato,fungus, or synthetic | Nonrulemaking | 2025-09-10T14:20:50Z | 0b000064804710ac |
| FDA-1999-H-0071 | FDA | Civil Money Penalty; Dong Seo Shin d/b/a East 4th Avenue Food Mart | Nonrulemaking | 2025-09-09T18:05:21Z | 0b000064804a6879 |
| FDA-1999-N-0031 | FDA | Positron Emmission Tomography Drug Products | Nonrulemaking | 2025-09-05T13:51:16Z | 0b000064804a5cdd |
| FDA-1999-P-2947 | FDA | Determine if Neurontin (Gabapentin) Tablets 600mg & 800 Have Withdrawn | Nonrulemaking | 2025-09-02T15:56:04Z | 0b000064804f2668 |
| FDA-1999-V-2946 | FDA | Laser Light Show Mobolazer | Nonrulemaking | 2025-09-02T14:26:18Z | 0b000064804f2660 |
| FDA-1999-P-0042 | FDA | Health Claim: Folic Acid, Vitamin B6 etc. & Vascular Disease | Nonrulemaking | 2025-09-02T10:56:24Z | 0b000064804a5e45 |
| FDA-1999-F-0020 | FDA | Benzenepropanoic Acid, 3-5-bis(1,1-dimethylethy)-4-hydroxy- | Nonrulemaking | 2025-08-29T13:57:43Z | 0b000064804a5ab2 |
| FDA-1999-F-0019 | FDA | Tridecanol Phosphite Butylidenebis[2-(1,-dimethylethy)-5-met | Nonrulemaking | 2025-08-29T13:54:21Z | 0b000064804a5aa1 |
| FDA-2002-D-0223 | FDA | Information for the use of Human Blood & Blood Components | Nonrulemaking | 2025-08-28T17:04:27Z | 0b00006480497176 |
| FDA-1999-F-0102 | FDA | Safe Use of Piperylene/2-methyl-2-butene/alpha-methylstyrene Terpolymers Use in Preparation of Can End Cements / Food Contact | Nonrulemaking | 2025-08-26T13:11:30Z | 0b000064804ae532 |
| FDA-2001-D-0197 | FDA | Statistical Approaches Establishing Bioequivalence | Nonrulemaking | 2025-08-15T13:34:50Z | 0b000064804e3068 |
| FDA-2002-N-0325 | FDA | Canned Tomatoes Deviating from Identity Standard | Nonrulemaking | 2025-08-14T14:35:19Z | 0b000064804a0b67 |
| FDA-2005-P-0319 | FDA | Withhold Approval of any ANDA or any 505(b)(2) Application for any Generic Version or Other Pharmaceutical Alternative of Venofer(Iron Sucrose Injection, USP) | Nonrulemaking | 2025-08-08T15:50:15Z | 0b00006480447df4 |
| FDA-2000-Q-0914 | FDA | Notification for Health Claims:Potassium Containing Foods | Nonrulemaking | 2025-08-08T12:10:26Z | 0b000064804e8b31 |
| FDA-2000-F-0147 | FDA | Safe use of ozone in gaseous & aqueous phases as antimicrobi | Nonrulemaking | 2025-08-08T12:09:19Z | 0b000064804d0f8c |
| FDA-1999-N-1876 | FDA | Blood Establishment Registration & Product Listing Form 2830 | Nonrulemaking | 2025-08-07T18:25:12Z | 0b000064804e767e |
| FDA-1999-F-2413 | FDA | Irradiate Animal Feeds/Feed Ingredients for Microbial Control | Nonrulemaking | 2025-08-01T18:10:18Z | 0b000064804f01c2 |
| FDA-1999-P-0091 | FDA | Adopt A Policy of Publicizing on the internet Certain Information | Nonrulemaking | 2025-08-01T16:35:47Z | 0b000064804a6a8d |
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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);