documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
1,549 rows where document_type = "Notice" and posted_year = 2025 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| EPA_FRDOC_0001-32454 | EPA | EPA_FRDOC_0001 | No-Migration Variance from Land Disposal Restrictions for Clean Harbors Lone Mountain, OK | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T18:49:21Z | C1-2025-22553 | 0 | 0 | 09000064b910c3ea | ||
| EPA-HQ-OAR-2021-0329-0065 | EPA | Proposed Information Collection Request; Comment Request; Certification and Compliance Requirements for Nonroad Spark-Ignition Engines (Renewal), ICR 1695.14, OMB 2060-0338 EPA-HQ-OAR-2021-0329 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Certification and Compliance Requirements for Nonroad Spark-Ignition Engines | Notice | Information Collection Request (ICR) | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-29T04:59:59Z | 2026-01-17T13:22:17Z | 2025-23922 | 0 | 0 | 09000064b910c3e7 |
| EPA-HQ-OPPT-2021-0728-0032 | EPA | EPA-HQ-OPPT-2021-0728 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: TSCA Section 5 Premanufacture Review of New Chemical Substances and Significant New Use Rules for New and Existing Chemical Substances (Renewal) | Notice | Information Collection Request (ICR) | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2025-12-30T19:39:06Z | 2025-23972 | 0 | 0 | 09000064b910c4eb |
| EPA-HQ-OLEM-2018-0646-0046 | EPA | Safe Management of Recalled Airbags EPA-HQ-OLEM-2018-0646 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Safe Management of Recalled Airbags Rule | Notice | Information Collection Request (ICR) | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2025-12-30T19:16:12Z | 2025-23973 | 0 | 0 | 09000064b910c3e6 |
| EPA-HQ-OAR-2020-0657-0005 | EPA | NSPS for Kraft Pulp Mills (40 CFR Part 60, Subpart BB) (Renewal) EPA-HQ-OAR-2020-0657 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: New Source Performance Standards for Kraft Pulp Mills | Notice | Information Collection Request (ICR) | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2025-12-30T19:28:24Z | 2025-23966 | 0 | 0 | 09000064b910d14d |
| EPA-HQ-OAR-2022-0066-0004 | EPA | NSPS for Grain Elevators (40 CFR Part 60, Subpart DD) (Renewal) EPA-HQ-OAR-2022-0066 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: New Source Performance Standards for Grain Elevators | Notice | Information Collection Request (ICR) | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2025-12-30T19:45:22Z | 2025-23921 | 0 | 0 | 09000064b910c4ee |
| EPA-HQ-OPP-2020-0693-0026 | EPA | EPA-HQ-OPP-2020-0693 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Pesticide Data Call-Ins | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2025-12-31T00:15:34Z | 2025-23967 | 0 | 0 | 09000064b910c441 | |
| FDA-2025-N-1928-0026 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1250 - Alternansucrase enzyme preparation produced by Escherichia coli | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:09:02Z | 0 | 0 | 09000064b910d339 | ||
| FDA-2025-N-1928-0033 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1278 - Lactiplantibacillus plantarum CGMCC 6312 | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:17:03Z | 0 | 0 | 09000064b910d360 | ||
| FDA-2025-N-1928-0031 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1273 - Lacto-N-tetraose | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:15:50Z | 0 | 0 | 09000064b910d33f | ||
| FDA-2025-N-1928-0032 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1276 - Cellulase enzyme preparation produced by Trichoderma reesei | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:16:15Z | 0 | 0 | 09000064b910d340 | ||
| FDA-2025-N-1928-0029 | FDA | FDA-2025-N-1928 | GRAS Notice GRN 1269 - Modified monellin preparation produced by Komagataella phaffii CBS 150005 - Part 1 of 2 | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:12:21Z | 0 | 0 | 09000064b910d33d | ||
| FDA-2025-N-1927-0099 | FDA | FDA-2025-N-1927 | GRAS Notice (GRN) 1226 - Orange (Citrus sinensis) extract - amendments | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:07:43Z | 0 | 0 | 09000064b910d2f3 | ||
| FDA-2025-N-1928-0027 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1266 - Wheat fiber extract from wheat (Triticumaestivum) | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:10:03Z | 0 | 0 | 09000064b910d33a | ||
| FDA-2025-N-1928-0028 | FDA | FDA-2025-N-1928 | GRAS Notice (GRN) 1267 - Sunflower lecithin | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:10:59Z | 0 | 0 | 09000064b910d33b | ||
| FDA-2025-N-1928-0030 | FDA | FDA-2025-N-1928 | GRAS Notice GRN 1269 - Modified monellin preparation produced by Komagataella phaffii CBS 150005 - Part 2 of 2 | Notice | General Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T23:15:10Z | 0 | 0 | 09000064b910d33e | ||
| FWS-R8-ES-2025-0407-0001 | FWS | Receipt of Incidental Take Permit Application and Proposed Habitat Conservation Plan for Piraeus Point Project, City of Encinitas, CA; Categorical Exclusion FWS-R8-ES-2025-0407 | Receipt of Incidental Take Permit Application and Proposed Habitat Conservation Plan for Piraeus Point Project, City of Encinitas, CA; Categorical Exclusion | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2026-01-30T04:59:59Z | 2026-01-31T13:12:40Z | 2025-23971 | 0 | 0 | 09000064b910c358 | |
| USDA_FRDOC_0001-3252 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Agency Information Collection Activities; Proposals, Submissions, and Approvals | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T18:50:04Z | 2025-24006 | 0 | 0 | 09000064b910d1dd | ||
| USDA_FRDOC_0001-3250 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Agency Information Collection Activities; Proposals, Submissions, and Approvals | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T18:49:32Z | 2025-23982 | 0 | 0 | 09000064b910c448 | ||
| USDA_FRDOC_0001-3251 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Agency Information Collection Activities; Proposals, Submissions, and Approvals | Notice | 2025-12-30T05:00:00Z | 2025 | 12 | 2025-12-30T05:00:00Z | 2025-12-30T18:50:02Z | 2025-23981 | 0 | 0 | 09000064b910d199 | ||
| EPA-R09-OAR-2025-4149-0001 | EPA | EPA-R09-OAR-2025-4149 | Receipt of Tribal Minor NSR Permit Application for Morongo Casino Cogeneration Facility | Notice | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2025-12-30T04:48:22Z | 0 | 0 | 09000064b910c58d | |||
| FDA-2025-N-7022-0001 | FDA | FDA-2025-N-7022 | Roundtable on Premarket Tobacco Application Submissions for Electronic Nicotine Delivery Systems Products; Notice of Meeting; Establishment of a Public Docket; Request for Comments | Notice | Request for Comments | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-03-13T03:59:59Z | 2026-02-14T13:17:33Z | 2025-23851 | 1 | 0 | 09000064b910a287 |
| FDA-2024-E-1284-0008 | FDA | FDA-2024-E-1284 | Determination of Regulatory Review Period for Purposes of Patent Extension; ADZYNMA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:32:46Z | 2025-23864 | 0 | 0 | 09000064b910a420 |
| FDA-2024-E-1293-0006 | FDA | FDA-2024-E-1293 | Determination of Regulatory Review Period for Purposes of Patent Extension; ZELSUVMI | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2026-02-28T10:00:12Z | 2025-23868 | 0 | 0 | 09000064b910a4a8 |
| FDA-2024-E-1287-0007 | FDA | FDA-2024-E-1287 | Determination of Regulatory Review Period for Purposes of Patent Extension; ADZYNMA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:37:21Z | 2025-23864 | 0 | 0 | 09000064b910aaad |
| FDA-2024-E-1286-0006 | FDA | FDA-2024-E-1286 | Determination of Regulatory Review Period for Purposes of Patent Extension; ADZYNMA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:35:54Z | 2025-23864 | 0 | 0 | 09000064b910aaac |
| FDA-2025-N-6971-0001 | FDA | FDA-2025-N-6971 | Authorization of Emergency Use for Two Animal Drugs for the Treatment of New World Screwworm; Availability | Notice | Announcement | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2025-12-29T20:06:23Z | 2025-23914 | 0 | 0 | 09000064b910a2c5 | |
| FDA-2024-E-3865-0007 | FDA | FDA-2024-E-3865 | Determination of Regulatory Review Period for Purposes of Patent Extension; OJEMDA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:57:00Z | 2025-23867 | 0 | 0 | 09000064b910a301 |
| FDA-2025-N-4684-0001 | FDA | FDA-2025-N-4684 | Egis Pharmaceuticals Limited, et.al.; Proposal To Withdraw Approval of Three Abbreviated New Drug Applications; Opportunity for a Hearing | Notice | Withdrawal | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:49:40Z | 2025-23870 | 0 | 0 | 09000064b910a3d3 |
| FDA-2025-N-3656-0002 | FDA | FDA-2025-N-3656 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practices for Positron Emission Tomography Drugs | Notice | 30 Day Proposed Information Collection | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-01-29T04:59:59Z | 2026-01-31T13:12:34Z | 2025-23859 | 0 | 0 | 09000064b910a46c |
| FDA-2025-P-5560-0023 | FDA | FDA-2025-P-5560 | Medical Devices; Exemption From Premarket Notification: Radiology Computer-Aided Detection and/or Diagnosis Devices and Computer-Aided Triage and Notification Devices | Notice | Announcement | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2026-02-28T10:00:12Z | 2025-23901 | 0 | 0 | 09000064b910a2ff |
| FDA-2024-E-1285-0007 | FDA | FDA-2024-E-1285 | Determination of Regulatory Review Period for Purposes of Patent Extension; ADZYNMA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:34:39Z | 2025-23864 | 0 | 0 | 09000064b91077dc |
| FDA-2024-E-1288-0007 | FDA | FDA-2024-E-1288 | Determination of Regulatory Review Period for Purposes of Patent Extension; ADZYNMA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:39:03Z | 2025-23864 | 0 | 0 | 09000064b910acd7 |
| FDA-2025-E-0917-0006 | FDA | FDA-2025-E-0917 | Determination of Regulatory Review Period for Purposes of Patent Extension; ALHEMO | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T20:38:53Z | 2025-23863 | 0 | 0 | 09000064b9106d07 |
| FDA-2025-N-6896-0001 | FDA | FDA-2025-N-6896 | Over-the-Counter Monograph Drug User Fee Amendments—OTC Monograph Order Request Fee Rates for Fiscal Year 2026 | Notice | Announcement | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2025-12-29T19:44:43Z | 2025-23852 | 0 | 0 | 09000064b910a41f | |
| FDA-2023-E-3236-0006 | FDA | FDA-2023-E-3236 | Determination of Regulatory Review Period for Purposes of Patent Extension; LEQEMBI | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T20:09:09Z | 2025-23865 | 0 | 0 | 09000064b910a288 |
| FDA-2025-E-0923-0006 | FDA | FDA-2025-E-0923 | Determination of Regulatory Review Period for Purposes of Patent Extension; ROMVIMZA | Notice | Determinations | 2025-12-29T05:00:00Z | 2025 | 12 | 2025-12-29T05:00:00Z | 2026-02-28T04:59:59Z | 2025-12-29T19:54:00Z | 2025-23862 | 0 | 0 | 09000064b910a397 |
| FDA-2025-N-1210-0002 | FDA | FDA-2025-N-1210 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Postmarket Surveillance of Medical Devices | Notice | 30 Day Proposed Information Collection | 2025-12-23T05:00:00Z | 2025 | 12 | 2025-12-23T05:00:00Z | 2026-01-22T04:59:59Z | 2026-01-24T13:18:31Z | 2025-23630 | 0 | 0 | 09000064b91065e6 |
| FDA-2023-D-2204-0005 | FDA | FDA-2023-D-2204 | Formal Dispute Resolution and Administrative Hearings of Final Administrative Orders Under Section 505G of the Federal Food, Drug, and Cosmetic Act; Guidance for Industry; Availability | Notice | Notice of Availability | 2025-12-23T05:00:00Z | 2025 | 12 | 2025-12-23T05:00:00Z | 2025-12-23T18:49:14Z | 2025-23707 | 0 | 0 | 09000064b91065e7 | |
| FWS-R4-ES-2025-1067-0001 | FWS | Receipt of Incidental Take Permit Application and Proposed Habitat Conservation Plan for the Sand Skink and Blue-tailed Mole Skink; Osceola County, FL; Categorical Exclusion (Westside Technology Park) FWS-R4-ES-2025-1067 | Receipt of Incidental Take Permit Application and Proposed Habitat Conservation Plan for the Sand Skink and Blue-Tailed Mole Skink; Osceola County, FL; Categorical Exclusion | Notice | 2025-12-23T05:00:00Z | 2025 | 12 | 2025-12-23T05:00:00Z | 2026-01-23T04:59:59Z | 2026-01-24T13:18:34Z | 2025-23647 | 0 | 0 | 09000064b9107ae1 | |
| FWS-HQ-IA-2025-0935-0001 | FWS | Agency Information Collection Activities; Federal Fish and Wildlife Permit Applications and Reports – Management Authority FWS-HQ-IA-2025-0935 | Agency Information Collection Activities; Federal Fish and Wildlife Permit Applications and Reports--Management Authority | Notice | 2025-12-23T05:00:00Z | 2025 | 12 | 2025-12-23T05:00:00Z | 2026-02-24T04:59:59Z | 2026-02-24T10:00:11Z | 2025-23694 | 0 | 0 | 09000064b9107a7e | |
| USDA_FRDOC_0001-3247 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Request for Information: Refined Sugar; Correction | Notice | 2025-12-22T05:00:00Z | 2025 | 12 | 2025-12-22T05:00:00Z | 2025-12-22T17:45:06Z | 2025-23604 | 0 | 0 | 09000064b90fd296 | ||
| USDA_FRDOC_0001-3248 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Agency Information Collection Activities; Proposals, Submissions, and Approvals | Notice | 2025-12-22T05:00:00Z | 2025 | 12 | 2025-12-22T05:00:00Z | 2025-12-22T17:45:35Z | 2025-23631 | 0 | 0 | 09000064b90fd3fd | ||
| EPA_FRDOC_0001-32449 | EPA | EPA_FRDOC_0001 | Environmental Impact Statements; Availability, etc. | Notice | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T17:16:18Z | 2025-23436 | 0 | 0 | 09000064b90f52ae | ||
| EPA-HQ-OPP-2025-0029-0003 | EPA | EPA-HQ-OPP-2025-0029 | Cancellation Order for Certain Pesticide Registrations and/or Amendments to Terminate Uses | Notice | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:21:35Z | 2025-23444 | 0 | 0 | 09000064b90f48af | ||
| FDA-2024-N-4731-0003 | FDA | FDA-2024-N-4731 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:08:09Z | 2025-23483 | 0 | 0 | 09000064b90f0496 | |
| FDA-2025-N-0383-0006 | FDA | FDA-2025-N-0383 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:14:36Z | 2025-23483 | 0 | 0 | 09000064b90f049b | |
| FDA-2025-N-6076-0001 | FDA | FDA-2025-N-6076 | Agency Information Collection Activities; Proposed Collection; Comment Request; Required Warnings for Cigarette Packages and Advertisements | Notice | 60 Day Proposed Information Collection | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2026-02-18T04:59:59Z | 2026-01-24T13:18:20Z | 2025-23474 | 0 | 0 | 09000064b90f519a |
| FDA-2024-N-5468-0010 | FDA | FDA-2024-N-5468 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:09:54Z | 2025-23483 | 0 | 0 | 09000064b90f0498 | |
| FDA-2025-P-1562-0004 | FDA | FDA-2025-P-1562 | Determination That DEXCHLORPHENIRAMINE MALEATE (Dexchlorpheniramine Maleate, Oral Syrup, 2 Milligrams/5 Milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T19:43:25Z | 2025-23419 | 0 | 0 | 09000064b90f5231 | |
| FDA-2025-N-0338-0004 | FDA | FDA-2025-N-0338 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:45:55Z | 2025-23483 | 0 | 0 | 09000064b90f5736 | |
| FDA-2025-N-0082-0009 | FDA | FDA-2025-N-0082 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:50:27Z | 2025-23483 | 0 | 0 | 09000064b90f573c | |
| FDA-2025-P-1304-0004 | FDA | FDA-2025-P-1304 | Determination That EFFEXOR XR (Venlafaxine Hydrochloride) Extended- Release Capsule, 100 Milligrams, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T21:21:26Z | 2025-23408 | 0 | 0 | 09000064b90f5195 | |
| FDA-2024-N-5603-0004 | FDA | FDA-2024-N-5603 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:06:25Z | 2025-23483 | 0 | 0 | 09000064b90f51e3 | |
| FDA-2024-N-5234-0003 | FDA | FDA-2024-N-5234 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:11:44Z | 2025-23483 | 0 | 0 | 09000064b90f0499 | |
| FDA-2025-N-0123-0006 | FDA | FDA-2025-N-0123 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:13:18Z | 2025-23483 | 0 | 0 | 09000064b90f049a | |
| FDA-2025-N-4683-0001 | FDA | FDA-2025-N-4683 | Issuance of Priority Review Voucher; Rare Pediatric Disease Product; FORZINITY (Elamipretide) | Notice | Announcement | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T19:35:42Z | 2025-23409 | 0 | 0 | 09000064b90f5277 | |
| FDA-2023-D-5021-0018 | FDA | FDA-2023-D-5021 | Processes and Practices Applicable to Bioresearch Monitoring Inspections; Guidance for Industry; Availability | Notice | Notice of Availability | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:54:43Z | 2025-23404 | 0 | 0 | 09000064b90f519d | |
| FDA-2025-N-0183-0005 | FDA | FDA-2025-N-0183 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:48:14Z | 2025-23483 | 0 | 0 | 09000064b90f573a | |
| FDA-2025-N-0349-0006 | FDA | FDA-2025-N-0349 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:49:25Z | 2025-23483 | 0 | 0 | 09000064b90f573b | |
| FDA-2025-N-4682-0001 | FDA | FDA-2025-N-4682 | Notice of Approval of Product Under Voucher: Rare Pediatric Disease Priority Review Voucher; KEYTRUDA QLEX (pembrolizumab and berahyaluronidase alfa-pmph) | Notice | Notice of Approval | 2025-12-19T05:00:00Z | 2025 | 12 | 2025-12-19T05:00:00Z | 2025-12-19T20:02:51Z | 2025-23410 | 0 | 0 | 09000064b90f51e4 | |
| EPA-HQ-OAR-2022-0070-0005 | EPA | NSPS for Flexible Vinyl and Urethane Coating and Printing (40 CFR Part 60, Subpart FFF) (Renewal) EPA-HQ-OAR-2022-0070 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: New Source Performance Standards for Flexible Vinyl and Urethane Coating and Printing | Notice | Information Collection Request (ICR) | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T05:00:00Z | 2026-01-21T04:59:59Z | 2025-12-18T18:55:30Z | 2025-23271 | 0 | 0 | 09000064b90ee7f8 |
| EPA-HQ-OAR-2022-0021-0005 | EPA | NESHAP for Secondary Aluminum Production (40 CFR Part 63, Subpart RRR) (Renewal) EPA-HQ-OAR-2022-0021 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: National Emission Standards for Hazardous Air Pollutants for Secondary Aluminum Production | Notice | Information Collection Request (ICR) | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T05:00:00Z | 2026-01-21T04:59:59Z | 2025-12-18T18:50:33Z | 2025-23286 | 0 | 0 | 09000064b90ee844 |
| EPA-HQ-OW-2002-0070-0003 | EPA | EPA-HQ-OW-2002-0070 | Federal Register of September 27, 2001 [66 FR 49381] [FRL-7068-4] | Notice | Request for Comments | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T05:00:00Z | 2002-01-12T04:59:59Z | 2025-12-19T10:00:17Z | 01–24193 | 0 | 0 | 09000064b90f373c |
| FDA-2023-D-4395-0033 | FDA | FDA-2023-D-4395 | Use of Real-World Evidence To Support Regulatory Decision-Making for Medical Devices; Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T18:40:06Z | 2025-23252 | 0 | 0 | 09000064b90ee7f9 | ||
| FDA-2025-D-2246-0001 | FDA | FDA-2025-D-2246 | Questions and Answers Regarding Mandatory Cosmetics Recalls: Draft Guidance for Industry; Availability | Notice | Notice of Availability | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T18:30:54Z | 2025-23249 | 0 | 0 | 09000064b90eed0c | ||
| USDA_FRDOC_0001-3246 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Performance Review Board Members | Notice | 2025-12-18T05:00:00Z | 2025 | 12 | 2025-12-18T05:00:00Z | 2025-12-18T17:24:41Z | 2025-23255 | 0 | 0 | 09000064b90ee7fd | ||
| USDA_FRDOC_0001-3245 | USDA | Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 | Agency Information Collection Activities; Proposals, Submissions, and Approvals | Notice | 2025-12-17T05:00:00Z | 2025 | 12 | 2025-12-17T05:00:00Z | 2025-12-17T17:21:33Z | 2025-23114 | 0 | 0 | 09000064b90ea99e | ||
| EPA-HQ-OPP-2025-0026-0010 | EPA | EPA-HQ-OPP-2025-0026 | Pesticide Product Registration: Applications for New Uses October 2025 | Notice | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2026-01-16T04:59:59Z | 2025-12-17T10:00:30Z | 2025-22932 | 0 | 0 | 09000064b90da716 | |
| EPA-HQ-OPP-2025-2400-0001 | EPA | EPA-HQ-OPP-2025-2400 | Pesticide Product Registration: Applications for New Active Ingredients October 2025 | Notice | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2026-01-16T04:59:59Z | 2026-01-17T13:21:35Z | 2025-22935 | 0 | 0 | 09000064b90d382a | |
| EPA-HQ-OPP-2025-0024-0004 | EPA | EPA-HQ-OPP-2025-0024 | Pesticide Product Registration: Applications for New Active Ingredients October 2025 | Notice | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2025-12-17T02:18:41Z | 2025-22935 | 0 | 0 | 09000064b90da748 | ||
| EPA-HQ-OPP-2025-2566-0001 | EPA | EPA-HQ-OPP-2025-2566 | Pesticide Product Registration: Applications for New Active Ingredients October 2025 | Notice | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2026-01-16T04:59:59Z | 2025-12-16T21:37:49Z | 2025-22935 | 0 | 0 | 09000064b90d3829 | |
| EPA-HQ-OPP-2025-2565-0001 | EPA | EPA-HQ-OPP-2025-2565 | Pesticide Product Registration: Applications for New Uses October 2025 | Notice | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2026-01-16T04:59:59Z | 2025-12-16T19:22:53Z | 2025-22932 | 0 | 0 | 09000064b90dc7cc | |
| FDA-2021-D-0368-0012 | FDA | FDA-2021-D-0368 | Investigator Responsibilities—Safety Reporting for Investigational Drugs and Devices; Guidance for Investigators, Industry, and Institutional Review Boards; Availability | Notice | Notice of Availability | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2025-12-16T18:17:17Z | 2025-22869 | 0 | 0 | 09000064b90da8c2 | |
| FDA-2020-D-2099-0012 | FDA | FDA-2020-D-2099 | Sponsor Responsibilities—Safety Reporting Requirements and Safety Assessment for Investigational New Drug Application and Bioavailability/ Bioequivalence Studies; Guidance for Industry; Availability | Notice | Notice of Availability | 2025-12-16T05:00:00Z | 2025 | 12 | 2025-12-16T05:00:00Z | 2025-12-16T18:44:45Z | 2025-22870 | 0 | 0 | 09000064b90da7e0 | |
| EPA-HQ-OPP-2017-0720-0064 | EPA | EPA-HQ-OPP-2017-0720 | Pesticide Registration Review: Draft Human Health and/or Ecological Risk Assessment for Metrafenone | Notice | 2025-12-15T05:00:00Z | 2025 | 12 | 2025-12-15T21:41:54Z | 2025-22811 | 0 | 0 | 09000064b90d32d3 | |||
| EPA-HQ-OPP-2020-0032-0019 | EPA | EPA-HQ-OPP-2020-0032 | Pesticide Registration Review: Draft Human Health and/or Ecological Risk Assessment for Metrafenone | Notice | 2025-12-15T05:00:00Z | 2025 | 12 | 2025-12-15T05:00:00Z | 2026-02-14T04:59:59Z | 2026-02-14T13:16:56Z | 2025-22811 | 0 | 0 | 09000064b90d0baa | |
| EPA-HQ-OPP-2021-0749-0015 | EPA | EPA-HQ-OPP-2021-0749 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Foreign Purchaser Acknowledgement Statement of Unregistered Pesticides | Notice | 2025-12-15T05:00:00Z | 2025 | 12 | 2025-12-15T05:00:00Z | 2026-02-24T04:59:59Z | 2026-02-06T00:48:03Z | 2025-22741 | 0 | 0 | 09000064b90d33db | |
| FWS-HQ-ES-2025-0613-0001 | FWS | Agency Information Collection Activities; Approval Procedures for Incidental Harassment Authorizations of Marine Mammals FWS-HQ-ES-2025-0613 | Agency Information Collection Activities; Approval Procedures for Incidental Harassment Authorizations of Marine Mammals | Notice | 2025-12-15T05:00:00Z | 2025 | 12 | 2025-12-15T05:00:00Z | 2026-02-14T04:59:59Z | 2026-02-14T13:16:56Z | 2025-22770 | 0 | 0 | 09000064b90d0b21 | |
| EPA-HQ-OPP-2025-0049-0012 | EPA | EPA-HQ-OPP-2025-0049 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Bilingual Pesticide Labeling Tracking | Notice | Information Collection Request (ICR) | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2026-01-13T04:59:59Z | 2026-01-17T13:21:29Z | 2025-22589 | 0 | 0 | 09000064b90c85ae |
| EPA_FRDOC_0001-32433 | EPA | EPA_FRDOC_0001 | Environmental Impact Statements; Availability, etc. | Notice | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T17:24:03Z | 2025-22652 | 0 | 0 | 09000064b90c8692 | ||
| FDA-2024-P-2952-0006 | FDA | FDA-2024-P-2952 | Determination That LUNELLE (Estradiol Cypionate and Medroxyprogesterone Acetate) Injectable, 5 Milligrams/0.5 Milliliter and 25 Milligrams/0.5 Milliliter, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T22:12:49Z | 2025-22680 | 0 | 0 | 09000064b90cb51b | |
| FDA-2025-N-6494-0001 | FDA | FDA-2025-N-6494 | Amending Over-the-Counter Monograph M020: Sunscreen Drug Products for Over-the-Counter Human Use | Notice | Notice of Availability | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2026-01-27T04:59:59Z | 2026-01-31T13:11:51Z | 2025-22649 | 0 | 0 | 09000064b90c85ec |
| FDA-2025-N-6077-0001 | FDA | FDA-2025-N-6077 | Pfizer Inc., U.S. Agent for King Pharmaceuticals LLC, et al.; Withdrawal of Approval of 20 Abbreviated New Drug Applications | Notice | Withdrawal | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T19:37:48Z | 2025-22683 | 0 | 0 | 09000064b90c8624 | |
| FDA-2020-P-1617-0005 | FDA | FDA-2020-P-1617 | Determination That BACTROBAN (Mupirocin) Nasal Ointment, 2%, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T19:43:45Z | 2025-22682 | 0 | 0 | 09000064b90c85b0 | |
| FDA-2025-N-4732-0001 | FDA | FDA-2025-N-4732 | Determination That ZANTAC (Ranitidine Hydrochloride) Injection, Equivalent to 25 Milligrams Base/ Milliliter, Has Not Been Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T19:55:43Z | 2025-22676 | 0 | 0 | 09000064b90c85aa | |
| FDA-2025-N-4734-0001 | FDA | FDA-2025-N-4734 | Determination That DEMEROL (Meperidine Hydrochloride) Tablet, 100 Milligrams, and Other Drug Products Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness | Notice | Determinations | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-12T19:21:36Z | 2025-22681 | 0 | 0 | 09000064b90c8657 | |
| FDA-2025-N-5997-0001 | FDA | FDA-2025-N-5997 | Biosimilar User Fee Act; Stakeholder Consultation Meetings on Biosimilar User Fee Act Reauthorization; Request for Notification of Stakeholder Intention To Participate | Notice | General Notice | 2025-12-12T05:00:00Z | 2025 | 12 | 2025-12-12T05:00:00Z | 2025-12-13T00:47:14Z | 2025-22619 | 0 | 0 | 09000064b90c85ad | |
| EPA_FRDOC_0001-32426 | EPA | EPA_FRDOC_0001 | Performance Review Board Members | Notice | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2025-12-11T17:19:07Z | 2025-22520 | 0 | 0 | 09000064b90c5580 | ||
| EPA_FRDOC_0001-32421 | EPA | EPA_FRDOC_0001 | Charter Amendments, Establishments, Renewals and Terminations: Farm, Ranch, and Rural Communities Advisory Committee | Notice | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2025-12-11T17:18:55Z | 2025-22561 | 0 | 0 | 09000064b90c30e6 | ||
| EPA-HQ-OPP-2017-0720-0063 | EPA | EPA-HQ-OPP-2017-0720 | Pesticide Registration Review: Pesticide Dockets Opened for Review and Comment | Notice | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-12T02:43:13Z | 2025-22514 | 0 | 0 | 09000064b90c5532 | |||
| EPA-HQ-OPP-2025-0018-0001 | EPA | EPA-HQ-OPP-2025-0018 | Pesticide Registration Review: Pesticide Dockets Opened for Review and Comment | Notice | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-14T13:16:44Z | 2025-22514 | 0 | 0 | 09000064b90c1dff | |
| EPA-HQ-OLEM-2018-0102-0011 | EPA | RCRA Expanded Pubic Participation EPA-HQ-OLEM-2018-0102 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: RCRA Expanded Public Participation | Notice | Information Collection Request (ICR) | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2025-12-11T18:26:32Z | 2025-22528 | 0 | 0 | 09000064b90c560e |
| EPA-HQ-SFUND-2006-0361-0031 | EPA | EPA-HQ-SFUND-2006-0361 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Trade Secret Claims for Community Right-to-Know and Emergency Planning (Renewal) | Notice | Information Collection Request (ICR) | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2026-01-31T13:11:45Z | 2025-22527 | 0 | 0 | 09000064b90c3069 |
| EPA-HQ-OLEM-2018-0013-0013 | EPA | Revisions to the RCRA Definition of Solid Waste EPA-HQ-OLEM-2018-0013 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Revisions to the RCRA Definition of Solid Waste | Notice | Information Collection Request (ICR) | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-14T13:16:49Z | 2025-22529 | 0 | 0 | 09000064b90c557d |
| EPA-HQ-OPP-2024-0218-0001 | EPA | EPA-HQ-OPP-2024-0218 | Pesticide Registration Review: Pesticide Dockets Opened for Review and Comment | Notice | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2025-12-12T03:38:05Z | 0 | 0 | 09000064b90c757a | ||
| FDA-2025-N-6743-0001 | FDA | FDA-2025-N-6743 | Food and Drug Administration Expert Panel on Testosterone Replacement Therapy for Men; Request for Information | Notice | Requests for Information (RFI) | 2025-12-11T05:00:00Z | 2025 | 12 | 2025-12-11T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-20T20:29:54Z | 2025-22466 | 0 | 0 | 09000064b90c309f |
| FDA-2024-E-1291-0006 | FDA | FDA-2024-E-1291 | Determination of Regulatory Review Period for Purposes of Patent Extension; FILSUVEZ | Notice | Determinations | 2025-12-10T05:00:00Z | 2025 | 12 | 2025-12-10T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-07T13:13:03Z | 2025-22380 | 0 | 0 | 09000064b90c192e |
| FDA-2024-E-1292-0006 | FDA | FDA-2024-E-1292 | Determination of Regulatory Review Period for Purposes of Patent Extension; FILSUVEZ | Notice | Determinations | 2025-12-10T05:00:00Z | 2025 | 12 | 2025-12-10T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-07T13:13:03Z | 2025-22380 | 0 | 0 | 09000064b90c192f |
| FDA-2024-E-1290-0006 | FDA | FDA-2024-E-1290 | Determination of Regulatory Review Period for Purposes of Patent Extension; FILSUVEZ | Notice | Determinations | 2025-12-10T05:00:00Z | 2025 | 12 | 2025-12-10T05:00:00Z | 2026-02-10T04:59:59Z | 2026-02-07T13:13:03Z | 2025-22380 | 0 | 0 | 09000064b90c167a |
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CREATE TABLE documents (
id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
subtype TEXT,
posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);