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Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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

comment_end_date
A FULL UTC INSTANT, not a calendar date, despite the column name: '2026-08-29T03:59:59Z' is 11:59:59 PM EASTERN on 2026-08-28. Federal comment periods close at 11:59:59 PM Eastern, so the UTC calendar date is ONE DAY LATER than the official deadline on every end-of-day close — 444,689 of the 444,690 populated rows (measured 2026-09-06). Convert to America/New_York before presenting a deadline, and compare with julianday(comment_end_date) > julianday('now'): a plain > datetime('now') is a TEXT comparison between two different formats and keeps already-closed dockets matching for up to ~20 hours. The sibling column on open_comments.documents WAS corrected to an Eastern calendar date (queue #498); this one is unchanged and still an instant — the two databases do not agree on grain. (queue #644)
comment_start_date
A FULL UTC INSTANT, not a calendar date, despite the column name — same grain as comment_end_date on this table. Convert to America/New_York before presenting it. (queue #644)

316,840 rows where document_type = "Notice" sorted by posted_date descending

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posted_year >30

  • 2006 17,528
  • 2024 16,166
  • 2013 15,687
  • 2014 15,686
  • 2016 15,200
  • 2015 14,834
  • 2020 14,734
  • 2012 14,704
  • 2017 14,666
  • 2022 14,502
  • 2021 14,438
  • 2018 14,416
  • 2011 14,203
  • 2019 14,203
  • 2023 14,007
  • 2007 13,791
  • 2010 13,720
  • 2009 12,427
  • 2025 12,121
  • 2008 11,709
  • 2005 7,212
  • 2026 3,696
  • 2004 3,238
  • 2003 3,177
  • 2002 2,450
  • 2001 1,626
  • 2000 1,570
  • 1999 1,266
  • 1998 1,215
  • 1996 1,065
  • …

agency_id >30

  • SEC 40,880
  • FERC 36,639
  • EPA 22,691
  • FDA 20,143
  • NIH 13,111
  • ITA 13,105
  • FMCSA 12,886
  • DOT 11,536
  • NRC 9,599
  • FAA 8,662
  • FEMA 7,753
  • HUD 6,287
  • VA 6,126
  • FCC 6,017
  • CMS 5,041
  • USPS 4,633
  • DOE 4,487
  • DOD 3,782
  • NSF 3,705
  • STB 3,679
  • ED 3,511
  • USDA 3,350
  • FS 3,119
  • USCG 2,954
  • OSHA 2,918
  • MARAD 2,860
  • DOL 2,452
  • FRA 2,447
  • FMC 2,399
  • CDC 2,224
  • …

document_type 1

  • Notice · 316,840 ✖
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-2026-N-0004-0002 FDA Notice of Availability when we issue Emergency Use Authorizations (EUAs) for New World Screwworm FDA-2026-N-0004 Authorization of Emergency Use for Four Animal Drugs for the Prevention and Treatment of New World Screwworm; Availability Notice Notice of Availability 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T17:36:31Z 2026-21084 0 0 09000064b967171d
FDA-2026-N-1832-0079 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1344 - Part 1 of 2 - L-theanine (chemically synthesized) Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:36:14Z   0 0 09000064b966c808
FDA-2026-N-1832-0074 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1339 - L-ergothioneine produced by Escherichia coli EG38, expressing enzymes from Mycolicibacterium smegmatis, Schizophyllum commune H4-8, and Claviceps purpurea Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:17Z   0 0 09000064b966cc7d
FDA-2026-N-1832-0075 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1340 - L-ergothioneine produced by Escherichia coli K12 MG1655, expressing enzymes from Mycolicibacterium smegmatis, Methylobacterium pseudosasicola, Microcoleus sp. PCC 7713, and Neurospora crassa Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:21Z   0 0 09000064b966cc7e
FDA-2026-N-1832-0087 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1350 - Part 2 of 2 - Rebaudioside M produced by enzymatic treatment of rebaudioside A purified from the leaves of Stevia rebaudiana (Bertoni) Bertoni Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:38:34Z   0 0 09000064b966cc86
FDA-2026-N-1832-0072 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1337 - Heat-killed Lacticaseibacillus paracasei 327 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:01Z   0 0 09000064b966cc7b
FDA-2026-N-1832-0078 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1343 - L-ergothioneine produced by Escherichia coli CGMCC 24897, expressing enzymes from Trichoderma reesei ATCC 13631 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:55Z   0 0 09000064b966cc81
FDA-2026-N-1832-0080 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1344 - Part 2 of 2 - L-theanine (chemically synthesized) Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:36:19Z   0 0 09000064b966ecd9
FDA-2026-N-1832-0076 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1341 - Alternansucrase enzyme preparation produced by Escherichia coli expressing a gene encoding an alternansucrase enzyme from Leuconostoc mesenteroides Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:39Z   0 0 09000064b966cc7f
FDA-2026-N-1832-0077 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1342 - D-psicose Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:51Z   0 0 09000064b966cc80
FDA-2026-N-1832-0085 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1349 - Polysorbate 65 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:38:20Z   0 0 09000064b966cc84
FDA-2026-N-1832-0092 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1355 - Rebaudioside M9 produced by enzymatic treatment of rebaudioside A purified from the leaves of Stevia rebaudiana (Bertoni) Bertoni Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:39:12Z   0 0 09000064b966cc8a
FDA-2026-N-1832-0081 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1345 - Bacillus subtilis NCIMB 30283 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:36:49Z   0 0 09000064b966ecda
FDA-2026-N-1832-0090 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1353 - L-ergothioneine produced by Escherichia coli strain ERG2201 expressing genes encoding enzymes from Methylobacterium aquaticum, Trichoderma reesei, and Mycolicibacterium smegmatis Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:39:04Z   0 0 09000064b966ecde
FDA-2026-N-1832-0094 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1358 - Lacticaseibacillus paracasei subsp. paracasei GDMCC 60960 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:40:24Z   0 0 09000064b966ece0
FDA-2026-N-1832-0091 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1354 - Rebaudioside M produced by enzymatic treatment of rebaudioside A purified from the leaves of Stevia rebaudiana (Bertoni) Bertoni Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:39:08Z   0 0 09000064b966cc89
FDA-2026-N-1832-0082 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1346 - Saccharomyces pastorianus “BY-1198” expressing a gene encoding an α-acetolactate decarboxylase enzyme from Acetobacter aceti Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:37:29Z   0 0 09000064b966ecdb
FDA-2026-N-1832-0093 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1357 - Yeast protein produced by a non-genetically engineered Saccharomyces cerevisiae strain Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:40:20Z   0 0 09000064b966ecdf
FDA-2026-N-1832-0084 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1348 - β-casein protein preparation Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:37:52Z   0 0 09000064b966cc83
FDA-2026-N-1832-0086 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1350 - Part 1 of 2 - Rebaudioside M produced by enzymatic treatment of rebaudioside A purified from the leaves of Stevia rebaudiana (Bertoni) Bertoni Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:38:29Z   0 0 09000064b966cc85
FDA-2026-N-1832-0089 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1352 - 6-phytase enzyme preparation produced by Trichoderma reesei expressing a gene encoding 6-phytase from Escherichia coli Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:38:55Z   0 0 09000064b966ecdc
FDA-2026-N-11624-0001 FDA Request for Nominations for Voting Members on a Public Advisory Committee; Tobacco Products Scientific Advisory Committee FDA-2026-N-11624 Request for Nominations for Voting Members on a Public Advisory Committee; Tobacco Products Scientific Advisory Committee (TPSAC) Notice Request for Nominations 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T16:58:08Z 2026-21027 0 0 09000064b9671769
FDA-2026-N-1832-0073 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1338 - Brazzein preparation produced by a genetically engineered strain of Komagataella phaffii “BG12” expressing a gene encoding for brazzein from Pentadiplandra brazzeana Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:35:05Z   0 0 09000064b966cc7c
FDA-2026-N-1832-0083 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1347 - Lactobacillus plantarum KCTC 13101BP Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:37:49Z   0 0 09000064b966cc82
FDA-2026-N-1832-0088 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1351 - Heat-killed biomass of Xanthobacter sp. DSM 34079 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:38:48Z   0 0 09000064b966cc87
FDA-2026-N-1832-0095 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2026 FDA-2026-N-1832 GRAS Notice (GRN) 1359 - Bifidobacterium animalis subsp. lactis CCTCC M 2013336 Notice General Notice 2026-10-15T04:00:00Z 2026 10 2026-10-15T04:00:00Z   2026-10-15T19:40:33Z   0 0 09000064b966ece1
APHIS-2026-0001-0007 APHIS Ball Horticultural Company: Availability of a Petition for a Determination of Nonregulated Status and Draft Plant Pest Risk Assessment for Red Flower Petal African marigold (Tagetes erecta) Event pBALL123-022-BE113. APHIS-2026-0001 Determination of Nonregulated Status: Ball Horticultural Co.; Red Flower Petals African marigold (Tagetes erecta) Event pBALL123-022-BE113 3 Notice Determinations 2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z   2026-10-14T16:56:41Z 2026-20961 0 0 09000064b966afff
FDA-2026-N-0008-0017 FDA Advisory Committee FDA-2026-N-0008 Advisory Committee; Cellular, Tissue, and Gene Therapies Advisory Committee; Renewal Notice Notice of Renewal 2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z   2026-10-14T18:23:42Z 2026-20989 0 0 09000064b966b003
FDA-2026-N-7131-0008 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Infant Formula Requirements FDA-2026-N-7131 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Infant Formula Requirements Notice 30 Day Proposed Information Collection 2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z 2026-11-14T04:59:59Z 2026-10-14T18:28:35Z 2026-20980 1 0 09000064b966affd
FDA-2026-N-6739-0004 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Cosmetic Labeling Requirements and Facility Registration and Cosmetic Product Listing Program FDA-2026-N-6739 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Requirements for Cosmetic Products Notice 30 Day Proposed Information Collection 2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z 2026-11-14T04:59:59Z 2026-10-14T18:20:53Z 2026-20990 1 0 09000064b966b085
FDA-2026-N-7338-0003 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Voluntary National Retail Food Regulatory Program Standards FDA-2026-N-7338 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Voluntary National Retail Food Regulatory Program Standards Notice 30 Day Proposed Information Collection 2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z 2026-11-14T04:59:59Z 2026-10-14T19:15:47Z 2026-20981 1 0 09000064b966aeb3
USDA_FRDOC_0001-3378 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-14T04:00:00Z 2026 10 2026-10-14T04:00:00Z   2026-10-14T16:53:15Z 2026-20985 0 0 09000064b965c83e
FDA-2024-D-2581-0010 FDA Postapproval Manufacturing Changes to Biosimilar and Interchangeable Biosimilar Products: Questions and Answers; Draft Guidance for Industry; Availability FDA-2024-D-2581 Postapproval Manufacturing Changes to Biosimilar and Interchangeable Biosimilar Products: Questions and Answers; Guidance for Industry; Availability Notice Notice of Availability 2026-10-13T04:00:00Z 2026 10 2026-10-13T04:00:00Z   2026-10-13T20:18:36Z 2026-20817 0 0 09000064b965c59f
EPA_FRDOC_0001-33209 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Environmental Impact Statements; Availability, etc. Notice   2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T16:26:04Z 2026-20738 0 0 09000064b9657796
FDA-2026-N-10835-0001 FDA Par Health USA LLC, U.S. Agent for PH Health Limited et al.; Withdrawal of Approval of 37 Abbreviated New Drug Applications FDA-2026-N-10835 Par Health USA LLC, U.S. Agent for PH Health Limited, et al.; Withdrawal of Approval of 37 Abbreviated New Drug Applications Notice Withdrawal 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T18:48:57Z 2026-20762 0 0 09000064b96576b4
FDA-2026-N-7426-0003 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Expanded Access to Investigational Drugs for Treatment Use FDA-2026-N-7426 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Expanded Access to Investigational Drugs for Treatment Use Notice 30 Day Proposed Information Collection 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z 2026-11-10T04:59:59Z 2026-10-09T18:12:21Z 2026-20765 1 0 09000064b96577e0
FDA-2014-N-0053-1398 FDA Designation of High-Risk Foods for Tracing; Request for Comments and for Scientific Data and Information FDA-2014-N-0053 Challenges and Solutions in Lot-Level Food Traceability; Public Meeting Notice Public Meetings 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z 2026-12-07T04:59:59Z 2026-10-09T18:53:04Z 2026-20720 1 0 09000064b9653e73
FDA-2026-N-10786-0001 FDA Issuance of Priority Review Voucher; Rare Pediatric Disease Product; ZANVASTRO (zilganersen) FDA-2026-N-10786 Issuance of Priority Review Voucher; Rare Pediatric Disease Product; ZANVASTRO (Zilganersen) Notice Announcement 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T18:42:00Z 2026-20769 0 0 09000064b9657707
FDA-2026-N-5816-0002 FDA Elite Laboratories, Inc. et al.; Withdrawal of Approval of 16 Abbreviated New Drug Applications FDA-2026-N-5816 Elite Laboratories, Inc. et al.; Withdrawal of Approval of 16 Abbreviated New Drug Applications; Correction Notice Correction 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T18:36:17Z 2026-20730 0 0 09000064b965774f
FDA-2020-E-1882-0005 FDA Patent Term Extension Application for MONOFERRIC (ferric derisomaltose), Patent No. 8,815,301 FDA-2020-E-1882 Determination of Regulatory Review Period for Purposes of Patent Extension; MONOFERRIC Notice Determinations 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z 2026-12-09T04:59:59Z 2026-10-09T18:22:03Z 2026-20766 1 0 09000064b9657798
FDA-2026-N-10396-0001 FDA Amneal Pharmaceuticals of New York, LLC; Withdrawal of Approval of Abbreviated New Drug Application for Celecoxib Capsules, 50 Milligrams, 100 Milligrams, 200 Milligrams, and 400 Milligrams FDA-2026-N-10396 Amneal Pharmaceuticals of New York, LLC; Withdrawal of Approval of Abbreviated New Drug Application for Celecoxib Capsules, 50 Milligrams, 100 Milligrams, 200 Milligrams, and 400 Milligrams Notice Withdrawal 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T18:15:50Z 2026-20758 0 0 09000064b965779c
FDA-2026-P-4567-0004 FDA Requests that the FDA determine whether the Reference Listed Drug (RLD) LASIX ORAL SOLUTION, 10 mg/mL; New Drug Application (NDA) 017688 of SANOFI AVENTIS US LLC has been voluntarily withdrawn from sale for safety or efficacy reasons. FDA-2026-P-4567 Determination That LASIX (Furosemide) Oral Solution, 10 Milligrams/Milliliter, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice Determinations 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z   2026-10-09T17:53:11Z 2026-20764 0 0 09000064b96577e3
FDA-2026-N-6667-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Biologics License Applications (BLAs) FDA-2026-N-6667 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Biologics License Applications, Procedures and Requirements Notice 30 Day Proposed Information Collection 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z 2026-11-10T04:59:59Z 2026-10-10T09:00:59Z 2026-20768 1 0 09000064b9657794
FDA-2020-E-1892-0005 FDA Patent Term Extension Application for MONOFERRIC (ferric derisomaltose), Patent No. 10,414,831 FDA-2020-E-1892 Determination of Regulatory Review Period for Purposes of Patent Extension; MONOFERRIC Notice Determinations 2026-10-09T04:00:00Z 2026 10 2026-10-09T04:00:00Z 2026-12-09T04:59:59Z 2026-10-09T18:23:55Z 2026-20766 1 0 09000064b965705e
APHIS-2021-0081-0042 APHIS Chrysanthemum white rust APHIS-2021-0081 Imports: Chrysanthemum spp. Cuttings, and In Vitro Plantlets, and Synonymous Taxa; Decision to Deregulate Chrysanthemum White Rust Notice Availability of Environmental Assessment 2026-10-08T04:00:00Z 2026 10 2026-10-08T04:00:00Z   2026-10-08T16:32:26Z 2026-20631 0 0 09000064b9651f15
EPA-HQ-OPP-2025-0027-0004 EPA Transfer of Data EPA-HQ-OPP-2025-0027 Access to Confidential Business Information: Eastern Research Group Notice   2026-10-08T04:00:00Z 2026 10 2026-10-08T04:00:00Z   2026-10-08T20:22:47Z 2026-20639 0 0 09000064b9651d41
EPA_FRDOC_0001-33206 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Hearings, Meetings, Proceedings, etc.: Clean Air Scientific Advisory Committee on Oxides of Nitrogen Notice   2026-10-08T04:00:00Z 2026 10 2026-10-08T04:00:00Z   2026-10-08T16:26:15Z 2026-20608 0 0 09000064b9651e93
FDA-2026-N-7129-0005 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Event Program for Medical Devices: (Medical Product Safety Network (MedSun)) FDA-2026-N-7129 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Event Program for Medical Devices: (Medical Product Safety Network (MedSun)) Notice 30 Day Proposed Information Collection 2026-10-08T04:00:00Z 2026 10 2026-10-08T04:00:00Z 2026-11-10T04:59:59Z 2026-10-08T17:19:42Z 2026-20661 1 0 09000064b9651f14
FDA-2026-N-10605-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Channels of Trade Policy for Commodities With Residues of Pesticide Chemicals, for Which Tolerances Have Been Revoked, Suspended, or Modified by the Environmental Protection Agency Pursuant to Dietary Risk Considerations FDA-2026-N-10605 Agency Information Collection Activities; Proposed Collection; Comment Request; Channels of Trade Policy for Commodities With Residues of Pesticide Chemicals, for Which Tolerances Have Been Revoked, Suspended, or Modified by the Environmental Protection Agency Pursuant to Dietary Risk Considerations Notice 60 Day Proposed Information Collection 2026-10-08T04:00:00Z 2026 10 2026-10-08T04:00:00Z 2026-12-08T04:59:59Z 2026-10-08T17:22:43Z 2026-20663 1 0 09000064b9651d3d
FDA-2022-P-0558-0005 FDA Requests that the FDA to determine if the Reference Listed Drug (RLD), OXANDRIN (oxandrolone tablets, USP) 2.5 mg and 10 mg, NDA 013718 owned by Gemini Laboratories LLC was voluntarily withdrawn from sale for reasons of safety or effectiveness to facilitate the approval of generic version. FDA-2022-P-0558 Determination That Oxandrin (Oxandrolone) Tablets, 2.5 Milligrams and 10 Milligrams, Were Withdrawn From Sale for Reasons of Safety or Effectiveness; Correction Notice Correction 2026-10-07T04:00:00Z 2026 10 2026-10-07T04:00:00Z   2026-10-07T18:02:12Z 2026-20503 0 0 09000064b96482e9
FWS-HQ-OC-2026-4027-0001 FWS Hunting and Shooting Sports Conservation and Access Council; Request for Nominations FWS-HQ-OC-2026-4027 Hunting and Shooting Sports Conservation and Access Council; Request for Nominations Notice   2026-10-07T04:00:00Z 2026 10 2026-10-07T04:00:00Z   2026-10-07T16:48:22Z 2026-20555 0 0 09000064b9643567
FWS-R7-ES-2026-4357-0001 FWS Marine Mammals; Proposed Incidental Harassment Authorization for the Southern Beaufort Sea Stock of Polar Bears During Exploration Activities in the Arctic National Wildlife Refuge 1002 Area Alaska; Draft Environmental Assessment FWS-R7-ES-2026-4357 Hunting and Shooting Sports Conservation and Access Council; Request for Nominations Notice   2026-10-07T04:00:00Z 2026 10     2026-10-07T16:03:00Z   0 1 09000064b9643561
EPA-HQ-OPPT-2026-1849-0016 EPA Certain New Chemicals or Significant New Uses; Statements of Findings for 2026 EPA-HQ-OPPT-2026-1849 Certain New Chemicals or Significant New Uses: Statements of Findings—June 2026 Notice   2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T17:36:31Z 2026-20436 0 0 09000064b962e6ee
EPA-HQ-OAR-2021-0669-0009 EPA Yearly hydrofluorocarbon production and consumption allowances under the American Innovation and Manufacturing Act EPA-HQ-OAR-2021-0669 2027 Allowance Allocations for Production and Consumption of Regulated Substances under the American Innovation and Manufacturing Act, and Final Actions Establishing Administrative Consequences: Phasedown of Hydrofluorocarbons Notice   2026-10-06T04:00:00Z 2026 10     2026-10-06T17:14:30Z 2026-20389 0 0 09000064b962e77d
FDA-2026-N-11259-0001 FDA Issuance of Priority Review Voucher; Rare Pediatric Disease Product; FAYUVI (rebisufligene etisparvovec-hopf) FDA-2026-N-11259 Issuance of Priority Review Voucher; Rare Pediatric Disease Product; FAYUVI (rebisufligene etisparvovechopf) Notice Announcement 2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T18:28:00Z 2026-20434 0 0 09000064b962e73a
FDA-2026-P-3632-0007 FDA Requests that the FDA to determine that PRALIDOXIME CHLORIDE (AUTOINJECTOR) 600 mg/2 mL intramuscular solution, (NDA 018986) from Meridian Medical Technologies Inc. was not discontinued or withdrawn due to safety or efficacy reasons. FDA-2026-P-3632 Determination PRALIDOXIME CHLORIDE (Autoinjector) (Pralidoxime Chloride) Solution, 600 Milligrams/2 Milliliters (300 Milligrams/Milliliter), Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice Determinations 2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T18:37:10Z 2026-20442 0 0 09000064b962e6a8
FDA-2026-N-4291-0002 FDA Teva Pharmaceuticals USA, Inc., et al.; Withdrawal of Approval of 15 Abbreviated New Drug Applications FDA-2026-N-4291 Teva Pharmaceuticals USA, Inc., et al.; Withdrawal of Approval of 15 Abbreviated New Drug Applications; Correction Notice Correction 2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T18:38:22Z 2026-20460 0 0 09000064b962e6a7
FDA-2026-N-10429-0001 FDA Design and Safety Considerations for Clinical Trials Involving Ibogaine Drug Products; Request for Information FDA-2026-N-10429 Design and Safety Considerations for Clinical Trials Involving Ibogaine Drug Products; Request for Information Notice Requests for Information (RFI) 2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z 2026-11-21T04:59:59Z 2026-10-15T09:00:40Z 2026-20427 1 0 09000064b962e7b9
USDA_FRDOC_0001-3377 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T17:03:20Z 2026-20457 0 0 09000064b962e86b
USDA_FRDOC_0001-3376 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-06T04:00:00Z 2026 10 2026-10-06T04:00:00Z   2026-10-06T17:03:19Z 2026-20449 0 0 09000064b962e6ed
EPA_FRDOC_0001-33194 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Environmental Impact Statements; Availability, etc. Notice   2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T16:26:05Z 2026-20240 0 0 09000064b96047fa
FDA-2025-N-1927-0104 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2024 FDA-2025-N-1927 GRAS Notice (GRN) 1241 – Amendments – beta-lactoglobulin produced by Aspergillus oryzae Notice General Notice 2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T23:48:52Z   0 0 09000064b95fccd7
FDA-2025-N-1928-0079 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2025 FDA-2025-N-1928 GRAS Notice (GRN) 1251 – Amendment – Saccharomyces cerevisiae expressing a gene encoding a cysteine-thiol lyase from Staphylococcus hominis (S. cerevisiae "OYR-290") Notice General Notice 2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T23:49:37Z   0 0 09000064b95fccda
FDA-2025-N-1927-0103 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2024 FDA-2025-N-1927 GRAS Notice (GRN) 1237 – Amendment – beta-glucanase enzyme preparation produced by Talaromyces versatilis Notice General Notice 2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T23:48:16Z   0 0 09000064b95fccd6
FDA-2025-N-1928-0080 FDA Generally Recognized as Safe (GRAS) Notices Filed in 2025 FDA-2025-N-1928 GRAS Notice (GRN) 1252 – Amendments – Saccharomyces cerevisiae "BY-1568" Notice General Notice 2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T23:49:59Z   0 0 09000064b95fccdb
USDA_FRDOC_0001-3375 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T16:25:39Z 2026-20267 0 0 09000064b96046d0
USDA_FRDOC_0001-3373 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T16:25:30Z 2026-20278 0 0 09000064b9604628
USDA_FRDOC_0001-3374 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-10-02T04:00:00Z 2026 10 2026-10-02T04:00:00Z   2026-10-02T16:25:35Z 2026-20237 0 0 09000064b960467d
FDA-2026-N-6876-0005 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Devices; Voluntary Improvement Program FDA-2026-N-6876 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Voluntary Improvement Program Notice 30 Day Proposed Information Collection 2026-10-01T04:00:00Z 2026 10 2026-10-01T04:00:00Z 2026-11-03T04:59:59Z 2026-10-01T17:10:26Z 2026-20085 1 0 09000064b95fa835
FDA-2026-N-0008-0014 FDA Advisory Committee FDA-2026-N-0008 Request for Nominations for Individuals and Consumer Organizations for Advisory Committees Notice Request for Nominations 2026-10-01T04:00:00Z 2026 10 2026-10-01T04:00:00Z   2026-10-01T17:17:08Z 2026-20065 0 0 09000064b95fa717
FDA-2026-N-0008-0016 FDA Advisory Committee FDA-2026-N-0008 Request for Nominations for Voting Members of Food and Drug Administration Advisory Committees Notice Request for Nominations 2026-10-01T04:00:00Z 2026 10 2026-10-01T04:00:00Z   2026-10-01T17:22:06Z 2026-20063 0 0 09000064b95f234b
FDA-2026-N-0008-0015 FDA Advisory Committee FDA-2026-N-0008 Advisory Committee; Antimicrobial Drugs Advisory Committee; Renewal Notice Notice of Renewal 2026-10-01T04:00:00Z 2026 10 2026-10-01T04:00:00Z   2026-10-01T17:19:17Z 2026-20142 0 0 09000064b95fa69a
FDA-2026-N-0008-0013 FDA Advisory Committee FDA-2026-N-0008 Advisory Committee; Dermatologic and Ophthalmic Drugs Advisory Committee; Renewal Notice Notice of Renewal 2026-10-01T04:00:00Z 2026 10 2026-10-01T04:00:00Z   2026-10-01T17:14:19Z 2026-20141 0 0 09000064b95fa7f1
EPA_FRDOC_0001-33186 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Public Water System Supervision Program: State of Illinois; Approval Notice   2026-09-30T04:00:00Z 2026 9 2026-09-30T04:00:00Z   2026-09-30T23:02:08Z 2026-19976 0 0 09000064b95f22fc
EPA_FRDOC_0001-33187 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Hearings, Meetings, Proceedings, etc.: Science Advisory Board Notice   2026-09-30T04:00:00Z 2026 9 2026-09-30T04:00:00Z   2026-09-30T20:10:24Z 2026-20057 0 0 09000064b95f2301
EPA-HQ-OAR-2026-4358-0007 EPA Information Collection Request: Renewable Fuel Standard (RFS) Program: Reporting and Recordkeeping Requirements for Biogas Regulatory Reform EPA-HQ-OAR-2026-4358 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Renewable Fuel Standard Program: Standards for 2023-2025 and Other Changes Notice Information Collection Request (ICR) 2026-09-30T04:00:00Z 2026 9 2026-09-30T04:00:00Z 2026-10-31T03:59:59Z 2026-09-30T19:40:12Z 2026-20053 1 0 09000064b95f217a
FDA-2026-P-4574-0003 FDA Requests that the FDA determine whether the original formulation submitted for the Reference Listed Drng (RLD), ISTURSIA (osilodrostat) tablets 10 mg (Product Number 003); New Drug Application (NDA) 212801, held by RECORDATI RARE DISEASES INC has been voluntarily withdrawn from the commercial market or withdrawn from sale for reasons of safety or eff FDA-2026-P-4574 Determination That ISTURISA (Osilodrostat) Tablets, 10 Milligrams, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice Determinations 2026-09-30T04:00:00Z 2026 9 2026-09-30T04:00:00Z   2026-09-30T20:10:10Z 2026-19968 0 0 09000064b95f22ff
FWS-HQ-NWRS-2025-1397-0006 FWS Agency Information Collection Activities; Interjurisdictional Invasive Species Rapid Response Program FWS-HQ-NWRS-2025-1397 Agency Information Collection Activities; Interjurisdictional Invasive Species Rapid Response Team Program Notice   2026-09-30T04:00:00Z 2026 9 2026-09-30T04:00:00Z 2026-12-01T04:59:59Z 2026-10-14T09:00:59Z 2026-19969 1 0 09000064b95f29b2
FDA-2026-N-10132-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Protection of Human Subjects and Institutional Review Boards FDA-2026-N-10132 Agency Information Collection Activities; Proposed Collection; Comment Request; Protection of Human Subjects and Institutional Review Boards Notice 60 Day Proposed Information Collection 2026-09-29T04:00:00Z 2026 9 2026-09-29T04:00:00Z 2026-12-01T04:59:59Z 2026-09-29T17:15:35Z 2026-19849 1 0 09000064b95e7083
FDA-2025-P-0394-0004 FDA Request that FDA determine whether the Reference Listed Drug (RLD), Sulfadiazine Tablets, 500 mg under New Drug Application (NDA) 004122 held by Eli Lilly and Co., was voluntarily withdrawn from commercial distribution or withdrawn from sale for safety or efficacy reasons. FDA-2025-P-0394 Determination That SULFADIAZINE (Sulfadiazine) Tablet, 500 Milligrams, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice Determinations 2026-09-29T04:00:00Z 2026 9 2026-09-29T04:00:00Z   2026-09-29T17:20:40Z 2026-19921 0 0 09000064b95e707d
FDA-2026-N-2743-0003 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission of Information to a Master File in Support of Petitions; and Electronic Submission Using Food and Drug Administration Form 3503 FDA-2026-N-2743 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission of Information to a Master File in Support of Petitions; and Electronic Submission Using Food and Drug Administration Form 3503 Notice 30 Day Proposed Information Collection 2026-09-29T04:00:00Z 2026 9 2026-09-29T04:00:00Z 2026-10-30T03:59:59Z 2026-09-29T17:13:03Z 2026-19850 1 0 09000064b95e920c
FDA-2026-N-10505-0001 FDA FHTA LLC; Withdrawal of Approval of New Drug Application for Mysoline (Primidone) Suspension, 250 Milligrams/5 Milliliters FDA-2026-N-10505 FHTA LLC; Withdrawal of Approval of New Drug Application for MYSOLINE (Primidone) Suspension, 250 Milligrams/5 Milliliters Notice Withdrawal 2026-09-29T04:00:00Z 2026 9 2026-09-29T04:00:00Z   2026-09-29T17:09:02Z 2026-19912 0 0 09000064b95e92f9
USDA_FRDOC_0001-3372 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-09-29T04:00:00Z 2026 9 2026-09-29T04:00:00Z   2026-09-29T16:25:38Z 2026-19862 0 0 09000064b95e911b
EPA-HQ-OPP-2017-0751-0044 EPA Registration Review Interim Decisions; Notice of Availability EPA-HQ-OPP-2017-0751 Pesticide Registration Review: 4-CPA Final Decision Notice   2026-09-28T04:00:00Z 2026 9 2026-09-28T04:00:00Z   2026-09-28T17:39:02Z 2026-19744 0 0 09000064b95d3073
EPA-HQ-OPP-2014-0544-0017 EPA 4-chlorophenoxyacetic acid (4-CPA) – Combined Work Plan, Summary Document, and Proposed Interim Registration Review Decision. Case Number 2115. EPA-HQ-OPP-2014-0544 Pesticide Registration Review: 4-CPA Final Decision Notice   2026-09-28T04:00:00Z 2026 9 2026-09-28T04:00:00Z   2026-09-28T17:34:56Z 2026-19744 0 0 09000064b95d727e
EPA-R06-OAR-2026-1323-0002 EPA Blue Marlin Offshore Port LLC (BMOP) - Deepwater Port (DWP), Proposed PSD Permit R6 PSD-DWP-GA10 and Proposed Title V Permit R6T5-DWP-GA10 EPA-R06-OAR-2026-1323 02. Public Notice Documents Notice   2026-09-28T04:00:00Z 2026 9 2026-09-29T04:00:00Z 2026-10-30T03:59:59Z 2026-09-29T15:54:43Z   1 0 09000064b91a7613
EPA-HQ-OPP-2009-0361-14478 EPA Glyphosate Registration Review EPA-HQ-OPP-2009-0361 Glyphosate Open Literature Search to Inform Human Health Risk Assessment Notice   2026-09-28T04:00:00Z 2026 9 2026-09-28T04:00:00Z   2026-09-28T18:28:22Z 2026-19775 0 0 09000064b95d7125
EPA_FRDOC_0001-33176 EPA Recently Posted EPA Rules and Notices from FR Feed. EPA_FRDOC_0001 Environmental Impact Statements; Availability, etc. Notice   2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z   2026-09-25T16:25:48Z 2026-19676 0 0 09000064b95c5450
FDA-2025-N-6692-0002 FDA NOOH Proposal to Debar Jeffrey Thies FDA-2025-N-6692 Jeffrey Thies: Final Debarment Order Notice Statutory Debarment 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z   2026-09-25T22:46:01Z 2026-19655 1 0 09000064b95c54e1
FDA-2026-N-9505-0001 FDA Robotically-Assisted Surgical Devices – Premarket Submissions; Draft Guidance for Industry and Food and Drug Administration Staff; Availability FDA-2026-N-9505 Robotically-Assisted Surgical Devices—Premarket Submissions; Draft Guidance for Industry and Food and Drug Administration Staff; Availability Notice Notice of Availability 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z 2026-11-25T04:59:59Z 2026-09-25T19:21:13Z 2026-19704 1 0 09000064b95c549b
FDA-2026-N-10606-0001 FDA Dermatologic and Ophthalmic Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments—New Drug Application (NDA) 219694 for atropine sulfate ophthalmic solution, 0.01% FDA-2026-N-10606 Dermatologic and Ophthalmic Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments—New Drug Application (NDA) 219694 for Atropine Sulfate Ophthalmic Solution, 0.01% Notice Request for Comments 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z 2026-10-30T03:59:59Z 2026-10-15T09:00:38Z 2026-19700 1 0 09000064b95c540b
FDA-2026-C-10597-0001 FDA Filing of Color Additive Petition from Doehler GmbH; Request to Amend the Color Additive Regulations to Provide for the Safe Use of Calcium Sulfate in Various Foods at Levels Consistent with Good Manufacturing Practice FDA-2026-C-10597 Filing of Color Additive Petition From Doehler GmbH; Request To Amend the Color Additive Regulations To Provide for the Safe Use of Calcium Sulfate in Various Foods at Levels Consistent With Good Manufacturing Practice Notice Announcement 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z   2026-10-02T21:57:29Z 2026-19658 0 0 09000064b95c6531
FDA-2025-N-7395-0002 FDA Proposal to Debar Naveed Aslam FDA-2025-N-7395 Naveed Aslam: Final Debarment Order Notice Statutory Debarment 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z   2026-09-25T20:59:18Z 2026-19654 1 0 09000064b95c6607
FDA-2015-N-3326-0056 FDA Biosimilar User Fee Act FDA-2015-N-3326 Reauthorization of the Biosimilar User Fee Act; Public Meeting; Request for Comments Notice Request for Comments 2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z 2026-11-26T04:59:59Z 2026-10-06T09:00:35Z 2026-19660 1 0 09000064b95c53b7
USDA_FRDOC_0001-3371 USDA Recently Posted USDA Rules and Notices. USDA_FRDOC_0001 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice   2026-09-25T04:00:00Z 2026 9 2026-09-25T04:00:00Z   2026-09-25T16:26:06Z 2026-19629 0 0 09000064b95c6537
EPA-HQ-OAR-2021-0124-0004 EPA NESHAP for Aluminum, Copper, and Other Non-Ferrous Foundries (40 CFR part 63, subpart ZZZZZZ) (Renewal) EPA-HQ-OAR-2021-0124 Agency Information Collection Activities; Proposals, Submissions, and Approvals: National Emission Standards for Hazardous Air Pollutants for Aluminum, Copper, and Other Non-Ferrous Foundries Notice Information Collection Request (ICR) 2026-09-24T04:00:00Z 2026 9 2026-09-24T04:00:00Z 2026-10-27T03:59:59Z 2026-09-25T09:00:33Z 2026-19505 1 0 09000064b95bf69e
EPA-HQ-OW-2026-4852-0009 EPA Agency Information Collection Activities: Proposed Collection; Comment Request; Information Collection Request (ICR) for State Source Water Protection Programs EPA-HQ-OW-2026-4852 Agency Information Collection Activities; Proposals, Submissions, and Approvals: EPA Program Information on Source Water Protection (Renewal) Notice Information Collection Request (ICR) 2026-09-24T04:00:00Z 2026 9 2026-09-24T04:00:00Z 2026-10-27T03:59:59Z 2026-09-24T16:40:03Z 2026-19502 1 0 09000064b95bf727
EPA-HQ-OAR-2021-0098-0005 EPA NESHAP for the Surface Coating of Large Household and Commercial Appliances (40 CFR part 63, subpart NNNN) (Renewal) EPA-HQ-OAR-2021-0098 Agency Information Collection Activities; Proposals, Submissions, and Approvals: NESHAP for the Surface Coating of Large Household and Commercial Appliances Notice Information Collection Request (ICR) 2026-09-24T04:00:00Z 2026 9 2026-09-24T04:00:00Z 2026-10-27T03:59:59Z 2026-09-24T16:45:04Z 2026-19499 1 0 09000064b95bf652
EPA-R06-OAR-2021-0029-0114 EPA TX249 Texas Agreed Orders Regarding Planned Maintenance, Startup And Shutdown Emissions For Certain Electric Generating Units, submitted to EPA August 20, 2020 (TX-453, SIP) EPA-R06-OAR-2021-0029 TX249x114 Notice of Availability for Public Comment; Reconsideration of Air Plan Disapproval: Texas; Control of Air Pollution from Visible Emissions and Particulate Matter. 3 pages Notice   2026-09-24T04:00:00Z 2026 9 2026-09-24T04:00:00Z 2026-10-27T03:59:59Z 2026-10-13T09:01:00Z 2026-19496 1 0 09000064b95bf723
EPA-HQ-OAR-2021-0105-0005 EPA NESHAP for Semiconductor Manufacturing (40 CFR part 63, Subpart BBBBB) (Renewal) EPA-HQ-OAR-2021-0105 Agency Information Collection Activities; Proposals, Submissions, and Approvals: NESHAP for Semiconductor Manufacturing Notice Information Collection Request (ICR) 2026-09-24T04:00:00Z 2026 9 2026-09-24T04:00:00Z 2026-10-27T03:59:59Z 2026-09-24T16:35:01Z 2026-19504 1 0 09000064b95bf763

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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);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;
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