Currently Open for Comment
| id | agency_id | title | document_type | posted_date | comment_start_date | comment_end_date | docket_id | days_remaining | comments_so_far |
|---|---|---|---|---|---|---|---|---|---|
| EPA-HQ-OPPT-2018-0446-0083 | EPA | o-Dichlorobenzene and p-Dichlorobenzene; Draft Risk Evaluations Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comment | Notice | 2026-08-10T04:00:00Z | 2026-08-10T04:00:00Z | 2026-10-10T03:59:59Z | EPA-HQ-OPPT-2018-0446 | 1 | 35 |
| EPA-HQ-OPPT-2018-0444-0074 | EPA | o-Dichlorobenzene and p-Dichlorobenzene; Draft Risk Evaluations Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comment | Notice | 2026-08-10T04:00:00Z | 2026-08-10T04:00:00Z | 2026-10-10T03:59:59Z | EPA-HQ-OPPT-2018-0444 | 1 | 34 |
| EPA-HQ-OFA-2026-2542-0001 | EPA | Agency Information Collection Activities; Proposals, Submissions, and Approvals: General Performance Reporting for Assistance Programs, Promoting Readiness and Enhancing Proficiency to Advance Reporting and Data, and National Estuary Program | Notice | 2026-09-09T04:00:00Z | 2026-09-09T04:00:00Z | 2026-10-10T03:59:59Z | EPA-HQ-OFA-2026-2542 | 1 | 0 |
| EPA-R08-OAR-2023-0495-0065 | EPA | Air Quality State Implementation Plans; Approvals and Promulgations: North Dakota; Reconsideration and Repeal of Air Plan Partial Approval and Partial Disapproval of Regional Haze State Implementation Plan for the Second Implementation Period | Proposed Rule | 2026-09-09T04:00:00Z | 2026-09-09T04:00:00Z | 2026-10-10T03:59:59Z | EPA-R08-OAR-2023-0495 | 1 | 31 |
| EPA-HQ-OW-2025-0322-15447 | EPA | Updated Definition of “Waters of the United States” | Proposed Rule | 2026-09-09T04:00:00Z | 2026-09-09T04:00:00Z | 2026-10-10T03:59:59Z | EPA-HQ-OW-2025-0322 | 1 | 15338 |
| FDA-2025-E-5206-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BRINSUPRI | Notice | 2026-08-10T04:00:00Z | 2026-08-10T04:00:00Z | 2026-10-10T03:59:59Z | FDA-2025-E-5206 | 1 | 0 |
| FDA-2026-N-7630-0001 | FDA | Radiology Devices; Reclassification of Digital Breast Tomosynthesis System | Proposed Rule | 2026-08-10T04:00:00Z | 2026-08-10T04:00:00Z | 2026-10-10T03:59:59Z | FDA-2026-N-7630 | 1 | 1 |
| FDA-2025-E-0707-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; DAYVIGO | Notice | 2026-08-10T04:00:00Z | 2026-08-10T04:00:00Z | 2026-10-10T03:59:59Z | FDA-2025-E-0707 | 1 | 0 |
| FDA-2026-N-9737-0001 | FDA | Notice of Data Availability and Announcement of Open Public Comment Period: Pharmacokinetics and Safety of Commonly Used Drugs in Lactating Women and Breastfed Infants - Nifedipine | Other | 2026-09-11T04:00:00Z | 2026-09-11T04:00:00Z | 2026-10-13T03:59:59Z | FDA-2026-N-9737 | 4 | 0 |
| APHIS-2026-0265-0001 | APHIS | Petition for a Determination of Nonregulated Status and Draft Plant Pest Risk Assessment: Early and Near-Continuous Blooming European Plum (Prunus domestica) Lines (34 plum and 157 plum) | Notice | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-14T03:59:59Z | APHIS-2026-0265 | 5 | 3 |
| EPA-HQ-OLEM-2026-4159-0001 | EPA | Hazardous and Solid Waste Management System: Disposal of Coal Combustion Residuals from Electric Utilities; Federal CCR Permit Program; General Permit Provisions | Proposed Rule | 2026-07-14T04:00:00Z | 2026-07-14T04:00:00Z | 2026-10-14T03:59:59Z | EPA-HQ-OLEM-2026-4159 | 5 | 1 |
| EPA-HQ-OPPT-2025-2433-0001 | EPA | 2026 Unified Agenda of Regulatory and Deregulatory Actions | Notice | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-14T03:59:59Z | EPA-HQ-OPPT-2025-2433 | 5 | 1 |
| EPA-HQ-OLEM-2025-3225-0001 | EPA | 2026 Unified Agenda of Regulatory and Deregulatory Actions | Notice | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-14T03:59:59Z | EPA-HQ-OLEM-2025-3225 | 5 | 1 |
| EPA-HQ-OAR-2025-3160-0001 | EPA | 2026 Unified Agenda of Regulatory and Deregulatory Actions | Notice | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-14T03:59:59Z | EPA-HQ-OAR-2025-3160 | 5 | 1 |
| EPA-HQ-OPPT-2015-0436-0048 | EPA | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Generic Clearance for TSCA Section 4 Test Rules, Test Orders, Enforceable Consent Agreements, Voluntary Data Submissions, and Exemptions from Testing Requirement (Renewal) | Notice | 2026-08-11T04:00:00Z | 2026-08-11T04:00:00Z | 2026-10-14T03:59:59Z | EPA-HQ-OPPT-2015-0436 | 5 | 11 |
| FDA-2026-D-7957-0002 | FDA | Container Closure Systems for Human Drugs and Biological Products; Guidance for Industry - Draft Guidance | Other | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-14T03:59:59Z | FDA-2026-D-7957 | 5 | 6 |
| FDA-2016-N-3120-0570 | FDA | Kremers Urban Pharmaceuticals, Inc.; Grant of Hearing Request Regarding a Proposal To Withdraw Approval of an Abbreviated New Drug Application for Extended-Release Methylphenidate Tablets | Notice | 2026-08-13T04:00:00Z | 2026-08-13T04:00:00Z | 2026-10-14T03:59:59Z | FDA-2016-N-3120 | 5 | 4 |
| FDA-2026-N-2917-0002 | FDA | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Generic Clearance for Qualitative Data To Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed | Notice | 2026-09-11T04:00:00Z | 2026-09-11T04:00:00Z | 2026-10-14T03:59:59Z | FDA-2026-N-2917 | 5 | 0 |
| FWS-HQ-MB-2026-2146-0001 | FWS | Agency Information Collection Activities; Federal Fish and Wildlife Permit Applications and Reports-Migratory Birds | Notice | 2026-08-13T04:00:00Z | 2026-08-13T04:00:00Z | 2026-10-14T03:59:59Z | FWS-HQ-MB-2026-2146 | 5 | 0 |
| FWS-R8-ES-2026-2971-0001 | FWS | Receipt of Incidental Take Permit Application and Proposed Habitat Conservation Plan for Woodward 46 Specific Plan Project, City of San Marcos, CA; Categorical Exclusion | Notice | 2026-09-11T04:00:00Z | 2026-09-11T04:00:00Z | 2026-10-14T03:59:59Z | FWS-R8-ES-2026-2971 | 5 | 0 |
| USDA_FRDOC_0001-3365 | USDA | Request for Information: Modernization of Regulations | Proposed Rule | 2026-09-11T04:00:00Z | 2026-09-11T04:00:00Z | 2026-10-14T03:59:59Z | USDA_FRDOC_0001 | 5 | 2 |
| EPA-R09-OAR-2026-4885-0001 | EPA | Clean Data Determination; 1997 8-hour Ozone Standards; California; Sacramento Metro Area | Proposed Rule | 2026-09-14T04:00:00Z | 2026-09-14T04:00:00Z | 2026-10-15T03:59:59Z | EPA-R09-OAR-2026-4885 | 6 | 0 |
| EPA-R03-OAR-2026-4522-0001 | EPA | State Plans for Designated Facilities and Pollutants; Approvals and Promulgations: District of Columbia; Negative Declaration for Existing Other Solid Waste Incinerators | Proposed Rule | 2026-09-14T04:00:00Z | 2026-09-14T04:00:00Z | 2026-10-15T03:59:59Z | EPA-R03-OAR-2026-4522 | 6 | 0 |
| EPA-R03-OAR-2026-4225-0001 | EPA | State Plans for Designated Facilities and Pollutants; Approvals and Promulgations: Maryland; Negative Declaration for Existing Other Solid Waste Incinerators | Proposed Rule | 2026-09-14T04:00:00Z | 2026-09-14T04:00:00Z | 2026-10-15T03:59:59Z | EPA-R03-OAR-2026-4225 | 6 | 0 |
| FDA-2026-N-2740-0003 | FDA | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Customer/Partner Customer Service Satisfaction Surveys | Notice | 2026-09-14T04:00:00Z | 2026-09-14T04:00:00Z | 2026-10-15T03:59:59Z | FDA-2026-N-2740 | 6 | 1 |
| EPA-R09-OAR-2021-0864-0006 | EPA | Draft Permit for Cache Creek Casino Resort | Other | 2026-09-15T04:00:00Z | 2026-09-15T04:00:00Z | 2026-10-16T03:59:59Z | EPA-R09-OAR-2021-0864 | 7 | 0 |
| FWS-HQ-IA-2026-3070-0001 | FWS | Foreign Endangered Species; Receipt of Permit Applications | Notice | 2026-09-15T04:00:00Z | 2026-09-15T04:00:00Z | 2026-10-16T03:59:59Z | FWS-HQ-IA-2026-3070 | 7 | 0 |
| EPA-HQ-OPP-2022-0743-0004 | EPA | Pesticide Tolerance; Exemptions, Petitions, Revocations, etc.: Calcium Carbonate | Rule | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | EPA-HQ-OPP-2022-0743 | 8 | 3 |
| FDA-2026-N-8328-0001 | FDA | Agency Information Collection Activities; Proposed Collection; Comment Request; Imports and Electronic Import Entries | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2026-N-8328 | 8 | 0 |
| FDA-2025-E-0486-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BIZENGRI | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-E-0486 | 8 | 0 |
| FDA-2025-E-0488-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BIZENGRI | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-E-0488 | 8 | 0 |
| FDA-2026-N-7757-0001 | FDA | Agency Information Collection Activities; Proposed Collection; Comment Request; Third Party Disclosure and Recordkeeping Requirements for Reportable Food | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2026-N-7757 | 8 | 0 |
| FDA-2026-N-8249-0001 | FDA | Gastroenterology-Urology Devices; Reclassification of Diagnostic Endoscopic Light Source Systems To Be Renamed Cystoscopic Systems Intended as an Aid for Detection of Bladder Cancer | Proposed Rule | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2026-N-8249 | 8 | 1 |
| FDA-2025-E-0490-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BIZENGRI | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-E-0490 | 8 | 0 |
| FDA-2025-N-6224-0011 | FDA | Medical Devices; Classification of Accessories Distinct From Other Devices; Proposed List of Accessories Suitable for Class I; Request for Comments | Proposed Rule | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-N-6224 | 8 | 8 |
| FDA-2025-E-0485-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BIZENGRI | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-E-0485 | 8 | 0 |
| FDA-2025-E-0489-0005 | FDA | Determination of Regulatory Review Period for Purposes of Patent Extension; BIZENGRI | Notice | 2026-08-17T04:00:00Z | 2026-08-17T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2025-E-0489 | 8 | 0 |
| FDA-2026-N-8163-0001 | FDA | Reauthorization of the Prescription Drug User Fee Act; Public Meeting; Request for Comments | Notice | 2026-08-14T04:00:00Z | 2026-08-14T04:00:00Z | 2026-10-17T03:59:59Z | FDA-2026-N-8163 | 8 | 3 |
| FDA-2025-N-0873-0014 | FDA | Reauthorization of the Generic Drug User Fee Amendments; Public Meeting; Request for Comments | Notice | 2026-08-11T04:00:00Z | 2026-08-11T04:00:00Z | 2026-10-18T03:59:59Z | FDA-2025-N-0873 | 9 | 14 |
| APHIS-2026-1090-0001 | APHIS | Petition: Pioneer Hi-Bred International, Inc.; Determination of Nonregulated Status and Draft Plant Pest Risk Assessment for Insect Resistant COR-23134-4 Soybean (Glycine max) | Notice | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | APHIS-2026-1090 | 11 | 3 |
| APHIS-2026-1354-0001 | APHIS | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Animal Care; Standards for Birds Not Bred for Use in Research under the Animal Welfare Act | Notice | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | APHIS-2026-1354 | 11 | 0 |
| EPA-HQ-OPP-2024-0548-0003 | EPA | Pesticide Tolerance; Exemptions, Petitions, Revocations, etc.: Cypermethrin | Rule | 2026-08-20T04:00:00Z | 2026-08-20T04:00:00Z | 2026-10-20T03:59:59Z | EPA-HQ-OPP-2024-0548 | 11 | 0 |
| EPA-HQ-OPPT-2018-0488-0065 | EPA | Ethylene Dibromide Draft Risk Evaluation Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comment | Notice | 2026-08-19T04:00:00Z | 2026-08-19T04:00:00Z | 2026-10-20T03:59:59Z | EPA-HQ-OPPT-2018-0488 | 11 | 32 |
| EPA-HQ-OW-2026-6965-0001 | EPA | Updates to the National Pollutant Discharge Elimination System Definitions and Exclusions | Proposed Rule | 2026-09-04T04:00:00Z | 2026-09-04T04:00:00Z | 2026-10-20T03:59:59Z | EPA-HQ-OW-2026-6965 | 11 | 16 |
| FDA-2017-D-5974-0013 | FDA | Determining Whether to Submit an ANDA or a 505(b)(2) Application; Guidance for Industry; Draft Guidance | Other | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | FDA-2017-D-5974 | 11 | 6 |
| FDA-2017-D-5974-0012 | FDA | Determining Whether To Submit an ANDA or a 505(b)(2) Application; Draft Guidance for Industry; Availability | Notice | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | FDA-2017-D-5974 | 11 | 6 |
| FDA-2026-N-5479-0001 | FDA | Testosterone Use in Menopausal Women; Public Workshop; Request for Comments | Notice | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | FDA-2026-N-5479 | 11 | 1072 |
| FDA-2026-N-7874-0001 | FDA | Considerations for the Regulation of Generative AI-Enabled Medical Devices: Discussion Paper and Request for Feedback | Other | 2026-08-18T04:00:00Z | 2026-08-18T04:00:00Z | 2026-10-20T03:59:59Z | FDA-2026-N-7874 | 11 | 98 |
| EPA-HQ-OW-2014-0359-0042 | EPA | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Information Request for the Underground Injection Control Program | Notice | 2026-08-21T04:00:00Z | 2026-08-21T04:00:00Z | 2026-10-21T03:59:59Z | EPA-HQ-OW-2014-0359 | 12 | 5 |
| EPA-HQ-OPP-2022-0455-0011 | EPA | Pesticide Tolerances: Carboxin | Rule | 2026-08-21T04:00:00Z | 2026-08-21T04:00:00Z | 2026-10-21T03:59:59Z | EPA-HQ-OPP-2022-0455 | 12 | 2 |
| FDA-2007-D-0369-2640 | FDA | Product-Specific Guidances; Draft and Revised Draft Guidances for Industry; Availability | Notice | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2657 | FDA | PSG_218475 - Draft Guidance on Epinephrine Bitartrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2673 | FDA | PSG_214662 - Draft Guidance on Maralixibat Chloride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2674 | FDA | PSG_217593 - Draft Guidance on Meloxicam | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2687 | FDA | PSG_020573 - Draft Guidance on Sodium Phenylbutyrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2689 | FDA | PSG_219839 - Draft Guidance on Sunvozertinib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2654 | FDA | PSG_204370 - Draft Guidance on Cariprazine Hydrochloride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2659 | FDA | PSG_022180 - Draft Guidance on Ferumoxytol | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2661 | FDA | PSG_020496 - Draft Guidance on Glimepiride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2662 | FDA | PSG_213876 - Draft Guidance on Hydrocortisone | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2664 | FDA | PSG_209939 - Draft Guidance on Letermovir | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2668 | FDA | PSG_021924 - Draft Guidance on Levothyroxine Sodium | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2686 | FDA | PSG_219301 - Draft Guidance on Sebetralstat | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2642 | FDA | PSG_208147 - Draft Guidance on Amphetamine; Amphetamine Aspartate/Dextroamphetamine Sulfate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2646 | FDA | PSG_214510 - Draft Guidance on Benzoyl Peroxide | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2663 | FDA | PSG_206185 - Draft Guidance on Latanoprost | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2667 | FDA | PSG_021731 - Draft Guidance on Leuprolide Acetate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2671 | FDA | PSG_219847 - Draft Guidance on Lisdexamfetamine Dimesylate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2679 | FDA | PSG_203340 - Draft Guidance on Nimodipine | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2681 | FDA | PSG_208558 - Draft Guidance on Olaparib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2685 | FDA | PSG_219685 - Draft Guidance on Rilzabrutinib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2641 | FDA | PSG_204325 - Draft Guidance on Amphetamine | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2649 | FDA | PSG_217729 - Draft Guidance on Bosutinib Monohydrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2650 | FDA | PSG_217673 - Draft Guidance on Brensocatib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2652 | FDA | PSG_020816 - Draft Guidance on Brinzolamide | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2655 | FDA | PSG_050600 - Draft Guidance on Clindamycin Phosphate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2660 | FDA | PSG_020243 - Draft Guidance on Fluvoxamine Maleate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2675 | FDA | PSG_218395 - Draft Guidance on Meloxicam | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2676 | FDA | PSG_215211 - Draft Guidance on Miglustat | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2680 | FDA | PSG_021008 - Draft Guidance on Octreotide Acetate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2690 | FDA | PSG_219713 - Draft Guidance on Taletrectinib Adipate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2691 | FDA | PSG_211801 - Draft Guidance on Tenapanor Hydrochloride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2695 | FDA | PSG_022328 - Draft Guidance on Zolpidem Tartrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2643 | FDA | PSG_210526 - Draft Guidance on Amphetamine;Amphetamine Aspartate/Dextroamphetamine Sulfate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2647 | FDA | PSG_214902 - Draft Guidance on Benzoyl Peroxide; Tretinoin | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2656 | FDA | PSG_215425 - Draft Guidance on Epinephrine | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2658 | FDA | PSG_203565 - Draft Guidance on Ferric Carboxymaltose | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2665 | FDA | PSG_021343 - Draft Guidance on Leuprolide Acetate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2669 | FDA | PSG_215029 - Draft Guidance on Lidocaine | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2670 | FDA | PSG_021977 - Draft Guidance on Lisdexamfetamine Dimesylate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2672 | FDA | PSG_219485 - Draft Guidance on Maralixibat Chloride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2677 | FDA | PSG_020415 - Draft Guidance on Mirtazapine | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2678 | FDA | PSG_215793 - Draft Guidance on Mitomycin | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2683 | FDA | PSG_020781 - Draft Guidance on Ondansetron | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2684 | FDA | PSG_211150 - Draft Guidance on Pitolisant Hydrochloride | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2688 | FDA | PSG_214860 - Draft Guidance on Sodium Phenylbutyrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2692 | FDA | PSG_219304 - Draft Guidance on Vimseltinib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2693 | FDA | PSG_021774 - Draft Guidance on Zolpidem Tartrate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2644 | FDA | PSG_219696 - Draft Guidance on Avatrombopag Maleate | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |
| FDA-2007-D-0369-2645 | FDA | PSG_207924 - Draft Guidance on Baricitinib | Other | 2026-08-24T04:00:00Z | 2026-08-24T04:00:00Z | 2026-10-24T03:59:59Z | FDA-2007-D-0369 | 15 | 560 |