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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

669 rows where agency_id = "FDA", document_type = "Notice" and posted_year = 2007 sorted by posted_date descending

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posted_year 1

  • 2007 · 669 ✖

document_type 1

  • Notice · 669 ✖

agency_id 1

  • FDA · 669 ✖
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2007-D-0257-0001 FDA None FDA-2007-D-0257 See Document ID FDA-2007-D-0257-0003 Notice   2007-12-28T00:00:00Z 2007 12     2008-05-21T20:22:03Z   0 1 090000648042b1c1
FDA-2007-N-0313-0001 FDA None FDA-2007-N-0313 Maximizing the Public Health Benefit of Adverse Event Collection Throughout a Product's Marketed Life Cycle; Public Workshop; Request for Comments Notice NM-Notice of Meeting 2007-12-26T05:00:00Z 2007 12 2007-12-21T05:00:00Z 2008-03-01T04:59:59Z 2008-08-15T01:38:12Z   0 0 090000648042b70a
FDA-2007-N-0441-0001 FDA None FDA-2007-N-0441 Agency Emergency Processing Under the Office of Management and Budget Review; Certification to Accompany Drug, Biological Product, and Device Applications or Submissions; Correction Notice Correction 2007-12-26T05:00:00Z 2007 12     2025-08-19T20:11:21Z E7-24914 0 0 090000648042dda7
FDA-2007-C-0044-0001 FDA None FDA-2007-C-0044 DSM Nutritional Products, Inc.; Filing of Color Additive Petition; Correction Notice NCR-Notice of Correction 2007-12-26T05:00:00Z 2007 12 2007-12-21T05:00:00Z   2026-01-08T20:18:17Z   0 0 0900006480429648
FDA-2007-N-0152-0001 FDA None FDA-2007-N-0152 Health Claims and Qualified Health Claims; Dietary Lipids and Cancer, Soy Protein and Coronary Heart Disease, Antioxidant Vitamins and Certain Cancers, and Selenium and Certain Cancers; Reevaluation; Opportunity for Public Comment Notice N-Notice 2007-12-21T05:00:00Z 2007 12 2007-12-21T05:00:00Z 2008-02-20T04:59:59Z 2008-07-08T18:53:47Z   0 0 090000648042a409
FDA-2007-M-0452-0001 FDA None FDA-2007-M-0452 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-09T22:48:41Z E7-24620 0 0 090000648042dec7
FDA-2007-M-0273-0001 FDA None FDA-2007-M-0273 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-09T21:15:57Z E7-24620 0 0 090000648042b3c6
FDA-2007-M-0453-0001 FDA None FDA-2007-M-0453 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-10T00:23:52Z E7-24620 0 0 090000648042ded7
FDA-2007-M-0325-0001 FDA None FDA-2007-M-0325 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-10T04:01:42Z E7-24620 0 0 090000648042b804
FDA-2007-N-0382-0001 FDA None FDA-2007-N-0382 Cellular, Tissue and Gene Therapies Advisory Committee; Notice of Meeting Notice Meeting 2007-12-19T05:00:00Z 2007 12     2025-08-19T15:55:54Z E7-24629 0 0 090000648042d70f
FDA-2007-M-0397-0001 FDA None FDA-2007-M-0397 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-12T23:22:10Z E7-24620 0 0 090000648042d84e
FDA-2007-M-0224-0001 FDA None FDA-2007-M-0224 FDA Notice NAL-Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2008-04-04T00:35:16Z   0 0 090000648042ae2e
FDA-2007-M-0223-0001 FDA None FDA-2007-M-0223 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-09T23:33:10Z E7-24620 0 0 090000648042ae1d
FDA-2007-M-0093-0001 FDA None FDA-2007-M-0093 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications Notice Notice of Approval 2007-12-19T05:00:00Z 2007 12 2007-12-19T05:00:00Z   2026-01-13T00:37:18Z E7-24620 0 0 0900006480429d20
FDA-2007-D-0306-0002 FDA None FDA-2007-D-0306 International Conference on Harmonisation; Draft Guidance on Q4B Notice NAD-Notice of Availability of Data 2007-12-18T05:00:00Z 2007 12 2007-12-14T05:00:00Z 2008-02-16T04:59:59Z 2009-01-12T16:01:41Z   0 0 090000648042b66c
FDA-2007-D-0200-0002 FDA None FDA-2007-D-0200 International Conference on Harmonisation; Draft Guidance on Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the ICH Regions; Annex on Test for Extractable Volume of Parenteral Preparations General Chapter; Availibilty Notice NAD-Notice of Availability of Data 2007-12-18T05:00:00Z 2007 12 2007-12-14T05:00:00Z 2008-02-16T04:59:59Z 2008-05-28T19:58:35Z   0 0 090000648042abc7
FDA-2005-D-0013-0008 FDA Collection of Platelets by Automated Methods FDA-2005-D-0013 FDA Notice NAD-Notice of Availability of Data 2007-12-18T05:00:00Z 2007 12 2007-12-14T05:00:00Z 2008-12-16T04:59:59Z 2008-04-11T23:46:16Z   0 0 090000648043e53f
FDA-2007-N-0319-0001 FDA None FDA-2007-N-0319 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Health and Diet Survey Notice 30 Day Proposed Information Collection 2007-12-17T05:00:00Z 2007 12 2007-12-13T05:00:00Z 2008-01-15T04:59:59Z 2025-07-18T17:30:47Z E7-24123 0 0 090000648042b7c7
FDA-2007-N-0441-0002 FDA None FDA-2007-N-0441 Agency Emergency Processing Under the Office of Management and Budget Review; Certification to Accompany Drug, Biological Product, and Device Applications or Submissions Notice General Notice 2007-12-12T05:00:00Z 2007 12 2007-12-12T05:00:00Z 2007-12-18T04:59:59Z 2025-08-19T20:24:09Z 07-6023 0 0 090000648042dda4
FDA-2007-N-0272-0002 FDA None FDA-2007-N-0272 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Presubmission Conferences, New Animal Drug Applications and Supporting Regulations and Guidance 152, and Form FDA 356V Notice 30 Day Proposed Information Collection 2007-12-11T05:00:00Z 2007 12 2007-12-11T05:00:00Z 2008-01-11T04:59:59Z 2025-07-23T19:31:13Z E7-23998 0 0 090000648042b3bd
FDA-2007-N-0220-0002 FDA None FDA-2007-N-0220 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance for Industry on Pharmacogenomic Data Submissions; Extension Notice 30 Day Proposed Information Collection 2007-12-11T05:00:00Z 2007 12 2007-12-11T05:00:00Z 2008-01-11T04:59:59Z 2025-08-07T22:57:55Z E7-23996 0 0 090000648042adfb
FDA-2007-N-0383-0003 FDA None FDA-2007-N-0383 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Radioactive Drug Research Committees Notice 30 Day Proposed Information Collection 2007-12-11T05:00:00Z 2007 12 2007-12-10T05:00:00Z 2008-01-11T04:59:59Z 2025-08-11T16:06:25Z E7-23977 0 0 090000648042d750
FDA-2007-C-0044-0002 FDA None FDA-2007-C-0044 DSM Nutritional Products, Inc.; Filing of Color Additive Petition Notice NFL-Notice of Filing 2007-12-11T05:00:00Z 2007 12 2007-12-03T05:00:00Z   2026-01-08T20:19:27Z   0 0 0900006480429647
FDA-2007-N-0080-0001 FDA None FDA-2007-N-0080 Establishment of Fiscal Year 2008 User Fee Rates for Advisory Review of Direct-to-Consumer Television Advertisements for Prescription Drug and Biological Products Notice General Notice 2007-12-11T05:00:00Z 2007 12     2025-08-19T00:31:05Z E7-24000 0 0 09000064804298e2
FDA-2007-N-0266-0001 FDA None FDA-2007-N-0266 Agency Information Collection Activities; Proposed Collection; Comment Request; Reports of Corrections and Removals Notice N-Notice 2007-12-11T05:00:00Z 2007 12 2007-12-11T05:00:00Z 2008-02-12T04:59:59Z 2025-08-18T23:08:07Z E7-23962 0 0 090000648042b37a
FDA-2000-P-0152-0010 FDA Amend Part 133.3 Re: Milk & Nonfat Milk for Use in Standardization FDA-2000-P-0152 FDA Notice NEC-Notice of Extension 2007-12-11T05:00:00Z 2007 12 2007-12-10T05:00:00Z 2008-02-12T04:59:59Z 2008-04-25T01:44:24Z   0 0 09000064804d1371
FDA-2007-N-0087-0001 FDA None FDA-2007-N-0087 Agency Information Collection Activities; Proposed Collection; Comment Request; Mental Models Study of Communicating With Health Care Providers About the Risks and Benefits of Prescription Drug Use for Pregnant and Nursing Women With Chronic Conditions Notice 60 Day Proposed Information Collection 2007-12-11T05:00:00Z 2007 12 2007-12-10T05:00:00Z 2008-02-12T04:59:59Z 2025-09-24T22:10:20Z E7-23976 0 0 0900006480429c98
FDA-2006-N-0239-0007 FDA Index of Legally Marketed Unapproved New Animal Drugs for Minor Species FDA-2006-N-0239 Index of Legally Marketed Unapproved New Animal Drugs for Minor Species; Final Rule Notice Notice of Final Rule 2007-12-06T05:00:00Z 2007 12 2007-12-05T05:00:00Z   2015-12-15T17:50:54Z   0 0 0900006480456f42
FDA-2007-F-0330-0001 FDA None FDA-2007-F-0330 General Mills, Inc.; Filing of Food Additive Petition (FAP 7M4770) Notice NFL-Notice of Filing 2007-12-04T05:00:00Z 2007 12 2007-11-30T05:00:00Z   2026-01-08T19:37:41Z   0 0 090000648042b848
FDA-2007-N-0074-0001 FDA None FDA-2007-N-0074 Number not used Notice NFL-Notice of Filing 2007-12-04T05:00:00Z 2007 12 2007-12-03T05:00:00Z   2008-04-04T00:35:37Z   0 0 090000648042988b
FDA-1995-N-0061-0001 FDA CGMP Certain Requirements for Finished Pharmaceuticals FDA-1995-N-0061 FDA Notice NWL-Notice of Withdrawl 2007-12-04T05:00:00Z 2007 12 2007-12-03T05:00:00Z   2008-05-16T22:33:32Z   0 0 090000648056c4d1
FDA-2007-N-0443-0003 FDA None FDA-2007-N-0443 FDA Notice NFL-Notice of Filing 2007-12-03T05:00:00Z 2007 12 2007-11-30T05:00:00Z   2008-04-04T00:36:42Z   0 0 090000648042ddc0
FDA-2007-N-0323-0002 FDA None FDA-2007-N-0323 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice Regulations for Type A Medicated Articles Notice 30 Day Proposed Information Collection 2007-12-03T05:00:00Z 2007 12 2007-12-03T05:00:00Z 2008-01-03T04:59:59Z 2025-07-29T23:35:15Z E7-23351 0 0 090000648042b7f5
FDA-2007-N-0443-0002 FDA None FDA-2007-N-0443 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Color Additive Certification Requests and Recordkeeplng Notice 30 Day Proposed Information Collection 2007-12-03T05:00:00Z 2007 12 2007-12-03T05:00:00Z 2008-01-03T04:59:59Z 2025-07-28T17:46:21Z E7-23352 0 0 090000648042ddbe
FDA-2005-D-0445-0007 FDA Class II Special Controls: Automated Blood Cell Separator Device Operating by Centrifugal or Filtration Separation Principle, re FDA-2012-N-0115 FDA-2005-D-0445 Guidance for Industry and Food and Drug Administration Staff: Class II Special Controls Guidance Document: Automated Blood Cell Separator Device Operating by Centrifugal or Filtration Separation Principle; Availability Notice Notice of Availability 2007-11-30T05:00:00Z 2007 11 2007-11-30T05:00:00Z   2015-01-20T23:53:18Z   0 0 09000064804505f1
FDA-1976-N-0026-0001 FDA OTC Antitussives-CLOSED FDA-1976-N-0026 Cold, Cough, Allergy, Bronchodilator and Antiasthmatic Drug Products for Over-the-Counter Human Use; Amerndment of Final Monograph for OTC Antitussive Drug Products; Technical Amendment - Notice of Final Rule Notice NFR-Notice of Final Rule 2007-11-30T05:00:00Z 2007 11     2014-10-14T17:01:15Z 72 0 0 090000648051b4ed
FDA-2007-N-0198-0007 FDA None FDA-2007-N-0198 Food Labeling: Use of Symbols to Communicate Nutrition Information, Consideration of Consumer Studies and Nutritional Criteria; Reopening of Comment Period - Notice of Extension Notice NEC-Notice of Extension 2007-11-30T05:00:00Z 2007 11 2007-11-30T05:00:00Z 2008-01-16T04:59:59Z 2009-03-31T19:50:39Z   0 0 090000648042a9d6
FDA-2005-N-0286-0002 FDA Medical Devices; Hematology and Pathology Devices; Reclassification from Class III to Class II of Automated Blood Cell Separator Device Operating by Centrifugal Separation Principle FDA-2005-N-0286 Medical Devices; Hematology and Pathology Devices; Reclassification of Automated Blood Cell Separator Device Operating by Centrifugal Separation Principle Notice Notice of Final Rule 2007-11-30T05:00:00Z 2007 11 2007-11-30T05:00:00Z   2025-09-16T20:42:17Z E7-23285 0 0 0900006480445883
FDA-2007-N-0450-0001 FDA None FDA-2007-N-0450 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution Notice 30 Day Proposed Information Collection 2007-11-30T05:00:00Z 2007 11 2007-11-30T05:00:00Z 2008-01-01T04:59:59Z 2025-08-07T23:39:14Z E7-23275 0 0 090000648042de6d
FDA-2006-F-0056-0004 FDA Safe Use of Cetylpyridinium Chloride as an Antimicrobial Agent in a Pre-chiller or Post-chiller Solution for Application to Raw Poultry Carcasses (FAP 6A4767) FDA-2006-F-0056 Secondary Direct Food Additives Permitted in Food for Human Consumption Notice Notice of Final Rule 2007-11-29T05:00:00Z 2007 11 2007-11-29T05:00:00Z 2008-01-01T04:59:59Z 2026-01-07T18:53:53Z E7-23182 0 0 090000648044416c
FDA-2006-F-0056-0003 FDA Safe Use of Cetylpyridinium Chloride as an Antimicrobial Agent in a Pre-chiller or Post-chiller Solution for Application to Raw Poultry Carcasses (FAP 6A4767) FDA-2006-F-0056 Secondary Direct Food Additives Permitted in Food for Human Consumption Notice Notice of Final Rule 2007-11-29T05:00:00Z 2007 11 2007-11-29T05:00:00Z 2008-01-01T04:59:59Z 2026-01-07T18:50:12Z E7-23182 0 0 090000648044416b
FDA-1978-N-0018-0612 FDA Sunscreen Drug Products -OPEN FDA-1978-N-0018 Sunscreen Drug Products for Over-The-Counter Human Use; Proposed Amendment of Final Monograph; Extension of Comment Period Notice Notice of Extension 2007-11-28T05:00:00Z 2007 11 2007-11-28T05:00:00Z 2007-12-27T04:59:59Z 2019-08-01T16:04:23Z 07-5853 0 0 090000648055c00d
FDA-2007-N-0361-0001 FDA None FDA-2007-N-0361 FDA Notice NRD-Notice of Requesting Data, Info, & Views 2007-11-28T05:00:00Z 2007 11 2007-11-27T05:00:00Z 2008-01-29T04:59:59Z 2008-04-04T00:36:26Z   0 0 090000648042ba35
FDA-2006-P-0006-0004 FDA To permit an ANDA Suitability for Eloxatin (Oxaliplatin for injection) FDA-2006-P-0006 Determination That ELOXATIN (Oxaliplatin for Injection), 50 and 100 Milligrams Per Vial, Sterile Lyophilized Powder for Injection, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice N-Notice 2007-11-27T05:00:00Z 2007 11 2007-11-23T05:00:00Z   2024-11-14T14:37:17Z   0 0 0900006480441444
FDA-2006-P-0069-0004 FDA ANDA for ELOXATIN (oxaliplatin for injection) lyophilized powder for infusion, 50 mg and 100 mg vials FDA-2006-P-0069 Notice of Determination Notice N-Notice 2007-11-27T05:00:00Z 2007 11 2007-11-23T05:00:00Z   2024-11-13T14:49:01Z   0 0 0900006480444464
FDA-2005-P-0371-0002 FDA Nutrient Content Claims for ALA & DHA Omega-3 Fatty Acids FDA-2005-P-0371 FDA Notice NPR-Notice of Proposed Rule-Making 2007-11-27T05:00:00Z 2007 11 2007-11-26T05:00:00Z 2008-02-12T04:59:59Z 2008-04-12T00:10:08Z   0 0 090000648044b3d9
FDA-2006-P-0085-0004 FDA Determine whether Eloxatin (Oxaliplatin for Injection) has been voluntarily withdrawn or withheld from sale for safety or efficacy reasons FDA-2006-P-0085 Notice of Determination Notice N-Notice 2007-11-27T05:00:00Z 2007 11 2007-11-23T05:00:00Z   2024-11-04T19:38:04Z   0 0 090000648044498c
FDA-2007-P-0247-0005 FDA None FDA-2007-P-0247 Determination That ELOXATIN (Oxaliplatin for Injection), 50 and 100 Milligrams Per Vial, Sterile Lyophilized Powder for Injection, Was Not Withdrawn From Saie for Reasons of Safety or Effectiveness Notice N-Notice 2007-11-27T05:00:00Z 2007 11 2007-11-26T05:00:00Z   2025-03-05T16:57:42Z E7-22973 0 0 090000648042b113
FDA-2006-P-0201-0004 FDA Determine whether Eloxatin (Oxaliplatin for Injection) 50 mg and 100 mg sterile lyophilized powder vials (NDA #21-492 has been withdrawn for safety or effectiveness reasons FDA-2006-P-0201 FDA Federal Register announcing the FDA Determination Notice N-Notice 2007-11-27T05:00:00Z 2007 11 2007-11-23T05:00:00Z   2008-06-19T19:57:27Z   0 0 0900006480450f51
FDA-2006-P-0224-0003 FDA Nutrient Content Claim for EPA and DHA omega-3 fatty acids FDA-2006-P-0224 FDA Notice NPR-Notice of Proposed Rule-Making 2007-11-27T05:00:00Z 2007 11 2007-11-26T05:00:00Z 2008-02-12T04:59:59Z 2008-04-11T23:18:48Z   0 0 0900006480456093
FDA-2007-N-0083-0017 FDA None FDA-2007-N-0083 Behind the Counter Availability of Certain Drugs; Public Meeting; Comment Period Clarification Notice NCR-Notice of Correction 2007-11-27T05:00:00Z 2007 11 2007-11-26T05:00:00Z 2007-12-18T04:59:59Z 2008-05-12T05:42:58Z   0 0 0900006480429a98
FDA-2007-D-0132-0001 FDA None FDA-2007-D-0132 Draft Guidance for Industry on Smallpox (Variola) Infection: Developing Drugs for Treatment or Prevention Notice NAD-Notice of Availability of Data 2007-11-23T05:00:00Z 2007 11 2007-11-21T05:00:00Z 2008-01-23T04:59:59Z 2008-08-06T20:00:34Z   0 0 090000648042a2b6
FDA-1999-D-0048-0006 FDA Impurities in New Veterinary Medicinal Products; International Cooperation on Harmonisation of Technical Requirements, VICH GL11 FDA-1999-D-0048 International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products; Revised Guidance for Industry on Impurities in New Veterinary Medicinal Products (Revision); Availability Notice Notice of Data Availability 2007-11-23T05:00:00Z 2007 11 2007-11-21T05:00:00Z 2008-11-22T04:59:59Z 2025-06-10T19:14:10Z E7-22901 0 0 09000064804a6009
FDA-2006-D-0299-0004 FDA Stability Testing of New Veterinary Drug Substances and Medicinal Products (Revision) VICH GL3 (R) (#73) FDA-2006-D-0299 FDA Notice NAD-Notice of Availability of Data 2007-11-23T05:00:00Z 2007 11 2007-11-21T05:00:00Z 2008-11-22T04:59:59Z 2008-04-11T23:06:36Z   0 0 0900006480458fb7
FDA-1999-D-0064-0005 FDA Impurities in New Veterinary Drug Substances FDA-1999-D-0064 International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products; Revised Guidance for Industry on Impurities in New Veterinary Drug Substances (Revision); Availability Notice Notice of Data Availability 2007-11-23T05:00:00Z 2007 11 2007-11-21T05:00:00Z 2008-11-22T04:59:59Z 2025-06-12T19:51:21Z E7-22902 0 0 09000064804a67af
FDA-2004-D-0298-0003 FDA Compliance Policy Guide Sec. 400.210 Radiofrequency Identification Feasibility Studies and Pilot Programs for Drugs, Availability FDA-2004-D-0298 FDA Notice NEC-Notice of Extension 2007-11-23T05:00:00Z 2007 11 2007-11-21T05:00:00Z   2008-04-12T00:35:32Z   0 0 0900006480472d20
FDA-2007-N-0154-0001 FDA None FDA-2007-N-0154 Agency Information Collection Activities; Proposed Collection; Comment Request; Recordkeeping and Records Access Requirements for Food Facilities Notice 60 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11 2007-11-19T05:00:00Z 2008-01-19T04:59:59Z 2025-08-15T21:26:09Z E7-22480 0 0 090000648042a457
FDA-2006-F-0313-0001 FDA Safe Use of Poly (iminoimidocarbonyliminoimidocarbonyliminohexamethylene) Hydrochloride (CAS Reg No. 32289-58-0) as an Antimicrobial Agent in the Manufacture of Food-Contact Paper and Paperboard (FAP 6B4764) FDA-2006-F-0313 ARCH Chemicals, Inc.; Withdrawal of Food Additive Petition FAP 6B4764 Notice Withdrawal 2007-11-20T05:00:00Z 2007 11 2007-11-19T05:00:00Z   2025-12-17T19:50:52Z E7-22536 0 0 090000648045c904
FDA-2007-N-0447-0003 FDA None FDA-2007-N-0447 FDA Notice N-Notice 2007-11-20T05:00:00Z 2007 11 2007-11-16T05:00:00Z   2008-04-04T00:36:45Z   0 0 090000648042de13
FDA-2007-N-0037-0002 FDA None FDA-2007-N-0037 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Animal Drug User Fees and Fee Waivers and Reductions Notice 30 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11 2007-11-19T05:00:00Z 2007-12-20T04:59:59Z 2025-07-23T16:02:33Z E7-22495 0 0 09000064804295db
FDA-2007-N-0217-0002 FDA None FDA-2007-N-0217 Agency Information Collection Activities: Submission for Office of Management and Budget Review; Comment Request; Medical Devices Third-Party Review Under the Food and Drug Administration Modernization Act Notice 30 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11 2007-11-19T05:00:00Z 2007-12-20T04:59:59Z 2025-07-23T18:31:50Z E7-22586 0 0 090000648042add2
FDA-2007-N-0264-0002 FDA None FDA-2007-N-0264 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Voluntary Registration of Cosmetic Product Establishments Notice 30 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11 2007-11-19T05:00:00Z 2007-12-20T04:59:59Z 2025-07-28T17:12:07Z E7-22588 0 0 090000648042b346
FDA-2007-N-0085-0001 FDA None FDA-2007-N-0085 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice Regulations for Medicated Feeds Notice 30 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11     2025-07-29T23:04:30Z   0 0 0900006480429c7e
FDA-2007-N-0267-0001 FDA None FDA-2007-N-0267 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Animal Drug User Fee Cover Sheet, FDA Form 3546 Notice 30 Day Proposed Information Collection 2007-11-20T05:00:00Z 2007 11 2007-11-20T05:00:00Z 2007-12-21T04:59:59Z 2025-07-23T16:52:02Z E7-22649 0 0 090000648042b383
FDA-2007-N-0039-0001 FDA None FDA-2007-N-0039 Agency Emergency Processing Under Office of Management and Budget Review; Orphan Drug Products; Common European Medicines Evaluation Agency/Food and Drug Administration Application Form for Orphan Medicinal Product Designation Notice General Notice 2007-11-09T05:00:00Z 2007 11 2007-11-09T05:00:00Z 2007-11-20T04:59:59Z 2025-08-15T18:39:29Z E7-21988 0 0 09000064804295f2
FDA-2007-M-0389-0001 FDA None FDA-2007-M-0389 Medical Devices Regulated by the Center for Biologics Evaluation and Research; Availability of Summaries of Safety and Effectiveness Data for Premarket Approval Applications Notice Notice of Data Availability 2007-11-09T05:00:00Z 2007 11 2007-11-09T05:00:00Z   2026-01-13T02:23:08Z E7-21986 0 0 090000648042d7c1
FDA-2007-N-0428-0001 FDA None FDA-2007-N-0428 Agency Information Collection Activities; Proposed Collection; Comment Request; Application for Participation in the Medical Device Fellowship Program Notice 60 Day Proposed Information Collection 2007-11-09T05:00:00Z 2007 11 2007-11-09T05:00:00Z 2008-01-09T04:59:59Z 2025-08-15T16:40:31Z E7-21971 0 0 090000648042dc01
FDA-2007-D-0133-0001 FDA None FDA-2007-D-0133 See FDA-2007-D-0133-0003 Notice   2007-11-09T00:00:00Z 2007 11     2008-05-28T00:54:44Z   0 1 090000648042a2c0
FDA-2007-N-0314-0010 FDA None FDA-2007-N-0314 Use of Ozone-Depleting Substances; Removal of Essential-Use Designation (Epinephrine) - Notice of Public Meeting and Extension of Comment Period Notice NEC-Notice of Extension 2007-11-08T05:00:00Z 2007 11 2007-11-08T05:00:00Z 2007-12-20T04:59:59Z 2008-11-19T13:48:39Z   0 0 090000648042b762
FDA-2007-N-0073-0001 FDA None FDA-2007-N-0073 Lederle Laboratories et al.; Withdrawal of Approval of 73 New Drug Applications and 62 Abbreviated New Drug Applications Notice Withdrawal 2007-11-08T05:00:00Z 2007 11     2025-09-16T21:26:14Z E7-21886 0 0 0900006480429885
FDA-2007-N-0197-0001 FDA None FDA-2007-N-0197 Adolescent Over-the-Counter Drug Product Use; Public Workshop Notice Meeting 2007-11-05T04:00:00Z 2007 11 2007-11-05T05:00:00Z 2008-02-01T04:59:59Z 2025-09-16T18:54:47Z E7-21713 0 0 090000648042a932
FDA-2002-D-0094-0003 FDA Disclosure of Conflicts of Interest for Special Government Employees FDA-2002-D-0094 Draft Guidance for the Public, Food and Drug Administration Advisory Committee Members, and Food and Drug Administration Staff: Public Availability of Advisory Committee Members Financial Interest Information and Waivers; Availability Notice NAD-Notice of Availability of Data 2007-10-31T04:00:00Z 2007 10 2007-10-31T04:00:00Z 2008-01-01T04:59:59Z 2010-08-06T23:52:22Z   0 0 090000648048e4a5
FDA-2007-D-0375-0001 FDA None FDA-2007-D-0375 FDA Notice NAD-Notice of Availability of Data 2007-10-30T04:00:00Z 2007 10 2007-10-29T04:00:00Z 2008-01-29T04:59:59Z 2008-07-21T19:57:16Z   0 0 090000648042c89d
FDA-2007-F-0046-0002 FDA None FDA-2007-F-0046 Biomin GmbH; Filing of Food Additive Petition Notice Notice of Filing 2007-10-30T04:00:00Z 2007 10 2007-10-29T04:00:00Z 2008-01-01T04:59:59Z 2026-01-03T00:16:28Z   0 0 090000648042965e
FDA-2005-D-0211-0050 FDA Guidance for Industry: Considerations for Plasmid DNA Vaccines for Infectious Disease Indications FDA-2005-D-0211 FDA Notice NAD-Notice of Availability of Data 2007-10-29T04:00:00Z 2007 10 2007-10-26T04:00:00Z   2008-04-11T23:46:52Z   0 0 0900006480441500
FDA-2007-D-0069-0001 FDA None FDA-2007-D-0069 FDA Notice NAD-Notice of Availability of Data 2007-10-29T04:00:00Z 2007 10 2007-10-26T04:00:00Z 2008-01-29T04:59:59Z 2008-04-04T00:34:03Z   0 0 0900006480429834
FDA-2007-D-0367-0001 FDA None FDA-2007-D-0367 Draft Guidance for Industry and Food and Drug Administration Staff; Impact Resistant Lenses: Questions and Answers; Availability Notice NAD-Notice of Availability of Data 2007-10-26T04:00:00Z 2007 10 2007-10-26T04:00:00Z 2008-01-25T04:59:59Z 2008-05-19T23:59:38Z   0 0 090000648042bb4e
FDA-2003-N-0441-0002 FDA Exocrine Pancreatic Insufficiency Drug Products FDA-2003-N-0441 Exocrine Pancreatic Insufficiency Drug Products; Extension to Obtain Marketing Approval Notice General Notice 2007-10-26T04:00:00Z 2007 10 2007-10-26T04:00:00Z   2025-03-05T19:50:55Z E7-21082 0 0 09000064804a245c
FDA-2007-D-0309-0001 FDA None FDA-2007-D-0309 Drug-Induced Liver Injury; Premarketing Clinical Evaluation; Draft Guidance Notice NAD-Notice of Availability of Data 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z 2007-12-25T04:59:59Z 2008-08-27T17:27:07Z 72FR60681 0 0 090000648042b6c1
FDA-2006-N-0176-0003 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Continuous Marketing Applications: Pilot 2 - Scientific Feedback and Interactions During Development of Fast Track Products Under the Prescription Drug User Fee Act FDA-2006-N-0176 Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Guidance for Industry on Continuous Marketing Applications: Pilot- Scientific Feedback and Interactions During Development of Fast Track Products Under the Prescription Drug User Fee Act Notice Notice of Approval 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z   2025-06-20T17:24:04Z E7-21056 0 0 0900006480450b60
FDA-2007-N-0446-0001 FDA None FDA-2007-N-0446 User Fee Program for Advisory Review of Direct-to-Consumer Television Advertisements for Prescription Drug and Biological Products; Request for Notification of Participation and Number of Advertisements for Review Notice General Notice 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z 2007-11-27T04:59:59Z 2025-08-14T18:54:22Z 07-5282 0 0 090000648042de03
FDA-2007-D-0369-0002 FDA None FDA-2007-D-0369 Publication of Guidances for Industry Describing Product-Specific Bioequivalence Recommendations Notice NAD-Notice of Availability of Data 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z 2007-12-25T04:59:59Z 2008-05-20T19:33:47Z   0 0 090000648042bb9e
FDA-1999-N-0114-0007 FDA Current Good Manufacturing Practice for Blood & Blood Components; Notification of Consignees & Transfusion Recipients Receiving Blood & Blood Components at Increased Risk of Transmitting Hepatitis C Virus Infection ("Lookback") FDA-1999-N-0114 Notice of Approval re Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; CGMP for Blood and Blood Components; Notification of Consignees and Transfusion Recipients Receiving Blood and Blood Components at Increased Risk of Transmitting HCV Infection ("Lookback") Notice Notice of Approval 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z   2024-10-03T21:46:36Z 72FR48766 0 0 09000064804ae8e8
FDA-2007-D-0076-0001 FDA None FDA-2007-D-0076 FDA Notice NAD-Notice of Availability of Data 2007-10-25T04:00:00Z 2007 10 2007-10-25T04:00:00Z 2008-01-24T04:59:59Z 2008-04-04T00:34:05Z   0 0 090000648042989f
FDA-2006-N-0111-0004 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Experimental Evaluation of Variations in Content and Format of the Brief Summary in Direct-to-Consumer (DTC) Print Advertisements for Prescription Drugs FDA-2006-N-0111 Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Experimental Evaluation of Variations in Content and Format of the Brief Summary in Direct-to-Consumer Print Advertisements for Prescription Drugs Notice Notice of Approval 2007-10-24T04:00:00Z 2007 10 2007-10-22T04:00:00Z   2025-06-16T16:28:20Z E7-20756 0 0 09000064804500c3
FDA-2007-D-0258-0001 FDA None FDA-2007-D-0258 FDA Notice NAD-Notice of Availability of Data 2007-10-24T04:00:00Z 2007 10 2007-10-18T04:00:00Z   2008-04-04T00:34:20Z   0 0 090000648042b1ca
FDA-2007-N-0363-0015 FDA None FDA-2007-N-0363 FDA Notice N-Notice 2007-10-24T04:00:00Z 2007 10 2007-10-19T04:00:00Z 2007-12-07T04:59:59Z 2008-04-04T00:36:28Z   0 0 090000648042bacf
FDA-2007-P-0108-0004 FDA None FDA-2007-P-0108 Nonprescription Drugs Advisory Committee; Notice of Meeting Notice Meeting 2007-10-24T04:00:00Z 2007 10 2007-10-24T04:00:00Z 2007-12-31T04:59:59Z 2025-07-09T23:09:12Z 07-5249 0 0 0900006480429e46
FDA-2006-D-0168-0010 FDA Guidance for Industry: Guide to Minimize Food Safety Hazards for Fresh-cut Fruits and Vegetables FDA-2006-D-0168 FDA Notice NAL-Notice of Approval 2007-10-19T04:00:00Z 2007 10 2007-10-19T04:00:00Z   2008-04-11T23:03:24Z   0 0 09000064804508f8
FDA-2007-D-0028-0001 FDA None FDA-2007-D-0028 FDA Notice NAD-Notice of Availability of Data 2007-10-19T04:00:00Z 2007 10 2007-10-19T04:00:00Z   2008-04-04T00:34:00Z   0 0 09000064804294a1
FDA-2007-N-0082-0002 FDA None FDA-2007-N-0082 Revision of the Requirements for Live Vaccine Processing Notice Notice of Final Rule 2007-10-19T04:00:00Z 2007 10 2007-10-17T04:00:00Z 2008-01-03T04:59:59Z 2025-07-29T17:31:25Z E7-20610 0 0 0900006480429902
FDA-2000-N-0143-0002 FDA Proposed Revision of Postmarketing Reporting Requirements FDA-2000-N-0143 Applications for Food and Drug Administration Application Approval to Market a New Drug; Revision of Postmarketing Reporting Requirements Notice Notice of Final Rule 2007-10-19T04:00:00Z 2007 10 2007-10-18T04:00:00Z   2025-06-13T00:26:00Z E7-20510 0 0 09000064804d0dec
FDA-2007-N-0362-0001 FDA None FDA-2007-N-0362 FDA Notice N-Notice 2007-10-19T04:00:00Z 2007 10 2007-10-19T04:00:00Z   2008-04-04T00:36:26Z   0 0 090000648042ba40
FDA-2007-N-0082-0001 FDA None FDA-2007-N-0082 Revision of the Requirements for Live Vaccine Processing; Companion to Direct Final Rule Notice NPR-Notice of Proposed Rule-Making 2007-10-19T04:00:00Z 2007 10 2007-10-18T04:00:00Z 2008-01-03T04:59:59Z 2025-07-30T09:00:20Z E7-20609 0 0 09000064804298fe
FDA-2007-N-0216-0002 FDA None FDA-2007-N-0216 FDA Notice N-Notice 2007-10-19T04:00:00Z 2007 10 2007-10-19T04:00:00Z 2008-10-21T03:59:59Z 2008-04-04T00:36:03Z   0 0 090000648042adc3
FDA-2000-D-0221-0007 FDA Guidance for Industry: Special Protocol Assessment FDA-2000-D-0221 FDA Notice NAL-Notice of Approval 2007-10-19T04:00:00Z 2007 10 2007-10-17T04:00:00Z   2008-04-25T01:14:34Z   0 0 09000064804d5177
FDA-2007-D-0420-0001 FDA None FDA-2007-D-0420 Draft Guidance for Industry on the Use of Mechanical Calibration of Dissolution Apparatus 1 and 2 Current Good Manufacturing Practice; Availability Notice NAD-Notice of Availability of Data 2007-10-19T04:00:00Z 2007 10 2007-10-19T04:00:00Z 2007-12-19T04:59:59Z 2008-04-19T00:59:52Z   0 0 090000648042dab4
FDA-2007-N-0388-0004 FDA None FDA-2007-N-0388 Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Toll-Free Number for Consumer Reporting of Drug Product Side Effects: Comprehension Notice Notice of Approval 2007-10-17T04:00:00Z 2007 10     2025-07-01T23:39:15Z E7-20075 0 0 090000648042d7b8
FDA-2001-D-0045-0002 FDA Guidance for Industry - Yellow Corn & Dry-Milled FDA-2001-D-0045 FDA Notice N-Notice 2007-10-17T04:00:00Z 2007 10 2007-10-17T04:00:00Z 2007-12-18T04:59:59Z 2008-04-25T01:57:24Z   0 0 09000064804b7519
FDA-2007-N-0040-0002 FDA None FDA-2007-N-0040 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Institutional Review Boards Notice 30 Day Proposed Information Collection 2007-10-17T04:00:00Z 2007 10 2007-10-11T04:00:00Z 2007-11-14T04:59:59Z 2025-07-23T23:25:29Z E7-20063 0 0 0900006480429604

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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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