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

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797 rows where agency_id = "FDA", document_type = "Notice" and posted_year = 2010 sorted by posted_date descending

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posted_year 1

  • 2010 · 797 ✖

document_type 1

  • Notice · 797 ✖

agency_id 1

  • FDA · 797 ✖
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2010-N-0118-0005 FDA FDA-2010-N-0118 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Imported Food under 2002 Public Health Security and Bioterrorism Preparedness and Response Act of 2002 Notice N-Notice 2010-12-30T05:00:00Z 2010 12 2010-12-30T05:00:00Z   2010-12-30T14:44:54Z 2010-32946 0 0 0900006480bc26ef
FDA-2010-N-0356-0004 FDA FDA-2010-N-0356 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Designated New Animal Drugs for Minor Use and Minor Species Notice N-Notice 2010-12-30T05:00:00Z 2010 12 2010-12-30T05:00:00Z   2010-12-30T14:39:28Z 2010-32948 0 0 0900006480bc26eb
FDA-2010-N-0001-0163 FDA FDA-2010-N-0001 Meetings: Pulmonary-Allergy Drugs Advisory Committee Notice NM-Notice of Meeting 2010-12-29T05:00:00Z 2010 12 2010-12-29T05:00:00Z   2010-12-29T15:23:00Z 2010-32735 0 0 0900006480bc1b9a
FDA-2010-N-0640-0001 FDA FDA-2010-N-0640 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Data To Support Food and Nutrition Product Communications, as Used by Food and Drug Administration Notice N-Notice 2010-12-29T05:00:00Z 2010 12 2010-12-29T05:00:00Z 2011-03-01T04:59:59Z 2010-12-29T15:29:12Z 2010-32739 0 0 0900006480bc1bc0
FDA-2010-N-0198-0003 FDA FDA-2010-N-0198 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Premarket Notification Notice N-Notice 2010-12-28T05:00:00Z 2010 12 2010-12-28T05:00:00Z   2010-12-28T16:44:38Z 2010-32508 0 0 0900006480bc11ca
FDA-2010-P-0326-0003 FDA FDA-2010-P-0326 Determination that Products Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness: TRANDATE (Labetalol Hydrochloride) Tablets, 300 Milligrams and 400 Milligrams Notice N-Notice 2010-12-28T05:00:00Z 2010 12 2010-12-28T05:00:00Z   2010-12-28T16:37:57Z 2010-32507 0 0 0900006480bc11ac
FDA-2010-N-0001-0161 FDA FDA-2010-N-0001 Meetings: Anesthetic and Life Support Drugs Advisory Committee Notice NM-Notice of Meeting 2010-12-28T05:00:00Z 2010 12 2010-12-28T05:00:00Z   2010-12-28T16:11:53Z 2010-32591 0 0 0900006480bc0c47
FDA-2010-N-0001-0162 FDA FDA-2010-N-0001 Request for Nominations: Voting and Non-Voting Members of Public Advisory Committees or Panels Notice N-Notice 2010-12-28T05:00:00Z 2010 12 2010-12-28T05:00:00Z   2010-12-28T16:28:32Z 2010-32624 0 0 0900006480bc1153
FDA-2010-N-0447-0003 FDA FDA-2010-N-0447 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Third Party Review Program Under the Food and Drug Administration Modernization Act Notice N-Notice 2010-12-28T05:00:00Z 2010 12 2010-12-28T05:00:00Z   2011-03-14T20:37:01Z 2010-32603 0 0 0900006480bc0c82
FDA-2010-N-0001-0160 FDA FDA-2010-N-0001 Circulatory System Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting Notice NM-Notice of Meeting 2010-12-27T05:00:00Z 2010 12 2010-12-27T05:00:00Z   2010-12-27T14:48:01Z 2010-32367 0 0 0900006480bc03c3
FDA-2010-N-0001-0159 FDA FDA-2010-N-0001 Oncologic Drugs Advisory Committee; Cancellation Notice N-Notice 2010-12-27T05:00:00Z 2010 12 2010-12-27T05:00:00Z   2010-12-27T14:44:55Z 2010-32413 0 0 0900006480bc0306
FDA-2010-D-0575-0001 FDA FDA-2010-D-0575 Draft Compliance Policy Guide Sec. 510.800 Beverages, Serving Size Labeling; Availability Notice NAD-Notice of Availability of Data 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z 2011-02-23T04:59:59Z 2010-12-23T14:41:09Z 2010-32249 0 0 0900006480bbe9be
FDA-2010-N-0266-0007 FDA FDA-2010-N-0266 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Study of Clinical Efficacy Information in Professional Labeling, etc.; Correction Notice NCR-Notice of Correction 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z   2010-12-23T15:27:48Z 2010-32278 0 0 0900006480bbea66
FDA-2010-N-0631-0001 FDA FDA-2010-N-0631 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance for Industry on Updating Labeling for Susceptibility Test Information in Systemic Antibacterial Drug Products, etc. Notice N-Notice 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z 2011-02-23T04:59:59Z 2010-12-23T15:30:54Z 2010-32276 0 0 0900006480bbea69
FDA-2009-D-0466-0008 FDA FDA-2009-D-0466 Compliance Policy Guide; Dairy Products; Availability: Microbial Contaminants and Alkaline Phosphatase Activity Notice NAD-Notice of Availability of Data 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z   2024-11-07T22:30:06Z 2010-32232 1 0 0900006480bbe9e4
FDA-2010-N-0074-0003 FDA FDA-2010-N-0074 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments, etc. Notice N-Notice 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z   2010-12-23T14:16:46Z 2010-32277 0 0 0900006480bbe9b2
FDA-2010-N-0368-0007 FDA FDA-2010-N-0368 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Pet Event Tracking Network -- State, Federal Cooperation to Prevent Spread of Pet Food Related Diseases Notice N-Notice 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z 2011-01-25T04:59:59Z 2010-12-23T14:34:11Z 2010-32275 0 0 0900006480bbe9b3
FDA-2004-D-0298-0005 FDA Compliance Policy Guide Sec. 400.210 Radiofrequency Identification Feasibility Studies and Pilot Programs for Drugs, Availability FDA-2004-D-0298 Compliance Policy Guides: Radiofrequency Identification Feasibility Studies and Pilot Programs for Drugs Notice NEC-Notice of Extension 2010-12-23T05:00:00Z 2010 12 2010-12-23T05:00:00Z   2024-11-07T22:30:10Z 2010-32274 1 0 0900006480bbea44
FDA-2010-N-0001-0158 FDA FDA-2010-N-0001 Meetings: Advisory Committees; Tentative Schedule for 2011 Notice N-Notice 2010-12-21T05:00:00Z 2010 12 2010-12-21T05:00:00Z   2010-12-21T14:54:16Z 2010-31961 0 0 0900006480bbcc5e
FDA-2010-N-0626-0001 FDA FDA-2010-N-0626 Abbott Laboratories, Inc.; Withdrawal of Approval of a New Drug Application for MERIDIA Notice Withdrawal 2010-12-21T05:00:00Z 2010 12     2018-02-26T16:00:33Z 2010-31986 0 0 0900006480bbcc3f
FDA-2010-E-0042-0005 FDA FDA-2010-E-0042 Regulatory Review Periods for Purposes of Patent Extensions; Determinations: LIVALO Notice N-Notice 2010-12-20T05:00:00Z 2010 12 2010-12-20T05:00:00Z 2011-02-19T04:59:59Z 2010-12-20T16:01:56Z 2010-31847 0 0 0900006480bba8e1
FDA-2010-N-0420-0004 FDA FDA-2010-N-0420 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Testing Communications on FDA-Regulated Products Used in Animals Notice N-Notice 2010-12-20T05:00:00Z 2010 12 2010-12-20T05:00:00Z 2011-01-20T04:59:59Z 2010-12-20T15:38:33Z 2010-31891 0 0 0900006480bba849
FDA-2010-N-0528-0001 FDA FDA-2010-N-0528 Unapproved Animal Drugs Notice N-Notice 2010-12-20T05:00:00Z 2010 12 2010-12-20T05:00:00Z 2011-02-19T04:59:59Z 2010-12-20T15:22:13Z 2010-31889 0 0 0900006480bba831
FDA-2010-E-0030-0005 FDA FDA-2010-E-0030 Regulatory Review Periods for Purposes of Patent Extensions; Determinations: FOLOTYN Notice N-Notice 2010-12-20T05:00:00Z 2010 12 2010-12-20T05:00:00Z 2011-02-19T04:59:59Z 2010-12-20T15:54:26Z 2010-31846 0 0 0900006480bba892
FDA-2010-N-0001-0157 FDA FDA-2010-N-0001 Meetings: Defense Advanced Research Projects Agency and Food and Drug Administration Expanding in Vivo Biomarker Detection Devices Workshop Notice NM-Notice of Meeting 2010-12-20T05:00:00Z 2010 12 2010-12-20T05:00:00Z   2010-12-20T15:47:37Z 2010-31811 0 0 0900006480bba880
FDA-2010-N-0627-0001 FDA FDA-2010-N-0627 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Application for Food and Drug Administration Approval to Market New Drug Notice N-Notice 2010-12-17T05:00:00Z 2010 12 2010-12-17T05:00:00Z 2011-02-16T04:59:59Z 2010-12-17T14:36:03Z 2010-31693 0 0 0900006480bb91f0
FDA-2010-N-0235-0001 FDA FDA-2010-N-0235 Debarment Orders: Ehigiator O. Akhigbe Notice NFR-Notice of Final Rule 2010-12-17T05:00:00Z 2010 12 2010-12-17T05:00:00Z   2010-12-17T14:31:06Z 2010-31776 0 0 0900006480bb919d
FDA-2010-D-0605-0001 FDA FDA-2010-D-0605 Small Entity Compliance Guides; Availability, etc.: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements Notice NAD-Notice of Availability of Data 2010-12-16T05:00:00Z 2010 12 2010-12-16T05:00:00Z   2024-11-12T05:00:25Z 2010-31613 1 0 0900006480bb8272
FDA-2001-E-0027-0020 FDA Angiomax, Patent Term Extension Application, No. 5,196,404 FDA-2001-E-0027 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: ANGIOMAX Notice N-Notice 2010-12-16T05:00:00Z 2010 12 2010-12-16T05:00:00Z   2024-11-12T05:00:23Z 2010-31583 1 0 0900006480bb825a
FDA-2010-D-0616-0001 FDA FDA-2010-D-0616 Draft Guidance for Industry; Availability: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination Notice NAD-Notice of Availability of Data 2010-12-15T05:00:00Z 2010 12 2010-12-15T05:00:00Z 2011-02-15T04:59:59Z 2010-12-15T22:26:14Z 2010-31426 0 0 0900006480bb7048
FDA-2010-N-0184-0007 FDA FDA-2010-N-0184 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Experimental Study of Patient Information Prototypes Notice NAD-Notice of Availability of Data 2010-12-15T05:00:00Z 2010 12 2010-12-15T05:00:00Z 2011-01-15T04:59:59Z 2010-12-15T21:58:54Z 2010-31388 0 0 0900006480bb7010
FDA-2010-N-0623-0001 FDA FDA-2010-N-0623 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Voluntary Cosmetic Registration Program Notice N-Notice 2010-12-15T05:00:00Z 2010 12 2010-12-15T05:00:00Z 2011-02-15T04:59:59Z 2010-12-15T22:04:45Z 2010-31386 0 0 0900006480bb7013
FDA-2009-D-0008-0009 FDA FDA-2009-D-0008 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance for Industry on Citizen Petitions and Petitions for Stay of Action Subject to Section 505(q) of Federal Food, Drug, and Cosmetic Act Notice N-Notice 2010-12-15T05:00:00Z 2010 12     2010-12-15T22:16:59Z 2010-31380 0 0 0900006480bb70ec
FDA-2010-N-0380-0002 FDA FDA-2010-N-0380 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Generic Food and Drug Administration Rapid Response Surveys Notice N-Notice 2010-12-15T05:00:00Z 2010 12 2010-12-15T05:00:00Z 2011-01-15T04:59:59Z 2010-12-15T21:54:50Z 2010-31381 0 0 0900006480bb6f22
FDA-2009-N-0360-0003 FDA FDA-2009-N-0360 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Public Health Notification Readership Survey Notice N-Notice 2010-12-15T05:00:00Z 2010 12     2010-12-15T22:09:18Z 2010-31387 0 0 0900006480bb7067
FDA-2010-N-0418-0003 FDA FDA-2010-N-0418 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Institutional Review Boards Notice N-Notice 2010-12-15T05:00:00Z 2010 12     2010-12-15T22:13:12Z 2010-31389 0 0 0900006480bb70a6
FDA-2010-E-0038-0005 FDA FDA-2010-E-0038 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: SAMSCA Notice N-Notice 2010-12-14T05:00:00Z 2010 12 2010-12-14T05:00:00Z   2010-12-14T20:35:51Z 2010-31298 0 0 0900006480bb6397
FDA-2009-E-0014-0006 FDA FDA-2009-E-0014 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: FREESTYLE NAVIGATOR Notice N-Notice 2010-12-14T05:00:00Z 2010 12 2010-12-14T05:00:00Z   2010-12-14T20:43:14Z 2010-31240 0 0 0900006480bb5eeb
FDA-2010-E-0024-0005 FDA FDA-2010-E-0024 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: VIBATIV Notice N-Notice 2010-12-14T05:00:00Z 2010 12 2010-12-14T05:00:00Z   2010-12-14T19:45:10Z 2010-31250 0 0 0900006480bb6337
FDA-2010-E-0022-0005 FDA FDA-2010-E-0022 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: VIBATIV Notice N-Notice 2010-12-14T05:00:00Z 2010 12 2010-12-14T05:00:00Z   2010-12-14T19:17:04Z 2010-31250 0 0 0900006480bb5ecf
FDA-2010-N-0618-0001 FDA FDA-2010-N-0618 Statements of Organization, Functions and Delegations of Authority Notice N-Notice 2010-12-14T05:00:00Z 2010 12     2010-12-15T22:21:20Z 2010-31383 0 0 0900006480bb70c2
FDA-2010-E-0037-0005 FDA FDA-2010-E-0037 Determinations of Regulatory Review Periods for Purposes of Patent Extensions: SAMSCA Notice N-Notice 2010-12-14T05:00:00Z 2010 12 2010-12-14T05:00:00Z   2010-12-14T16:49:55Z 2010-31298 0 0 0900006480bb5ebd
FDA-2010-N-0622-0001 FDA FDA-2010-N-0622 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Color Additive Certification Requests and Recordkeeping Notice 60 Day Proposed Information Collection 2010-12-13T05:00:00Z 2010 12 2010-12-13T05:00:00Z 2011-02-12T04:59:59Z 2017-03-17T14:13:33Z 2010-31195 0 0 0900006480bb4ff1
FDA-1976-N-0111-0001 FDA Food Additives and Animal Products, Recodification FDA-1976-N-0111 Food and Drug Administration, Department of Health, Education, and Welfare; Recodification Editorial and Technical Amendments Notice N-Notice 2010-12-13T05:00:00Z 2010 12 2010-12-13T05:00:00Z   2010-12-13T23:14:26Z   0 0 090000648051dacf
FDA-2010-N-0389-0017 FDA FDA-2010-N-0389 Meetings: Medical Device User Fee Program; Request for Notification of Patientand Consumer Advocacy Group Intentions to Participate Notice N-Notice 2010-12-13T05:00:00Z 2010 12 2010-12-13T05:00:00Z   2010-12-13T15:25:18Z 2010-31160 0 0 0900006480bb4fc1
FDA-2010-E-0040-0006 FDA FDA-2010-E-0040 Deteermination of Regulatory Review Period for Purposes of Patent Extension; MULTAQ Notice N-Notice 2010-12-10T05:00:00Z 2010 12 2010-12-10T05:00:00Z   2010-12-10T16:25:59Z   0 0 0900006480bb3d90
FDA-2010-N-0001-0156 FDA FDA-2010-N-0001 Tobacco Products Scientific Advisory Committee; Notice of Meeting Notice GDL-Guidance 2010-12-10T05:00:00Z 2010 12 2010-12-10T05:00:00Z   2010-12-10T16:30:50Z 2010-31066 0 0 0900006480bb392a
FDA-2005-D-0072-0005 FDA Draft Guidance on the Open Public Hearing, FDA Advisory Committee Meetings FDA-2005-D-0072 Guidance for Public, FDA Advisory Committee Members, and FDA Staff; Availability: The Open Public Hearing at FDA Advisory Committee Meetings;Availability Notice NAD-Notice of Availability of Data 2010-12-10T05:00:00Z 2010 12 2010-12-10T05:00:00Z   2024-11-07T22:28:26Z 2010-31022 1 0 0900006480bb387e
FDA-2009-E-0510-0012 FDA FDA-2009-E-0510 Determination of Regulatory Review Period for Purposes of Patent Extension: COARTEM Notice N-Notice 2010-12-10T05:00:00Z 2010 12 2010-12-10T05:00:00Z   2024-11-07T22:28:12Z 2010-31074 1 0 0900006480bb3967
FDA-2010-E-0039-0006 FDA FDA-2010-E-0039 Determination of Regulatory Review Period for Purposes of Patent Extension: MULTAQ Notice N-Notice 2010-12-10T05:00:00Z 2010 12 2010-12-10T05:00:00Z   2010-12-10T16:20:27Z 2010-31064 0 0 0900006480bb389f
FDA-2010-E-0021-0005 FDA FDA-2010-E-0021 Determinations of Regulatory Review Periods for Purposes of Patent Extension; SABRIL Notice N-Notice 2010-12-09T05:00:00Z 2010 12 2010-12-09T05:00:00Z   2024-11-07T22:27:57Z 2010-30995 1 0 0900006480bb2d85
FDA-2010-E-0044-0005 FDA FDA-2010-E-0044 Determinations of Regulatory Review Periods for Purposes of Patent Extension; BEPREVE Notice N-Notice 2010-12-09T05:00:00Z 2010 12 2010-12-09T05:00:00Z   2024-11-07T22:28:14Z 2010-30991 1 0 0900006480bb2846
FDA-2010-E-0047-0003 FDA FDA-2010-E-0047 Determination of Regulatory Review Period for Purposes of Patent Extension; ILARIS Notice N-Notice 2010-12-09T05:00:00Z 2010 12 2010-12-09T05:00:00Z   2024-11-07T22:27:57Z 2010-30992 1 0 0900006480bb2d66
FDA-2010-P-0177-0004 FDA FDA-2010-P-0177 Determination That AUGMENTIN ‘125’ (Amoxicillin; Clavulanate Potassium) Chewable Tablet and Six Other AUGMENTIN (Amoxicillin; Clavulanate Potassium) Drug Products Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness Notice N-Notice 2010-12-08T05:00:00Z 2010 12 2010-12-08T05:00:00Z   2010-12-08T16:13:47Z 2010-30622 0 0 0900006480bb20d9
FDA-2010-N-0602-0001 FDA FDA-2010-N-0602 Biologies Price Competition and Innovation Act of 2009;Meetings: User Fee Program for Biosimilar and Interchangeable Biological Product Applications; Request for Notification of Stakeholer Intention to Participate Notice N-Notice 2010-12-08T05:00:00Z 2010 12 2010-12-08T05:00:00Z 2011-01-11T04:59:59Z 2010-12-08T16:09:30Z 2010-30713 0 0 0900006480bb1e4f
FDA-2010-N-0088-0003 FDA FDA-2010-N-0088 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Electronic Products; General Requirements Notice NAL-Notice of Approval 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-08T14:17:25Z 2010-30555 0 0 0900006480bb0cf7
FDA-2010-N-0568-0006 FDA FDA-2010-N-0568 Required Warnings for Cigarette Packages and Advertisements; Research Report Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z 2011-01-12T04:59:59Z 2011-06-11T16:29:00Z 2010-30685 0 0 0900006480bb0be7
FDA-2010-P-0172-0005 FDA FDA-2010-P-0172 Determinations that Drug Products Not Withdrawn from Sale for Reasons of Safety or Effectiveness: AUGMENTIN 125 (Amoxicillin; Clavulanate Potassium) Chewable Tablet and Six Other AUGMENTIN (Amoxicillin; Clavulanate Potassium) Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-07T17:42:31Z 2010-30622 0 0 0900006480bb0c74
FDA-2010-N-0551-0001 FDA FDA-2010-N-0551 Compliance Policy Guides; Withdrawals: Laser(s) as Medical Devices for Facelift, Wrinkle Removal, Acupuncture, Auricular Stimulation, etc. Notice NWL-Notice of Withdrawl 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-07T16:06:30Z 2010-30679 0 0 0900006480bb0c03
FDA-2010-N-0316-0002 FDA FDA-2010-N-0316 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Adverse Event Pilot Program for Medical Products Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z 2011-01-07T04:59:59Z 2010-12-07T16:43:53Z 2010-30583 0 0 0900006480bb0c2a
FDA-2010-N-0550-0001 FDA FDA-2010-N-0550 Withdrawals Of Guidance: Compliance Policy Guide Sec. 390.500 Definition of High-Voltage Vacuum Switch Notice NWL-Notice of Withdrawl 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-08T13:59:45Z 2010-30677 0 0 0900006480bb0caf
FDA-2010-N-0001-0154 FDA FDA-2010-N-0001 Meetings: Third Annual Sentinel Initiative; Public Workshop Notice NM-Notice of Meeting 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-08T14:06:32Z 2010-30562 0 0 0900006480bb0c93
FDA-2010-P-0275-0003 FDA FDA-2010-P-0275 Determinations that Product Withdrawal From Sale Was Not for Reasons of Safety or Effectiveness: GLEEVEC (Imatinib Mesylate) Capsules, 50 Milligrams and 100 Milligrams Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-07T15:24:43Z 2010-30570 0 0 0900006480bb0be6
FDA-2004-N-0056-0012 FDA Annual Guidance Agenda FDA-2004-N-0056 Annual Guidance Agenda - Notice Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2011-01-19T13:30:11Z 2010-30623 0 0 0900006480bb0c04
FDA-2010-N-0606-0001 FDA FDA-2010-N-0606 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Additional Listing Information for Medical Device Registration and Listing Notice N-Notice 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z 2011-02-08T04:59:59Z 2010-12-08T14:31:55Z 2010-30582 0 0 0900006480bb0c5c
FDA-2010-N-0083-0004 FDA FDA-2010-N-0083 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Substances Prohibited From Use in Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed Notice NAL-Notice of Approval 2010-12-07T05:00:00Z 2010 12 2010-12-07T05:00:00Z   2010-12-08T14:20:57Z 2010-30556 0 0 0900006480bb0c4c
FDA-2010-N-0001-0152 FDA FDA-2010-N-0001 Meetings: Oncologic Drugs Advisory Committee Notice NM-Notice of Meeting 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-06T16:46:45Z 2010-30502 0 0 0900006480bafeac
FDA-2000-N-0163-0023 FDA Bacterial Vaccines & Related Biological Products FDA-2000-N-0163 Reclassifications of Category IIIA Biological Products, Bacterial Vaccines and Related Biological Products, etc.: Delmont Laboratories, Inc.; Denial of Request for Hearing and Revocation of License Notice NFR-Notice of Final Rule 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-06T17:22:07Z 2010-30441 0 0 0900006480bafeaf
FDA-2009-E-0584-0005 FDA FDA-2009-E-0584 Determination of Regulatory Review Period for Purposes of Patent Extension: Besivance Notice N-Notice 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-08T16:21:28Z 2010-30510 0 0 0900006480baff29
FDA-2010-N-0595-0001 FDA FDA-2010-N-0595 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Exports; Notification and Recordkeeping Requirements Notice N-Notice 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z 2011-02-05T04:59:59Z 2010-12-06T16:36:03Z 2010-30433 0 0 0900006480bafe8a
FDA-2010-E-0036-0004 FDA FDA-2010-E-0036 Determination of Regulatory Review Period for Purposes of Patent Extension; STELARA Notice N-Notice 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-06T20:53:16Z 2010-30512 0 0 0900006480bafc54
FDA-2010-E-0032-0004 FDA FDA-2010-E-0032 Determination of Regulatory Review Period for Purposes of Patent Extension: Stelara Notice N-Notice 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-06T17:40:07Z 2010-30512 0 0 0900006480baff07
FDA-2010-N-0001-0153 FDA FDA-2010-N-0001 Meetings: Peripheral and Central Nervous System Drugs Advisory Committee Notice NM-Notice of Meeting 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2010-12-06T17:28:55Z 2010-30501 0 0 0900006480bafed0
FDA-2009-D-0137-0025 FDA FDA-2009-D-0137 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance for Industry; Use of Serological Tests to Reduce Risk of Transmission of Trypanosoma cruzi Infection, etc. Notice 30 Day Proposed Information Collection 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z 2011-01-06T04:59:59Z 2016-10-28T18:34:06Z 2010-30404 0 0 0900006480bafe83
FDA-2009-D-0137-0026 FDA FDA-2009-D-0137 Guidance for Industry: Use of Serological Tests to Reduce Riskof Transmission of Trypanosoma cruzi Infection, etc. Notice Notice of Availability 2010-12-06T05:00:00Z 2010 12 2010-12-06T05:00:00Z   2016-10-28T18:39:30Z 2010-30405 0 0 0900006480baff0b
FDA-2009-D-0533-0008 FDA FDA-2009-D-0533 Guidance for Industry: Recommendations for Blood Establishments; Availability: Training of Back-UpPersonnel, Assessment of Blood Donor Suitability, and Reporting Certain Changes to an Approved Application Notice NAD-Notice of Availability of Data 2010-12-03T05:00:00Z 2010 12 2010-12-03T05:00:00Z   2010-12-03T19:53:33Z 2010-30388 0 0 0900006480bad6f5
FDA-1999-F-0056-0003 FDA National Fisheries Institute and the Louisiana Department of Agriculture FDA-1999-F-0056 National Fisheries Institute; Filing of Food Additive Petition (FAP 9M4682) Notice NFL-Notice of Filing 2010-12-03T05:00:00Z 2010 12 2010-12-03T05:00:00Z   2010-12-03T17:37:36Z   0 0 09000064804a61c6
FDA-2010-D-0566-0001 FDA FDA-2010-D-0566 Draft Guidance for Industry on Residual Solvents in Animal Drug Products; Questions and Answers;Availability Notice NAD-Notice of Availability of Data 2010-12-03T05:00:00Z 2010 12 2010-12-03T05:00:00Z 2011-02-02T04:59:59Z 2010-12-03T17:35:27Z 2010-30387 0 0 0900006480bad670
FDA-2010-N-0597-0001 FDA FDA-2010-N-0597 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Index of Legally Marketed Unapproved New Animal Drugs for Minor Species Notice 60 Day Proposed Information Collection 2010-12-03T05:00:00Z 2010 12 2010-12-03T05:00:00Z 2011-02-02T04:59:59Z 2016-12-08T14:14:19Z 2010-30335 0 0 0900006480bad543
FDA-2010-N-0266-0005 FDA FDA-2010-N-0266 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Study of ClinicalEfficacy Information in Professional Labeling and Direct-to-Consumer Print Advertisements for Prescription Drugs Notice N-Notice 2010-12-03T05:00:00Z 2010 12 2010-12-03T05:00:00Z 2011-01-04T04:59:59Z 2010-12-03T17:25:33Z 2010-30385 0 0 0900006480bad6f4
FDA-2010-N-0001-0151 FDA FDA-2010-N-0001 Meetings: Gastrointestinal Drugs Advisory Committee Notice NM-Notice of Meeting 2010-12-02T05:00:00Z 2010 12 2010-12-02T05:00:00Z   2010-12-02T18:04:06Z 2010-30274 0 0 0900006480babfeb
FDA-2010-N-0603-0001 FDA FDA-2010-N-0603 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Animal Drug User Fees and Fee Waivers and Reductions Notice N-Notice 2010-12-02T05:00:00Z 2010 12 2010-12-02T05:00:00Z 2011-02-01T04:59:59Z 2010-12-02T17:58:10Z 2010-30264 0 0 0900006480bac029
FDA-2010-N-0182-0003 FDA FDA-2010-N-0182 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Procedures for Safe and Sanitary Processing and Importing of Fish and Fishery Products Notice NAL-Notice of Approval 2010-12-02T05:00:00Z 2010 12 2010-12-02T05:00:00Z   2010-12-02T17:53:36Z 2010-30277 0 0 0900006480babf74
FDA-2010-N-0001-0149 FDA FDA-2010-N-0001 Food Advisory Committee; Notice of Meeting Notice NM-Notice of Meeting 2010-12-01T05:00:00Z 2010 12     2011-08-16T19:06:57Z 2010-30187 0 0 0900006480baaef2
FDA-2010-N-0001-0150 FDA FDA-2010-N-0001 Workshops: Food Labeling Notice NM-Notice of Meeting 2010-12-01T05:00:00Z 2010 12 2010-12-01T05:00:00Z   2010-12-01T20:48:06Z 2010-30191 0 0 0900006480baaf41
FDA-2010-N-0576-0001 FDA FDA-2010-N-0576 Requests for Supplemental Applications: Supplemental Funding under Food and Drug Administration'sConvener of Active Medical Product Surveillance Discussions Notice NI-Notice of Intent 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z   2010-11-30T17:35:37Z 2010-30054 0 0 0900006480ba953e
FDA-2010-M-0519-0002 FDA FDA-2010-M-0519 Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Notice NAL-Notice of Approval 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z   2010-11-30T17:29:06Z   0 0 0900006480ba9673
FDA-1996-M-0183-0001 FDA Home Access Health Corp.; PMA of the Home Access HIV-1 Test FDA-1996-M-0183 Home Access Health Corp.; Premarket Approval of the Home Access HIV-1 Test System Notice NAL-Notice of Approval 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z   2010-11-30T18:48:05Z   0 0 0900006480500b9a
FDA-2010-N-0594-0001 FDA FDA-2010-N-0594 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Focus Groups as Usedby Food and Drug Administration (All Food and Drug Administration Regulated Products) Notice N-Notice 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z 2011-02-01T04:59:59Z 2010-11-30T16:28:27Z 2010-30037 0 0 0900006480ba9035
FDA-2010-N-0588-0001 FDA FDA-2010-N-0588 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Exceptions or Alternatives to Labeling Requirements for Products Held by Strategic National Stockpile Notice N-Notice 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z 2011-02-01T04:59:59Z 2020-10-06T19:47:38Z 2010-30036 0 0 0900006480ba953f
FDA-2010-N-0583-0001 FDA FDA-2010-N-0583 Agency Information Collection Activities: Proposed Collection; Comment Request; Radioactive Drug Research Committees Notice 60 Day Proposed Information Collection 2010-11-30T05:00:00Z 2010 11 2010-11-30T05:00:00Z 2011-02-01T04:59:59Z 2015-03-09T12:22:51Z 2010-30038 0 0 0900006480ba90d1
FDA-2010-D-0589-0001 FDA FDA-2010-D-0589 Draft Guidance for Industry on Hospital-Acquired Bacterial Pneumonia and Ventilator-Associated Bacterial Pneumonia: Developing Drugs for Treatment; Availability Notice NAD-Notice of Availability of Data 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z 2011-03-01T04:59:59Z 2011-03-10T20:37:20Z 2010-29799 0 0 0900006480ba7c22
FDA-2010-N-0600-0001 FDA FDA-2010-N-0600 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Animal Drug User Fee Cover Sheet Notice 60 Day Proposed Information Collection 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z 2011-01-29T04:59:59Z 2017-06-08T13:21:26Z 2010-29820 0 0 0900006480ba7c1d
FDA-2007-D-0150-0008 FDA FDA-2007-D-0150 Guidance for Industry on Antibacterial Drug Products: Use of Noninferiority Studies to Support Approval Notice Notice of Availability 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z   2020-05-06T02:18:14Z 2010-29796 0 0 0900006480ba7bbf
FDA-2010-D-0590-0001 FDA FDA-2010-D-0590 Guidance for Industry and Food and Drug Administration Staff; Availability, etc.: Blood Lancet Labeling Notice NAD-Notice of Availability of Data 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z   2010-11-30T15:02:35Z 2010-29795 0 0 0900006480ba7c33
FDA-2010-M-0361-0002 FDA FDA-2010-M-0361 Medical Devices; Availabilty of Safety and Effectiveness Summaries for Premarket Approval Applications Notice NAL-Notice of Approval 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z   2010-11-29T15:04:46Z 2010-29731 0 0 0900006480ba7e6f
FDA-2010-D-0565-0001 FDA FDA-2010-D-0565 Draft Guidance for Industry and Food and Drug Administration Staff; Availability, etc.: Establishing Performance Characteristics of In Vitro Diagnostic Devices for Detection of Clostridium difficile Notice NAD-Notice of Availability of Data 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z 2011-03-01T04:59:59Z 2010-11-29T20:19:53Z 2010-29794 0 0 0900006480ba8169
FDA-2010-D-0584-0001 FDA FDA-2010-D-0584 Guidance for Industry on Abbreviated New Drug Applications; Availability: Impurities in Drug Products Notice Notice of Availability 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z   2020-05-05T20:23:44Z 2010-29896 0 0 0900006480ba7cc3
FDA-2010-N-0547-0001 FDA FDA-2010-N-0547 Clinical Development Programs for Sedation Products; Request for Assistance Notice N-Notice 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z 2011-01-29T04:59:59Z 2024-11-07T22:28:43Z 2010-29927 1 0 0900006480ba8187
FDA-2010-N-0601-0001 FDA FDA-2010-N-0601 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Current Good Manufacturing Practice Regulations for Medicated Feeds Notice 60 Day Proposed Information Collection 2010-11-29T05:00:00Z 2010 11 2010-11-29T05:00:00Z 2011-01-29T04:59:59Z 2024-11-07T22:28:33Z 2010-29928 1 0 0900006480ba7ce7

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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);