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withdrawn,object_id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-2009-N-0665-0077,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor; Isoflurane,Rule,Final Rule,2009-12-28T05:00:00Z,2009,12,,,2013-07-09T18:25:09Z,E9-30590,0,0,0900006480a72080
FDA-2009-N-0665-0076,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage Form New Animal Drugs: Polysulfated Glycosaminoglycan,Rule,Final Rule,2009-12-21T05:00:00Z,2009,12,,,2013-07-09T15:52:49Z,E9-30222,0,0,0900006480a6eff2
FDA-2009-N-0665-0068,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage Form New Animal Drugs; Insulin - Final Rule,Rule,Final Rule,2009-12-14T05:00:00Z,2009,12,,,2014-01-08T13:27:08Z,E9-29583,0,0,0900006480a6a16d
FDA-2009-N-0665-0070,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor,Rule,Final Rule,2009-12-14T05:00:00Z,2009,12,,,2013-07-09T18:26:32Z,E9-29627,0,0,0900006480a6a16e
FDA-2009-N-0665-0065,FDA,FDA-2009-N-0665,Oral Dosage Form New Animal Drugs: Chlortetracycline Powder - Final Rule,Rule,Final Rule,2009-11-30T05:00:00Z,2009,11,,,2014-01-08T12:45:23Z,E9-28468,0,0,0900006480a60309
FDA-2009-N-0665-0064,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor,Rule,Final Rule,2009-11-25T05:00:00Z,2009,11,2009-11-25T05:00:00Z,,2013-07-09T18:28:15Z,E9-28217,0,0,0900006480a5e995
FDA-1977-N-0013-0041,FDA,FDA-1977-N-0013,"Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Final Monograph; Technical Amendment",Rule,Final Rule,2009-11-25T05:00:00Z,2009,11,2009-11-25T05:00:00Z,,2019-02-22T12:55:02Z,E9-28296,0,0,0900006480a5e8d7
FDA-2009-N-0665-0061,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds; Melengestrol; Monensin; Tylosin,Rule,Final Rule,2009-11-23T05:00:00Z,2009,11,,,2013-07-09T18:06:51Z,E9-28019,0,0,0900006480a5c836
FDA-2009-N-0665-0063,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds; Change of Sponsor,Rule,Final Rule,2009-11-23T05:00:00Z,2009,11,,,2013-07-09T18:45:41Z,E9-28009,0,0,0900006480a5cd02
FDA-2009-N-0665-0055,FDA,FDA-2009-N-0665,Certain Other Dosage Form New Animal Drugs; Progesterone Intravaginal Inserts,Rule,Final Rule,2009-11-17T05:00:00Z,2009,11,,,2013-07-09T14:49:52Z,E9-27497,0,0,0900006480a592c7
FDA-2007-C-0456-0002,FDA,FDA-2007-C-0456,Listing of Color Additives Exempt From Certification; Paracoccus Pigment,Rule,NFR-Notice of Final Rule,2009-11-16T05:00:00Z,2009,11,2009-11-16T05:00:00Z,2009-12-17T04:59:59Z,2026-01-02T23:03:56Z,E9-27394,0,0,0900006480a582d1
FDA-2009-N-0666-0003,FDA,FDA-2009-N-0666,New Animal Drugs in Genetically Engineered Animals,Rule,CFR-Correction,2009-11-12T05:00:00Z,2009,11,2009-11-12T05:00:00Z,,2009-11-12T14:55:34Z,E9-27305,0,0,0900006480a5600f
FDA-2009-N-0464-0001,FDA,FDA-2009-N-0464,Investigational New Drug Applications; Technical Amendment,Rule,NFR-Notice of Final Rule,2009-10-29T04:00:00Z,2009,10,,,2009-10-29T18:43:42Z,E9-26095,0,0,0900006480a4d85f
FDA-2009-N-0472-0001,FDA,FDA-2009-N-0472,Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Cardiac Allograft,Rule,NFR-Notice of Final Rule,2009-10-21T04:00:00Z,2009,10,2009-10-21T04:00:00Z,,2009-10-21T20:51:55Z,E9-25315,0,0,0900006480a47214
FDA-1977-N-0225-0001,FDA,FDA-1977-N-0225,Polychlorinated Biphenyls (PCB's),Rule,Final Rule,2009-09-25T04:00:00Z,2009,9,,,2020-04-28T12:20:16Z,77-7519,0,0,09000064805ecf64
FDA-2009-N-0665-0047,FDA,FDA-2009-N-0665,Ophthalmic and Topical Dosage Form New Animal Drugs; Diclofenac,Rule,Final Rule,2009-09-16T04:00:00Z,2009,9,2009-09-16T04:00:00Z,,2013-07-09T16:18:44Z,E9-22292,0,0,0900006480a2469d
FDA-1979-N-0319-0003,FDA,FDA-1979-N-0319,Part 172-- Food Additives Permitted for Direct Addition to Food for Human Consumption; Sodium Stearoyl-2-Lactylate,Rule,Final Rule,2009-08-31T04:00:00Z,2009,8,2009-08-31T04:00:00Z,1980-09-06T03:59:59Z,2019-06-27T12:23:27Z,80-23303,0,0,0900006480555c16
FDA-1993-P-0085-0004,FDA,FDA-1993-P-0085,Diacetyl Tartaric Acid Esters of Mono-and Diglycerides; Revision of Common or Usual Name,Rule,NFR-Notice of Final Rule,2009-08-28T04:00:00Z,2009,8,2009-08-28T04:00:00Z,,2009-08-29T01:58:50Z,,0,0,09000064804fd4e5
FDA-2009-N-0381-0001,FDA,FDA-2009-N-0381,Advisory Committee; Tobacco Products Scientific Advisory Committee; Establishment,Rule,NFR-Notice of Final Rule,2009-08-26T04:00:00Z,2009,8,2009-08-26T04:00:00Z,,2009-08-26T16:21:49Z,E9-20485,0,0,0900006480a12f27
FDA-2008-N-0176-0009,FDA,FDA-2008-N-0176,"Defining ""Small Number of Animals"" for Minor Use Designation",Rule,NFR-Notice of Final Rule,2009-08-26T04:00:00Z,2009,8,2009-08-26T04:00:00Z,,2011-06-11T16:27:43Z,E9-20553,0,0,0900006480a12f05
FDA-2009-N-0344-0002,FDA,FDA-2009-N-0344,Microbiology Devices; Reclassification of Herpes Simplex Virus Types 1 and 2 Serological Assays,Rule,NFR-Notice of Final Rule,2009-08-25T04:00:00Z,2009,8,2009-08-25T04:00:00Z,2009-11-10T04:59:59Z,2009-08-25T17:11:12Z,E9-20411,0,0,0900006480a11be7
FDA-2009-N-0100-0003,FDA,FDA-2009-N-0100,Revision of the Requirements for Publication of License Revocation; Confirmation of Effective Date,Rule,NCD-Notice of Confirmation of Effective Date,2009-08-21T04:00:00Z,2009,8,,,2009-08-21T16:34:42Z,E9-20119,0,0,0900006480a0f501
FDA-2009-N-0665-0045,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds: Semduramicin; Virginiamycin,Rule,Final Rule,2009-08-18T04:00:00Z,2009,8,,,2013-07-09T16:26:50Z,E9-19738,0,0,0900006480a0c245
FDA-2006-N-0238-0026,FDA,FDA-2006-N-0238,Expanded Access to Investigational Drugs for Treatment Use,Rule,NFR-Notice of Final Rule,2009-08-13T04:00:00Z,2009,8,2009-08-13T04:00:00Z,,2015-06-02T18:01:51Z,E9-19005,0,0,0900006480a084e7
FDA-2009-N-0665-0044,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds: Oxytetracycline; Neomycin,Rule,Final Rule,2009-08-13T04:00:00Z,2009,8,2009-08-13T04:00:00Z,,2013-07-09T18:03:19Z,E9-19414,0,0,0900006480a08523
FDA-2006-N-0237-0049,FDA,FDA-2006-N-0237,Notice of Final Rule re Charging for Investigational Drugs Under an Investigational New Drug Application,Rule,Final Rule,2009-08-13T04:00:00Z,2009,8,2009-08-13T04:00:00Z,,2016-02-09T20:59:52Z,E9-19004,0,0,0900006480a08453
FDA-2009-N-0666-0002,FDA,FDA-2009-N-0666,Use of Ozone-Depleting Substances; Epinephrine; CFR Correction,Rule,NCR-Notice of Correction,2009-08-11T04:00:00Z,2009,8,,,2009-08-11T17:57:32Z,E9-19297,0,0,0900006480a05856
FDA-2008-N-0163-0250,FDA,FDA-2008-N-0163,"Dental Devices: Classification of Dental Amalgam, Reclassification of Dental Mercury, Designation of Special Controls for Dental Amalgam, Mercury, and Amalgam Alloy; Final Rule",Rule,NFR-Notice of Final Rule,2009-08-04T04:00:00Z,2009,8,2009-08-04T04:00:00Z,,2011-06-11T16:27:42Z,E9-18447,0,0,0900006480a00973
FDA-2008-N-0163-0249,FDA,FDA-2008-N-0163,"Dental Devices: Classification of Dental Amalgam, Reclassification of Dental Mercury, Designation of Special Controls for Dental Amalgam, Mercury, and Amalgam Alloy",Rule,,2009-08-04T00:00:00Z,2009,8,,,2011-06-11T16:27:42Z,,0,1,0900006480a007e1
FDA-2009-N-0665-0042,FDA,FDA-2009-N-0665,New Animal Drugs: Nitrofurazone Ointment - Final Rule,Rule,Final Rule,2009-08-03T04:00:00Z,2009,8,2009-08-03T04:00:00Z,,2014-01-08T12:47:59Z,E9-18337,0,0,09000064809ffeea
FDA-2008-N-0341-0006,FDA,FDA-2008-N-0341,Applications for Food and Drug Administration Approval To Market a New Drug; Postmarketing Reports; Reporting Information About Authorized Generic Drugs,Rule,NFR-Notice of Final Rule,2009-07-28T04:00:00Z,2009,7,2009-07-28T04:00:00Z,,2011-06-11T16:27:46Z,E9-17963,0,0,09000064809fc2ed
FDA-2009-N-0316-0001,FDA,FDA-2009-N-0316,New Drug Applications and Abbreviated New Drug Applications; Technical Amendment,Rule,NFR-Notice of Final Rule,2009-07-24T04:00:00Z,2009,7,2009-07-24T04:00:00Z,,2009-07-24T14:27:40Z,E9-17680,0,0,09000064809fa1ef
FDA-2009-N-0270-0001,FDA,FDA-2009-N-0270,"Animal Drugs, Feeds, and Related Products; Withdrawal of Approval of New Animal Drug Applications",Rule,NFR-Notice of Final Rule,2009-07-22T04:00:00Z,2009,7,2009-07-22T04:00:00Z,,2009-07-22T16:14:22Z,E9-17409,0,0,09000064809f7d5a
FDA-2009-N-0665-0041,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor,Rule,Final Rule,2009-07-22T04:00:00Z,2009,7,2009-07-22T04:00:00Z,,2013-07-09T18:39:29Z,E9-17356,0,0,09000064809f783c
FDA-2009-N-0310-0001,FDA,FDA-2009-N-0310,Advisory Committee; Risk Communication Advisory Committee; Termination and Recharter,Rule,NFR-Notice of Final Rule,2009-07-21T04:00:00Z,2009,7,2009-07-21T04:00:00Z,,2009-07-21T16:40:59Z,E9-17218,0,0,09000064809f722e
FDA-1995-F-0403-0002,FDA,FDA-1995-F-0403,Secondary Direct Food Additives Permitted in Food for Human Consumption,Rule,NFR-Notice of Final Rule,2009-07-20T04:00:00Z,2009,7,2009-07-20T04:00:00Z,1996-10-04T03:59:59Z,2009-07-22T02:57:56Z,,0,0,090000648059aeba
FDA-2009-N-0665-0035,FDA,FDA-2009-N-0665,New Animal Drugs; Ceftiofur Sodium - Final Rule,Rule,Final Rule,2009-07-15T04:00:00Z,2009,7,2009-07-15T04:00:00Z,,2014-01-08T12:49:23Z,E9-16734,0,0,09000064809f1cf3
FDA-2009-N-0665-0039,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds; Lasalocid; Roxarsone,Rule,Final Rule,2009-07-15T04:00:00Z,2009,7,2009-07-15T04:00:00Z,,2013-07-09T14:20:50Z,E9-16733,0,0,09000064809f1daf
FDA-2009-N-0665-0037,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage Form New Animal Drugs; Flunixin - Final Rule,Rule,Final Rule,2009-07-15T04:00:00Z,2009,7,2009-07-15T04:00:00Z,,2014-01-07T21:46:03Z,E9-16735,0,0,09000064809f1d64
FDA-2000-N-0190-0018,FDA,FDA-2000-N-0190,"Prevention of Salmonella Enteritidis in Shell Eggs During Production, Storage, and Transportation",Rule,NFR-Notice of Final Rule,2009-07-09T04:00:00Z,2009,7,2009-07-09T04:00:00Z,,2011-06-11T16:25:52Z,E9-16119,0,0,09000064809ed1eb
FDA-1977-N-0013-0037,FDA,FDA-1977-N-0013,"Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Final Monograph; Corrections",Rule,Correction,2009-06-30T04:00:00Z,2009,6,2009-06-30T04:00:00Z,,2019-02-21T21:46:48Z,E9-15403,0,0,09000064809e636f
FDA-1991-E-0155-0002,FDA,FDA-1991-E-0155,"U.S. Patent and Trademark Office to Louis Gubinsky (Sughrue, Mion, Zinn, MacPeak & Seas) - Certificate Extending Patent Term",Rule,Certificate Extending Patent Term,2009-06-26T04:00:00Z,2009,6,2009-06-26T04:00:00Z,,2023-07-24T19:25:47Z,,0,0,090000648052d1ed
FDA-1989-F-0343-0002,FDA,FDA-1989-F-0343,Food Additives Permitted for Direct Addition to Food for Human Consumption; Sucrose Fatty Acid Esters,Rule,Final Rule,2009-06-19T04:00:00Z,2009,6,2009-06-19T04:00:00Z,1995-09-29T03:59:59Z,2023-12-29T13:54:30Z,,0,0,0900006480479f36
FDA-1989-F-0333-0002,FDA,FDA-1989-F-0333,Food Additives Permitted for Direct Addition to Food fo Human Consumption; Sucrose Fatty Acid Esters,Rule,NFR-Notice of Final Rule,2009-06-19T04:00:00Z,2009,6,2009-06-19T04:00:00Z,1995-09-29T03:59:59Z,2009-06-19T23:40:56Z,,0,0,0900006480479ebe
FDA-1992-F-0213-0002,FDA,FDA-1992-F-0213,Food Additives Permitted for Direct Addition to Food for Human Consumption; Sucrose Fatty Acid Esters,Rule,NFR-Notice of Final Rule,2009-06-19T04:00:00Z,2009,6,2009-06-19T04:00:00Z,1995-09-29T03:59:59Z,2009-06-19T23:20:54Z,,0,0,090000648052fa1d
FDA-2009-N-0665-0030,FDA,FDA-2009-N-0665,Oral Dosage Form New Animal Drugs; Toceranib - Final Rule,Rule,Final Rule,2009-06-18T04:00:00Z,2009,6,2009-06-18T04:00:00Z,,2014-01-08T13:24:48Z,E9-14299,0,0,09000064809d24c0
FDA-2009-N-0665-0029,FDA,FDA-2009-N-0665,New Animal Drugs for Use in Animal Feeds; Chlortetracycline,Rule,Final Rule,2009-06-12T04:00:00Z,2009,6,2009-06-12T04:00:00Z,,2013-07-09T18:20:51Z,E9-13849,0,0,09000064809cdaa9
FDA-2009-N-0665-0027,FDA,FDA-2009-N-0665,Oral Dosage Form New Animal Drugs: Methimazole - Final Rule,Rule,Final Rule,2009-06-11T04:00:00Z,2009,6,2009-06-11T04:00:00Z,,2014-01-08T13:12:43Z,E9-13685,0,0,09000064809cc342
FDA-2009-N-0665-0026,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor; Fomepizole,Rule,Final Rule,2009-06-05T04:00:00Z,2009,6,2009-06-05T04:00:00Z,,2013-07-09T15:59:42Z,E9-13126,0,0,09000064809c67a5
FDA-2009-N-0665-0025,FDA,FDA-2009-N-0665,Ophthalmic and Topical Dosage Form New Animal Drugs; Change of Sponsor; Diclofenac; Ivermectin Otic Suspension - Final Rule,Rule,Final Rule,2009-06-04T04:00:00Z,2009,6,2009-06-04T04:00:00Z,,2014-01-08T13:44:43Z,E9-13015,0,0,09000064809c4ae9
FDA-2008-N-0446-0016,FDA,FDA-2008-N-0446,Beverages: Bottled Water,Rule,NFR-Notice of Final Rule,2009-05-29T04:00:00Z,2009,5,2009-05-29T04:00:00Z,,2009-05-29T15:29:41Z,E9-12494,0,0,09000064809be76c
FDA-2009-N-0665-0024,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage Form New Animal Drugs; Change of Sponsor; Luprostiol,Rule,Final Rule,2009-05-27T04:00:00Z,2009,5,2009-05-27T04:00:00Z,,2013-07-09T17:58:46Z,E9-12269,0,0,09000064809b8f02
FDA-1991-E-0282-0004,FDA,FDA-1991-E-0282,U.S. Patent and Trademark Office - Certificate Extending Patent,Rule,CEP-Certificate Extending Patent Term,2009-05-14T04:00:00Z,2009,5,2009-05-14T04:00:00Z,,2009-05-14T21:35:17Z,,0,0,090000648052fa55
FDA-2009-N-0665-0019,FDA,FDA-2009-N-0665,New Animal Drugs: Trilostane - Final Rule,Rule,Final Rule,2009-05-11T04:00:00Z,2009,5,2009-05-11T04:00:00Z,,2014-01-08T13:14:27Z,E9-10927,0,0,0900006480987dc5
FDA-2009-N-0665-0018,FDA,FDA-2009-N-0665,New Animal Drugs: Carprofen - Final Rule,Rule,Final Rule,2009-05-11T04:00:00Z,2009,5,2009-05-11T04:00:00Z,,2014-01-07T21:42:40Z,E9-10925,0,0,0900006480987da1
FDA-2009-N-0665-0016,FDA,FDA-2009-N-0665,New Animal Drugs; Change of Sponsor,Rule,NFR-Notice of Final Rule,2009-05-05T04:00:00Z,2009,5,2009-05-05T04:00:00Z,,2009-05-05T16:02:55Z,E9-10262,0,0,0900006480975f81
FDA-2009-N-0665-0017,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage From New Animal Drugs; Change of Sponsor; Repository Corticotropin Injection,Rule,Final Rule,2009-05-05T04:00:00Z,2009,5,2009-05-05T04:00:00Z,,2013-07-09T18:36:17Z,E9-10291,0,0,0900006480975fc4
FDA-2002-N-0031-0398,FDA,FDA-2002-N-0031,Substances Prohibited From Use in Animal Food or Feed; Confirmation of Effective Date of Final Rule; Correction,Rule,NCR-Notice of Correction,2009-05-05T04:00:00Z,2009,5,2009-05-05T04:00:00Z,,2011-06-11T16:25:52Z,E9-10138,0,0,0900006480975fcc
FDA-2009-N-0100-0001,FDA,FDA-2009-N-0100,Revision of the Requirements for Publication of License Revocation,Rule,NFR-Notice of Final Rule,2009-05-05T04:00:00Z,2009,5,2009-05-05T04:00:00Z,2009-07-21T03:59:59Z,2009-05-05T15:50:19Z,E9-10244,0,0,0900006480975f36
FDA-2009-N-0665-0015,FDA,FDA-2009-N-0665,Ophthalmic and Topical Dosage Form New Animal Drugs; Selamectin,Rule,Final Rule,2009-04-30T04:00:00Z,2009,4,2009-04-30T04:00:00Z,,2013-07-09T16:13:59Z,E9-09901,0,0,090000648096fd38
FDA-1977-N-0013-0017,FDA,FDA-1977-N-0013,"Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Final Monograph",Rule,Final Rule,2009-04-29T04:00:00Z,2009,4,2009-04-29T04:00:00Z,,2019-03-20T19:57:29Z,E9-9684,0,0,090000648096ef53
FDA-2009-N-0665-0014,FDA,FDA-2009-N-0665,"Intramammary Dosage Forms:  Change of Sponsor,",Rule,Final Rule,2009-04-27T04:00:00Z,2009,4,2009-04-27T04:00:00Z,,2013-07-09T18:31:07Z,E9-09527,0,0,090000648096d22e
FDA-2002-N-0031-0397,FDA,FDA-2002-N-0031,Substances Prohibited From Use in Animal Food or Feed; Confirmation of Effective Date of Final Rule,Rule,NCD-Notice of Confirmation of Effective Date,2009-04-24T04:00:00Z,2009,4,,,2011-06-11T16:25:53Z,E9-09466,0,0,0900006480968c71
FDA-2009-N-0144-0001,FDA,FDA-2009-N-0144,Revision of Organization and Conforming Changes to Regulations,Rule,NIR-Notice of Interim Rule,2009-04-01T04:00:00Z,2009,4,2009-04-01T04:00:00Z,,2009-04-01T18:38:04Z,E9-07349,0,0,090000648093b13b
FDA-2009-N-0141-0001,FDA,FDA-2009-N-0141,Medical Devices; Technical Amendment,Rule,NFR-Notice of Final Rule,2009-03-31T04:00:00Z,2009,3,2009-03-31T04:00:00Z,,2009-03-31T16:58:22Z,E9-07073,0,0,0900006480939356
FDA-2009-N-0666-0001,FDA,FDA-2009-N-0666,New Animal Drugs for Use in Animal Feeds; CFR Correction,Rule,CFR-Correction,2009-03-26T04:00:00Z,2009,3,,,2009-03-26T18:02:55Z,E9-06810,0,0,09000064809306b9
FDA-2005-F-0505-0002,FDA,FDA-2005-F-0505,Food Additives Permitted for Direct Addition to Food for Human Consumption; Silver Nitrate and Hydrogen Peroxide,Rule,Final Rule,2009-03-18T04:00:00Z,2009,3,2009-03-18T04:00:00Z,2009-04-18T03:59:59Z,2025-11-26T20:21:30Z,E9-05852,0,0,090000648091b633
FDA-2007-F-0274-0002,FDA,FDA-2007-F-0274,Food Additives Permitted for Direct Addition to Food for Human Consumption: Vitamin D,Rule,NFR-Notice of Final Rule,2009-03-16T04:00:00Z,2009,3,2009-03-16T04:00:00Z,2009-04-16T03:59:59Z,2026-01-03T00:14:06Z,E9-05549,0,0,09000064809146e6
FDA-1998-P-0032-0006,FDA,FDA-1998-P-0032,"Listing of Color Additives Exempt From Certification; Food, Drug, and Cosmetic Labeling: Cochineal Extract and Carmine Declaration; Confirmation of Effective Date",Rule,Confirmation of Effective Date,2009-03-11T04:00:00Z,2009,3,2009-03-11T04:00:00Z,,2016-03-21T17:25:55Z,E9-05286,0,0,090000648090520b
FDA-2009-N-0665-0009,FDA,FDA-2009-N-0665,Other Dosage Form New Animal Drugs: Sevoflurane,Rule,Final Rule,2009-03-11T04:00:00Z,2009,3,2009-03-11T04:00:00Z,,2013-07-09T16:13:07Z,E9-04879,0,0,090000648090506a
FDA-2009-N-0665-0010,FDA,FDA-2009-N-0665,Oral Dosage Form New Animal Drugs: Amprolium - Final Rule,Rule,Final Rule,2009-03-11T04:00:00Z,2009,3,2009-03-11T04:00:00Z,,2014-01-07T21:51:09Z,E9-05131,0,0,09000064809050a7
FDA-2009-N-0665-0006,FDA,FDA-2009-N-0665,Implantation or Injectable Dosage Form New Animal Drugs; Ivermectin - Final Rule,Rule,Final Rule,2009-03-02T05:00:00Z,2009,3,2009-03-02T05:00:00Z,,2014-01-08T13:47:58Z,E9-04304,0,0,09000064808e61ca
FDA-2008-N-0561-0004,FDA,FDA-2008-N-0561,"Maximum Civil Money Penalty Amounts and Compliance, etc.: Confirmation of Effective Date",Rule,NFR-Notice of Final Rule,2009-02-24T05:00:00Z,2009,2,2009-02-24T05:00:00Z,,2009-02-24T17:31:27Z,E9-03831,0,0,09000064808d6e38
FDA-2009-N-0665-0001,FDA,FDA-2009-N-0665,New Animal Drugs: Bc6 Recombinant Deoxyribonucleic Acid Construct,Rule,NFR-Notice of Final Rule,2009-02-11T05:00:00Z,2009,2,2009-02-11T05:00:00Z,,2009-02-11T20:28:59Z,E9-02881,0,0,0900006480852428
FDA-2008-N-0341-0005,FDA,FDA-2008-N-0341,Applications for Food and Drug Administration Approval to Market a New Drug; Postmarketing Reports: Reporting Information about Authorized Generic Drugs; Withdrawal,Rule,NWL-Notice of Withdrawl,2009-02-10T05:00:00Z,2009,2,2009-02-10T05:00:00Z,,2009-02-10T20:16:46Z,E9-02746,0,0,090000648084f5c8
FDA-2008-N-0039-0095,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs: Ivermectin Paste - Final Rule,Rule,Final Rule,2009-02-10T05:00:00Z,2009,2,2009-02-10T05:00:00Z,,2014-01-08T14:11:50Z,E9-02749,0,0,090000648084f677
FDA-1982-N-0010-0007,FDA,FDA-1982-N-0010,Vitamin D2 & D3 Proposed Affirmation of GRAS Status; with Specific Limitations as Direct Human Food Ingredients,Rule,NFR-Notice of Final Rule,2009-01-21T05:00:00Z,2009,1,2009-01-21T05:00:00Z,,2009-01-22T00:41:41Z,,0,0,0900006480829bdf
FDA-2008-N-0039-0094,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs: Phenylbutazone Tablets and Boluses,Rule,Final Rule,2009-01-12T05:00:00Z,2009,1,2009-01-12T05:00:00Z,,2013-07-09T19:32:23Z,E9-00265,0,0,090000648081b72e
FDA-1998-P-0032-0002,FDA,FDA-1998-P-0032,"Listing of Color Additives Exempt From Certification; Food, Drug, and Cosmetic Labeling: Cochineal Extract and Carmine Declaration",Rule,Final Rule,2009-01-05T05:00:00Z,2009,1,2009-01-05T05:00:00Z,2009-02-05T04:59:59Z,2024-11-12T04:34:59Z,,1,0,090000648080f0f8
FDA-2008-N-0517-0001,FDA,FDA-2008-N-0517,"Medical, Immunology and Microbiology Devices: Classification of Enterovirus Nucleic Acid Assay",Rule,NFR-Notice of Final Rule,2009-01-02T05:00:00Z,2009,1,2009-01-02T05:00:00Z,,2009-01-09T03:28:05Z,E8-31213,0,0,090000648080c365
FDA-2008-N-0039-0093,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feeds; Tiamulin,Rule,Final Rule,2009-01-02T05:00:00Z,2009,1,2009-01-02T05:00:00Z,,2013-07-09T19:38:10Z,E8-31128,0,0,090000648080c33b