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withdrawn,object_id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-2008-N-0039-0098,FDA,FDA-2008-N-0039,"Supplement Abbreviated New Animal Drug Application; Flunazine, (flunixin meglumine), Injectable Solution, Horses and Cattle - Freedom of Information Summary",Supporting & Related Material,Freedom of Information Summary,2009-02-12T05:00:00Z,2009,2,,,2014-01-08T14:19:17Z,,0,0,09000064808548d1
FDA-2008-N-0039-0097,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs: Flunixin - Final Rule,Notice,Notice of Final Rule,2009-02-12T05:00:00Z,2009,2,,,2014-01-08T14:17:02Z,E9-02941,0,0,09000064808545a3
FDA-2008-N-0039-0096,FDA,FDA-2008-N-0039,"Supplemental Abbreviated New Animal Drug Application - PHOENECTIN Paste 1.87%, (ivermectin), Oral Paste-Horses - Freedom of Information Summary",Supporting & Related Material,Freedom of Information Summary,2009-02-10T05:00:00Z,2009,2,,,2014-01-08T14:16:01Z,,0,0,090000648084fa4c
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-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-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
FDA-2008-N-0039-0092,FDA,FDA-2008-N-0039,Freedom of Information Summary - Original Abbreviated New Drug Application - ANADA 200-459,Supporting & Related Material,Freedom of Information Summary,2008-12-29T05:00:00Z,2008,12,,,2013-07-09T18:51:04Z,,0,0,0900006480805f78
FDA-2008-N-0039-0091,FDA,FDA-2008-N-0039,Ophthalmic and Topical Dosage Form New Animal Drugs; Triamcinolone Cream,Rule,Final Rule,2008-12-29T05:00:00Z,2008,12,2008-12-29T05:00:00Z,,2013-07-09T18:48:19Z,E8-30694,0,0,0900006480805eeb
FDA-2008-N-0039-0090,FDA,FDA-2008-N-0039,Freedom of Information Summary - NADA 013-076 - TYLAN Soluble Tylosin tartrate Soluble powder Swine,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-12-18T05:00:00Z,2008,12,,,2008-12-20T16:29:53Z,,0,0,09000064807e0877
FDA-2008-N-0039-0089,FDA,FDA-2008-N-0039,Freedom of Information Summary - NADA 012-491 - TYLAN 40 and TYLAN 100 Tylosin phosphate,Supporting & Related Material,Freedom of Information Summary,2008-12-18T05:00:00Z,2008,12,,,2013-07-11T14:46:49Z,,0,0,09000064807e084d
FDA-2008-N-0039-0088,FDA,FDA-2008-N-0039,New Animal Drugs; Tylosin,Notice,Notice of Final Rule,2008-12-18T05:00:00Z,2008,12,,,2013-07-11T14:42:33Z,E8-29861,0,0,09000064807e0691
FDA-2008-N-0039-0086,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feeds; Ractopamine,Notice,Notice of Final Rule,2008-12-11T05:00:00Z,2008,12,,,2013-07-09T20:00:14Z,E8-29177,0,0,09000064807d7057
FDA-2008-N-0039-0087,FDA,FDA-2008-N-0039,"Freedom of Information (FOI) Summary - Optaflexx (ractopamine hydrochloride), Rumensin (monensin sodium) Tylan (tylosin phosphate) and HEIFERMAX 500 (melengestrol acetate)",Supporting & Related Material,Freedom of Information Summary,2008-12-11T05:00:00Z,2008,12,,,2013-07-09T20:02:52Z,,0,0,09000064807d7224
FDA-2008-N-0039-0083,FDA,FDA-2008-N-0039,Freedom of Information Summary - Original New Animal Drug Application - NADA 141-290 - TOPMAX 9 (Ractopamine Hydrochloride) Type A Medicated Article Finishing Turkeys,Supporting & Related Material,Freedom of Information Summary,2008-12-01T05:00:00Z,2008,12,,,2013-07-10T16:18:47Z,,0,0,09000064807c743a
FDA-2008-N-0039-0084,FDA,FDA-2008-N-0039,Environmental Assessment For the Use of Topmax® in the Feed of Turkeys,Supporting & Related Material,Environmental Assessment,2008-12-01T05:00:00Z,2008,12,,,2013-07-10T16:22:43Z,,0,0,09000064807c7469
FDA-2008-N-0039-0082,FDA,FDA-2008-N-0039,New Animal Drugs; Ractopamine,Rule,Final Rule,2008-12-01T05:00:00Z,2008,12,2008-12-01T05:00:00Z,,2013-07-10T16:15:59Z,E8-28384,0,0,09000064807c7111
FDA-2008-N-0039-0085,FDA,FDA-2008-N-0039,Finding of No Significant Impact - Topmax® (Ractopamine HCl) in the Feed of Turkeys,Supporting & Related Material,Finding of no Significant Impact,2008-12-01T05:00:00Z,2008,12,,,2013-07-10T16:25:00Z,,0,0,09000064807c7491
FDA-2008-N-0039-0081,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Amprolium; Correction,Rule,Correction,2008-11-20T05:00:00Z,2008,11,2008-11-20T05:00:00Z,,2013-07-11T14:19:15Z,E8-27646,0,0,09000064807b36b5
FDA-2008-N-0039-0079,FDA,FDA-2008-N-0039,Approval of Original Abbreviated New Animal Drug Application; Phenylbutazone Tablets,Notice,Notice of Approval,2008-11-12T05:00:00Z,2008,11,,,2013-07-09T19:53:18Z,E8-26793,0,0,09000064807a4da6
FDA-2008-N-0039-0080,FDA,FDA-2008-N-0039,Freedom of Information (FOI) Summary - FOIS,Supporting & Related Material,Freedom of Information Summary,2008-11-12T05:00:00Z,2008,11,,,2013-07-09T19:57:19Z,,0,0,09000064807a4f83
FDA-2008-N-0039-0078,FDA,FDA-2008-N-0039,Freedom of Information Summary - FOIS,Supporting & Related Material,Freedom of Information Summary,2008-10-31T04:00:00Z,2008,10,,,2013-07-10T18:59:33Z,,0,0,090000648078785b
FDA-2008-N-0039-0077,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Firocoxib Tablets,Rule,Final Rule,2008-10-31T04:00:00Z,2008,10,,,2013-07-10T18:54:17Z,E8-26020,0,0,090000648078769c
FDA-2008-N-0039-0071,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin,Rule,Final Rule,2008-10-08T04:00:00Z,2008,10,2008-10-08T04:00:00Z,,2013-07-10T18:24:50Z,E8-23832,0,0,090000648073e0bc
FDA-2008-N-0039-0075,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Ceftiofur Crystalline Free Acid,Rule,Final Rule,2008-10-08T04:00:00Z,2008,10,2008-10-08T04:00:00Z,,2013-07-10T19:01:42Z,E8-23830,0,0,090000648073e103
FDA-2008-N-0039-0074,FDA,FDA-2008-N-0039,Safe-Guard (Fenbendazole) - Freedom of Information Summary,Supporting & Related Material,Freedom of Information Summary,2008-10-08T04:00:00Z,2008,10,,,2013-07-10T20:13:33Z,,0,0,090000648073e4e2
FDA-2008-N-0039-0076,FDA,FDA-2008-N-0039,Excede (Ceftiofur Crystalline Free Acid) Sterile Suspension - Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-10-08T04:00:00Z,2008,10,,,2013-07-10T19:04:11Z,,0,0,090000648073e577
FDA-2008-N-0039-0072,FDA,FDA-2008-N-0039,Draxxin (Tulathromycin) Injectable Solution - Freedom of Information Summary,Supporting & Related Material,Freedom of Information Summary,2008-10-08T04:00:00Z,2008,10,,,2013-07-10T18:28:38Z,,0,0,090000648073e476
FDA-2008-N-0039-0073,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feeds; Fenbendazole,Rule,Final Rule,2008-10-08T04:00:00Z,2008,10,2008-10-08T04:00:00Z,,2013-07-10T20:10:36Z,E8-23845,0,0,090000648073e0ff
FDA-2008-N-0039-0070,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Sulfadiazine/Pyrimethamine Suspension,Rule,Final Rule,2008-09-17T04:00:00Z,2008,9,2008-09-17T04:00:00Z,,2013-07-10T18:41:20Z,E8-21625,0,0,090000648070a75b
FDA-2008-N-0039-0068,FDA,FDA-2008-N-0039,Chloramine-T for Control of Bacterial Gill Disease in Freshwater- Reared Salmonids; Availability of Data,Notice,Notice of Availability,2008-08-21T04:00:00Z,2008,8,,,2013-07-11T14:27:19Z,E8-19299,0,0,09000064806d1357
FDA-2008-N-0039-0069,FDA,FDA-2008-N-0039,Freedom of Information Summary Chloramine - T Soluble Powder for Immersion Freshwater - reared salmonids - FOIS,Supporting & Related Material,Freedom of Information Summary,2008-08-21T04:00:00Z,2008,8,,,2013-07-11T14:29:57Z,,0,0,09000064806d152a
FDA-2008-N-0039-0065,FDA,FDA-2008-N-0039,Freedom of Information Summary [New Animal Drugs For Use in Animal Feeds; Oxytetracycline - NADA 38-439] - FOIS,Supporting & Related Material,Freedom of Information Summary,2008-08-07T04:00:00Z,2008,8,,,2013-07-11T13:49:07Z,,0,0,09000064806b4494
FDA-2008-N-0039-0064,FDA,FDA-2008-N-0039,New Animal Drugs For Use in Animal Feeds; Oxytetracycline,Rule,Final Rule,2008-08-07T04:00:00Z,2008,8,,,2013-07-11T13:44:20Z,E8-18129,0,0,09000064806b4074
FDA-2008-N-0039-0067,FDA,FDA-2008-N-0039,See FDA-2008-N-0039-0066.1,Supporting & Related Material,Environmental Assessment,2008-08-07T04:00:00Z,2008,8,,,2013-07-11T13:56:58Z,,0,0,09000064806b46f9
FDA-2008-N-0039-0066,FDA,FDA-2008-N-0039,Finding of No Significant Impact [New Animal Drugs For Use in Animal Feeds; Oxytetracycline - NADA 38-439]- FONSI,Supporting & Related Material,Freedom of Information Summary,2008-08-07T04:00:00Z,2008,8,,,2013-07-11T13:53:14Z,,0,0,09000064806b44c9
FDA-2008-N-0039-0060,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Amprolium,Rule,Final Rule,2008-08-06T04:00:00Z,2008,8,2008-08-06T04:00:00Z,,2013-07-11T14:22:57Z,E8-18093,0,0,09000064806b15a2
FDA-2008-N-0039-0063,FDA,FDA-2008-N-0039,Ceftiofur Hydrochloride (Excenel Rtu Ez) Sterile Suspension - Freedom of Information Summary,Supporting & Related Material,Freedom of Information Summary,2008-08-06T04:00:00Z,2008,8,,,2013-07-10T16:31:44Z,,0,0,09000064806b1a9b
FDA-2008-N-0039-0061,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Oxfendazole Suspension,Rule,Final Rule,2008-08-06T04:00:00Z,2008,8,2008-08-06T04:00:00Z,,2013-07-10T19:50:02Z,E8-18092,0,0,09000064806b161e
FDA-2008-N-0039-0062,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Ceftiofur Hydrochloride,Rule,Final Rule,2008-08-06T04:00:00Z,2008,8,2008-08-06T04:00:00Z,,2013-07-10T16:28:17Z,E8-18094,0,0,09000064806b166e
FDA-2008-N-0039-0059,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Sulfachlorpyridazine Powder,Rule,Final Rule,2008-06-24T04:00:00Z,2008,6,2008-06-24T04:00:00Z,,2013-07-11T14:16:03Z,E8-14291,0,0,0900006480639a99
FDA-2008-N-0039-0058,FDA,FDA-2008-N-0039,New Animal Drugs; Change of Sponsors Drug Labeler Code,Rule,Final Rule,2008-06-23T04:00:00Z,2008,6,2008-06-23T04:00:00Z,,2013-07-11T14:33:23Z,E8-14149,0,0,090000648063712a
FDA-2008-N-0039-0055,FDA,FDA-2008-N-0039,New Animal Drugs For Use in Animal Feeds; Tylosin,Rule,Final Rule,2008-06-17T04:00:00Z,2008,6,2008-06-17T04:00:00Z,,2013-07-10T18:02:55Z,E8-13606,0,0,090000648062a67e
FDA-2008-N-0039-0056,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Ivermectin Paste,Rule,Final Rule,2008-06-17T04:00:00Z,2008,6,2008-06-17T04:00:00Z,,2013-07-10T15:21:43Z,E8-13607,0,0,090000648062a642
FDA-2008-N-0039-0057,FDA,FDA-2008-N-0039,Freedom of Information Summary-Supplemental Abbreviated New Animal Drug Application-ANADA 200-326-BIMECTIN Paste 1.87% (ivermectin)-Oral Paste for use in Horses,Supporting & Related Material,Freedom of Information Summary,2008-06-17T04:00:00Z,2008,6,,,2013-07-10T15:26:02Z,,0,0,090000648062a871
FDA-2008-N-0039-0053,FDA,FDA-2008-N-0039,"Oral Dosage Form New Animal Drugs; Ivermectin, Fenbendazole, and Praziquantel Tablets",Rule,Final Rule,2008-06-13T04:00:00Z,2008,6,,,2013-07-10T16:34:56Z,E8-13354,0,0,0900006480623e54
FDA-2008-N-0039-0054,FDA,FDA-2008-N-0039,Freedom Of Information Summary NADA 141-286 Panacur Plus Chewable Dog Tablets,Supporting & Related Material,Freedom of Information Summary,2008-06-13T04:00:00Z,2008,6,,,2013-07-10T16:39:41Z,,0,0,09000064806240e3
FDA-2008-N-0039-0052,FDA,FDA-2008-N-0039,Freedom Of Information Summary - FOIS Deramaxx Chewable Tablets,Supporting & Related Material,Freedom of Information Summary,2008-06-13T04:00:00Z,2008,6,,,2013-07-10T19:10:19Z,,0,0,090000648062406b
FDA-2008-N-0039-0051,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Deracoxib,Rule,Final Rule,2008-06-13T04:00:00Z,2008,6,,,2013-07-10T19:07:16Z,E8-13353,0,0,0900006480623d7e
FDA-2008-N-0039-0050,FDA,FDA-2008-N-0039,"Freedom of Information Summary for Supplemental New Animal Drug Application - NADA 141-189, PROHEART 6 Sustained Release Injectable for Dogs (Moxidectin) Dogs over 6 months of age",Supporting & Related Material,Freedom of Information Summary,2008-06-09T04:00:00Z,2008,6,,,2013-07-10T19:18:09Z,,0,0,090000648061974d
FDA-2008-N-0039-0049,FDA,FDA-2008-N-0039,Notice of Approval of Supplemental New Animal Drug Application; Moxidectin,Rule,Approval,2008-06-09T04:00:00Z,2008,6,2008-06-09T04:00:00Z,,2013-07-10T19:13:32Z,08-01329,0,0,0900006480619532
FDA-2008-N-0039-0047,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Butorphanol,Rule,Final Rule,2008-06-02T04:00:00Z,2008,6,2008-06-02T04:00:00Z,,2013-07-10T15:16:42Z,E8-12160,0,0,090000648060bd12
FDA-2008-N-0039-0048,FDA,FDA-2008-N-0039,Freedom of Information Summary for ANADA 200-332 - BUTORPHIC Injection (butorphanol tartrate),Supporting & Related Material,Freedom of Information Summary,2008-06-02T04:00:00Z,2008,6,,,2013-07-10T15:19:46Z,,0,0,090000648060bf45
FDA-2008-N-0039-0046,FDA,FDA-2008-N-0039,Cefovecin - Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-05-22T04:00:00Z,2008,5,,,2008-05-22T16:53:54Z,,0,0,09000064805f8d0f
FDA-2008-N-0039-0045,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Cefovecin,Rule,Final Rule,2008-05-22T04:00:00Z,2008,5,2008-05-22T04:00:00Z,,2013-07-09T20:04:25Z,E8-11515,0,0,09000064805f84e3
FDA-2008-N-0039-0044,FDA,FDA-2008-N-0039,FOIS - Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-05-15T04:00:00Z,2008,5,,,2008-05-15T12:58:59Z,,0,0,09000064805c829f
FDA-2008-N-0039-0043,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Flunixin,Rule,Final Rule,2008-05-15T04:00:00Z,2008,5,2008-05-15T04:00:00Z,,2013-07-10T15:59:09Z,E8-10856,0,0,09000064805c7f71
FDA-2008-N-0039-0041,FDA,FDA-2008-N-0039,Certain Other Dosage Form New Animal Drugs; Sevoflurane,Rule,Final Rule,2008-05-07T04:00:00Z,2008,5,,,2013-07-09T18:52:23Z,E8-10153,0,0,090000648054eee0
FDA-2008-N-0039-0042,FDA,FDA-2008-N-0039,Sevoflurane; Freedom of Information Summary,Rule,Final Rule,2008-05-07T04:00:00Z,2008,5,2008-05-07T04:00:00Z,,2013-07-09T18:53:51Z,,0,0,090000648054f250
FDA-2008-N-0039-0040,FDA,FDA-2008-N-0039,New Animal Drugs; Change of Sponsors Name,Rule,Final Rule,2008-04-29T04:00:00Z,2008,4,,,2013-07-11T14:34:22Z,E8-09328,0,0,0900006480539f86
FDA-2008-N-0039-0036,FDA,FDA-2008-N-0039,New Animal Drugs; Enrofloxacin Final Rule,Rule,Final Rule,2008-04-23T04:00:00Z,2008,4,,,2013-07-10T19:23:29Z,E8-08713,0,0,090000648052275b
FDA-2008-N-0039-0038,FDA,FDA-2008-N-0039,Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-04-23T04:00:00Z,2008,4,,,2008-04-23T12:36:51Z,,0,0,0900006480511fc8
FDA-2008-N-0039-0037,FDA,FDA-2008-N-0039,Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-04-23T04:00:00Z,2008,4,,,2008-04-23T12:36:50Z,,0,0,0900006480511f87
FDA-2008-N-0039-0039,FDA,FDA-2008-N-0039,Enrofloxacin Freedom of Information Summary,Supporting & Related Material,FOIS-Freedom of Information Summary,2008-04-23T04:00:00Z,2008,4,,,2008-04-23T12:36:51Z,,0,0,0900006480522960
FDA-2008-N-0039-0035,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Insulin,Rule,Final Rule,2008-04-18T04:00:00Z,2008,4,,,2013-07-10T18:42:50Z,E8-08347,0,0,0900006480511b3a
FDA-2008-N-0039-0034,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Florfenicol,Rule,Final Rule,2008-04-18T04:00:00Z,2008,4,,,2013-07-10T19:52:36Z,E8-08346,0,0,0900006480511af1
FDA-2008-N-0039-0033,FDA,FDA-2008-N-0039,FOI Summary for NADA 141-282 ZILMAX plus RUMENSIN plus MGA (Zilpaterol Hydrochloride and Monensin USP and Melengesterol Acetate),Supporting & Related Material,Freedom of Information Summary,2008-04-10T04:00:00Z,2008,4,,,2013-07-10T17:23:56Z,,0,0,09000064804a369b
FDA-2008-N-0039-0032,FDA,FDA-2008-N-0039,New Animal Drugs For Use in Animal Feed; Zilpaterol,Rule,Final Rule,2008-04-10T04:00:00Z,2008,4,,,2013-07-10T17:18:08Z,E8-07583,0,0,09000064804a32eb
FDA-2008-N-0039-0031,FDA,FDA-2008-N-0039,"FOI Summary for ZILMAX plus RUMENSIN plus TYLAN plus MGA, NADA 141-280 (Zilpaterol Hydrochloride and Monensin USP and Tylosin Phosphate and Melengestrol Acetate)",Supporting & Related Material,Freedom of Information Summary,2008-04-08T04:00:00Z,2008,4,,,2013-07-10T17:49:51Z,,0,0,090000648046e774
FDA-2008-N-0039-0030,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feed; Zilpaterol; Technical Amendment,Rule,NFR-Notice of Final Rule,2008-04-08T04:00:00Z,2008,4,2008-04-08T04:00:00Z,,2008-04-11T22:39:13Z,E8-07307,0,0,090000648046e47e
FDA-2008-N-0039-0029,FDA,FDA-2008-N-0039,"Animal Drugs, Feeds, and Related Products; Withdrawal of Approval of NADAs; Technical Amendment",Rule,Final Rule,2008-04-04T04:00:00Z,2008,4,2008-04-04T04:00:00Z,,2013-07-11T14:36:14Z,E8-07103,0,0,0900006480439f88
FDA-2008-N-0039-0026,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Enrofloxacin,Rule,Final Rule,2008-04-02T04:00:00Z,2008,4,,,2013-07-10T19:26:20Z,E8-06706,0,0,0900006480427483
FDA-2008-N-0039-0027,FDA,FDA-2008-N-0039,"FOI Summary for Zilpaterol, NADA 141-284m ZILMAX plus MGA (Zipaterol Hydrochloride and Melengestrol Acetatate) Type A Medicated Articles",Supporting & Related Material,Freedom of Information Summary,2008-04-02T04:00:00Z,2008,4,,,2013-07-10T17:16:49Z,,0,0,090000648041496e
FDA-2008-N-0039-0028,FDA,FDA-2008-N-0039,NADA 141-068 Freedom of Information Summary,Supporting & Related Material,Freedom of Information Summary,2008-04-02T04:00:00Z,2008,4,,,2013-07-10T19:29:16Z,,0,0,09000064804276c7
FDA-2008-N-0039-0025,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Penicillin G Benzathine and Penicillin G Procaine Suspension,Rule,Final Rule,2008-03-31T04:00:00Z,2008,3,,,2013-07-11T13:26:42Z,E8-06603,0,0,0900006480414884
FDA-2008-N-0039-0024,FDA,FDA-2008-N-0039,New Animal Drugs For Use in Animal Feed; Zilpaterol,Rule,NFR-Notice of Final Rule,2008-03-31T04:00:00Z,2008,3,,,2013-07-10T16:46:30Z,E8-06601,0,0,0900006480414833
FDA-2008-N-0039-0023,FDA,FDA-2008-N-0039,FOI Summary for Nicarbazin and Bacitracin Methylene Disalycylate NADA 141-279,Supporting & Related Material,Freedom of Information Summary,2008-03-26T04:00:00Z,2008,3,,,2013-07-10T17:53:21Z,,0,0,0900006480409788
FDA-2008-N-0039-0022,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feeds; Bacitracin Methylene Disalicylate and Nicarbazin,Rule,Final Rule,2008-03-26T04:00:00Z,2008,3,,,2013-07-10T17:51:33Z,E8-06063,0,0,090000648040922b
FDA-2008-N-0039-0021,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Oxytetracycline Solution,Rule,Final Rule,2008-03-20T04:00:00Z,2008,3,,,2013-07-10T19:19:30Z,E8-05598,0,0,0900006480400974
FDA-2008-N-0039-0019,FDA,FDA-2008-N-0039,New Animal Drugs for Use in Animal Feed; Zilpaterol,Rule,Final Rule,2008-03-18T04:00:00Z,2008,3,,,2013-07-10T17:55:05Z,E8-05450,0,0,09000064803fc2e6
FDA-2008-N-0039-0018,FDA,FDA-2008-N-0039,New Animal Drugs; Change of Sponsors Name; Iron Injection; Technical Amendment,Rule,Final Rule,2008-03-18T04:00:00Z,2008,3,,,2013-07-11T12:54:27Z,E8-05452,0,0,09000064803fc3f3
FDA-2008-N-0039-0020,FDA,FDA-2008-N-0039,"Freedom of Information Summary-[NADA 141-278], ZILMAX plus RUMENSIN (Zilpaterol Hydrochloride and Monensin USP)",Supporting & Related Material,Freedom of Information Summary,2008-03-18T04:00:00Z,2008,3,,,2013-07-10T17:57:36Z,,0,0,09000064803fc63a
FDA-2008-N-0039-0017,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Penicillin G Procaine Aqueous Suspension,Rule,Final Rule,2008-03-17T04:00:00Z,2008,3,2008-03-17T04:00:00Z,,2013-07-11T13:42:23Z,E8-05217,0,0,09000064803faa5f
FDA-2008-N-0039-0016,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Change of Sponsor; Ferric Oxide Injection; Gleptoferron Injection; Iron Dextran Complex Injection; Iron Hydrogenated Dextran Injection,Rule,Final Rule,2008-03-10T04:00:00Z,2008,3,2008-03-10T04:00:00Z,,2013-07-11T14:40:49Z,E8-04603,0,0,09000064803ef1ac
FDA-2008-N-0039-0015,FDA,FDA-2008-N-0039,Intramammary Dosage Forms; Cephapirin Benzathine,Rule,Final Rule,2008-03-07T05:00:00Z,2008,3,2008-03-07T05:00:00Z,,2013-07-11T12:48:12Z,E8-04473,0,0,09000064803eace5
FDA-2008-N-0039-0013,FDA,FDA-2008-N-0039,New Animal Drugs; Albendazole,Rule,Final Rule,2008-02-29T05:00:00Z,2008,2,,,2013-07-11T12:43:54Z,E8-03877,0,0,09000064803d5031
FDA-2008-N-0039-0014,FDA,FDA-2008-N-0039,Freedom of Information Summary - [NADA-110-048-New Animal Drugs; Albendazole],Supporting & Related Material,FOIS-Freedom of Information Summary,2008-02-29T05:00:00Z,2008,2,,,2011-06-11T16:27:26Z,,0,0,09000064803d58bf
FDA-2008-N-0039-0012,FDA,FDA-2008-N-0039,Freedom of Information Summary - [ANADA-200-202-Oral Dosage Form New Animal Drugs; Ivermectin Liquid],Supporting & Related Material,Freedom of Information Summary,2008-02-22T05:00:00Z,2008,2,,,2013-07-10T15:45:54Z,,0,0,09000064803ba587
FDA-2008-N-0039-0011,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Altrenogest,Rule,Final Rule,2008-02-21T05:00:00Z,2008,2,2008-02-21T05:00:00Z,,2013-07-11T12:41:07Z,E8-03265,0,0,09000064803b9f24
FDA-2008-N-0039-0010,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Ivermectin Liquid,Rule,NFR-Notice of Final Rule,2008-02-21T05:00:00Z,2008,2,2008-02-21T05:00:00Z,,2013-07-10T15:41:57Z,E8-03266,0,0,09000064803b9f98
FDA-2008-N-0039-0009,FDA,FDA-2008-N-0039,New Animal Drugs; Change of Sponsor; Ketamine,Rule,Final Rule,2008-02-13T05:00:00Z,2008,2,2008-02-13T05:00:00Z,,2013-07-10T16:07:12Z,E8-02607,0,0,09000064803adb81
FDA-2008-N-0039-0008,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Phenylbutazone Tablets,Rule,Final Rule,2008-02-13T05:00:00Z,2008,2,2008-02-13T05:00:00Z,,2013-07-11T13:04:52Z,E8-02608,0,0,09000064803adadb
FDA-2008-N-0039-0007,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs: Spectinomycin,Rule,NFR-Notice of Final Rule,2008-02-05T05:00:00Z,2008,2,,,2008-04-11T22:39:13Z,E8-02065,0,0,09000064803a8563
FDA-2008-N-0039-0004,FDA,FDA-2008-N-0039,Freedom of Information Summary - [NADA-141-276-For Use in Animal Feed; Zilpaterol],Supporting & Related Material,Freedom of Information Summary,2008-02-01T05:00:00Z,2008,2,,,2013-07-10T18:01:23Z,,0,0,09000064803a6603
FDA-2008-N-0039-0006,FDA,FDA-2008-N-0039,Freedom of Information Summary - [NADA-141-244-Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin],Supporting & Related Material,Freedom of Information Summary,2008-02-01T05:00:00Z,2008,2,,,2013-07-10T18:37:53Z,,0,0,09000064803a66e8
FDA-2008-N-0039-0005,FDA,FDA-2008-N-0039,Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin,Rule,Final Rule,2008-02-01T05:00:00Z,2008,2,2008-02-01T05:00:00Z,,2013-07-10T18:34:59Z,E8-01906,0,0,09000064803a6488
FDA-2008-N-0039-0003,FDA,FDA-2008-N-0039,New Animal Drugs For Use in Animal Feed; Zilpaterol,Rule,Final Rule,2008-02-01T05:00:00Z,2008,2,2008-02-01T05:00:00Z,,2013-07-11T14:38:03Z,E8-01903,0,0,09000064803a642e
FDA-2008-N-0039-0002,FDA,FDA-2008-N-0039,Oral Dosage Form New Animal Drugs; Clindamycin,Rule,Final Rule,2008-01-24T05:00:00Z,2008,1,2008-01-24T05:00:00Z,,2013-07-09T20:13:31Z,E8-01199,0,0,09000064803a17e1
FDA-2008-N-0039-0001,FDA,FDA-2008-N-0039,Intramammary Dosage Forms; Cephapirin Sodium,Rule,Final Rule,2008-01-17T05:00:00Z,2008,1,2008-01-17T05:00:00Z,,2013-07-11T13:00:09Z,E8-00816,0,0,090000648039c6a6