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98 rows where docket_id = "FDA-2008-N-0039" sorted by posted_date descending

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document_type 3

  • Rule 54
  • Supporting & Related Material 39
  • Notice 5

posted_year 2

  • 2008 92
  • 2009 6

agency_id 1

  • FDA 98
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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

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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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