{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\", document_type = \"Proposed Rule\" and posted_year = 2013 sorted by posted_date descending", "rows": [["FDA-1979-N-0409-0001", "FDA", "FDA-1979-N-0409", "Blood and Blood Components; Error and Accident Reports - Notice of Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-31T05:00:00Z", 2013, 12, "2013-12-31T05:00:00Z", "1980-11-07T04:59:59Z", "2014-05-08T14:18:07Z", null, 0, 0, "090000648055636a"], ["FDA-1979-N-0307-0001", "FDA", "FDA-1979-N-0307", "Allergenic Products; Proposed Testing and Labeling Requirements; Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-30T05:00:00Z", 2013, 12, "2013-12-30T05:00:00Z", "1980-07-02T03:59:59Z", "2014-06-18T16:36:34Z", null, 0, 0, "090000648055517f"], ["FDA-1979-N-0309-0001", "FDA", "FDA-1979-N-0309", "Additional Standards for Human Blood Products; Antihemophillic Factor (Human) - Notice of Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-30T05:00:00Z", 2013, 12, "2013-12-30T05:00:00Z", null, "2014-05-13T14:33:51Z", null, 0, 0, "090000648055519b"], ["FDA-1979-N-0084-0001", "FDA", "FDA-1979-N-0084", "Food Labeling; Net Weight Labeling Requirements - Notice of Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-30T05:00:00Z", 2013, 12, "2013-12-30T05:00:00Z", "1980-11-07T04:59:59Z", "2014-05-12T18:31:25Z", null, 0, 0, "0900006480553e82"], ["FDA-1980-N-0149-0001", "FDA", "FDA-1980-N-0149", "Withdrawal of Certain Pre-1986 Proposed Rules - Notice of Proposed Rulemaking", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-30T05:00:00Z", 2013, 12, "2013-12-30T05:00:00Z", null, "2014-05-08T12:45:51Z", null, 0, 0, "09000064805bcf5d"], ["FDA-2013-N-0500-0006", "FDA", "FDA-2013-N-0500", "Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products; Correction and Extension of Comment Period", "Proposed Rule", "Extension of Comment Period", "2013-12-27T05:00:00Z", 2013, 12, "2013-12-27T05:00:00Z", "2014-03-14T03:59:59Z", "2014-04-10T01:02:03Z", "2013-30881", 0, 0, "09000064814debad"], ["FDA-2013-N-1563-0001", "FDA", "FDA-2013-N-1563", "Appendix 4 to Draft Qualitative Risk Assessment of Risk of Activity/Food\nCombinations for Activities (Outside the Farm Definition) Conducted in a\nFacility Co-Located on a Farm; Availability", "Proposed Rule", "Request for Comment", "2013-12-24T05:00:00Z", 2013, 12, "2013-12-24T05:00:00Z", "2014-04-01T03:59:59Z", "2014-01-01T02:04:13Z", "2013-30375", 0, 0, "09000064814d536f"], ["FDA-2013-N-1425-0001", "FDA", "FDA-2013-N-1425", "Focused Mitigation Strategies To Protect Food Against Intentional\nAdulteration; Public Meeting on Proposed Rule", "Proposed Rule", "Public Meeting", "2013-12-24T05:00:00Z", 2013, 12, "2013-12-24T05:00:00Z", null, "2013-12-24T15:38:06Z", "2013-30372", 0, 0, "09000064814d54bf"], ["FDA-2013-N-1425-0002", "FDA", "FDA-2013-N-1425", "Focused Mitigation Strategies to Protect Food Against Intentional Adulteration", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-24T05:00:00Z", 2013, 12, "2013-12-24T05:00:00Z", "2014-04-01T03:59:59Z", "2014-04-04T01:02:32Z", "2013-30373", 0, 0, "09000064814d53fc"], ["FDA-2013-F-1540-0001", "FDA", "FDA-2013-F-1540", "Food Additive Petitions; Animal Use: DSM Nutritional Products", "Proposed Rule", "Petition", "2013-12-23T05:00:00Z", 2013, 12, "2013-12-23T05:00:00Z", "2014-01-23T04:59:59Z", "2014-01-14T19:58:32Z", "2013-30461", 0, 0, "09000064814d2f4a"], ["FDA-2013-F-1539-0001", "FDA", "FDA-2013-F-1539", "DSM Nutritional Products; Filing of Food Additive Petition (Animal Use)", "Proposed Rule", "Petition", "2013-12-23T05:00:00Z", 2013, 12, "2013-12-23T05:00:00Z", "2014-01-23T04:59:59Z", "2024-11-07T23:01:24Z", "2013-30462", 1, 0, "09000064814d308c"], ["FDA-1975-N-0012-0317", "FDA", "FDA-1975-N-0012", "Safety and Effectiveness of Consumer Antiseptics; Topical Antimicrobial\nDrug Products for Over-the-Counter Human Use; Proposed Amendment of the Tentative Final Monograph; Reopening of Administrative Record", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-12-17T05:00:00Z", 2013, 12, "2013-12-17T05:00:00Z", "2015-02-17T04:59:59Z", "2018-02-16T22:20:40Z", "2013-29814", 0, 0, "09000064814c4d8a"], ["FDA-2010-N-0155-0139", "FDA", "FDA-2010-N-0155", "Veterinary Feed Directive", "Proposed Rule", "Advance Notice of Proposed Rulemaking (ANPRM)", "2013-12-12T05:00:00Z", 2013, 12, "2013-12-12T05:00:00Z", "2014-03-13T03:59:59Z", "2015-06-02T16:57:20Z", "2013-29696", 0, 0, "09000064814ba038"], ["FDA-2013-N-1523-0001", "FDA", "FDA-2013-N-1523", "Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act; Request for Nominations", "Proposed Rule", "Request for Information", "2013-12-04T05:00:00Z", 2013, 12, "2013-12-04T05:00:00Z", "2014-03-05T04:59:59Z", "2014-03-11T01:02:11Z", "2013-28980", 0, 0, "09000064814a61e6"], ["FDA-2013-N-1525-0001", "FDA", "FDA-2013-N-1525", "List of Bulk Drug Substances That May Be Used in Pharmacy Compounding; Bulk Drug Substances That May Be Used To Compound Drug Products in Accordance With Section 503A of the Federal Food, Drug, and Cosmetic Act", "Proposed Rule", "Withdrawal", "2013-12-04T05:00:00Z", 2013, 12, "2013-12-04T05:00:00Z", "2014-03-05T04:59:59Z", "2014-10-03T01:02:26Z", "2013-28979", 0, 0, "09000064814a631f"], ["FDA-2013-N-1524-0001", "FDA", "FDA-2013-N-1524", "Bulk Drug Substances that May be Used to Compound Drug Products, etc., Concerning Outsourcing Facilities: Request for Nominations", "Proposed Rule", "Request for Information", "2013-12-04T05:00:00Z", 2013, 12, "2013-12-04T05:00:00Z", "2014-03-05T04:59:59Z", "2017-07-19T01:02:39Z", "2013-28978", 0, 0, "09000064814a6122"], ["FDA-2013-N-0001-0109", "FDA", "FDA-2013-N-0001", "Medical Gas Regulation Review Meeting; Correction", "Proposed Rule", "Public Meeting", "2013-11-25T05:00:00Z", 2013, 11, "2013-11-25T05:00:00Z", null, "2013-11-26T13:29:50Z", "2013-28083", 0, 0, "09000064814959de"], ["FDA-2011-N-0143-0037", "FDA", "FDA-2011-N-0143", "Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-11-20T05:00:00Z", 2013, 11, "2013-11-20T05:00:00Z", "2014-01-28T04:59:59Z", "2014-11-12T15:25:38Z", "2013-27645", 0, 0, "090000648148b9c5"], ["FDA-2011-N-0146-0039", "FDA", "FDA-2011-N-0146", "Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-11-20T05:00:00Z", 2013, 11, "2013-11-20T05:00:00Z", "2014-01-28T04:59:59Z", "2014-11-12T15:25:43Z", "2013-27644", 0, 0, "090000648148bc0e"], ["FDA-2011-N-0920-0288", "FDA", "FDA-2011-N-0920", "Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-11-20T05:00:00Z", 2013, 11, "2013-11-20T05:00:00Z", "2013-11-23T04:59:59Z", "2015-04-17T02:02:04Z", "2013-27783", 0, 0, "090000648148b9c3"], ["FDA-2012-S-0782-0014", "FDA", "FDA-2012-S-0782", "See  Docket ID FDA-2011-N-0921 for the Correct Federal Register Document for Comment Participation", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-11-20T05:00:00Z", 2013, 11, "2013-11-20T05:00:00Z", "2013-11-23T04:59:59Z", "2015-10-19T20:06:56Z", "2013-27784", 0, 0, "090000648148bc43"], ["FDA-2011-N-0921-0321", "FDA", "FDA-2011-N-0921", "Environmental Impact Statement for the Proposed Rule: Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Comment Period", "Proposed Rule", "Extension of Comment Period", "2013-11-18T05:00:00Z", 2013, 11, "2013-11-18T05:00:00Z", "2014-03-16T03:59:59Z", "2014-04-16T01:02:36Z", "2013-27479", 0, 0, "0900006481486c94"], ["FDA-2013-N-0500-0001", "FDA", "FDA-2013-N-0500", "Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-11-13T05:00:00Z", 2013, 11, "2013-11-13T05:00:00Z", "2014-01-14T04:59:59Z", "2016-04-26T19:00:32Z", "2013-26799", 0, 0, "090000648147a982"], ["FDA-2012-S-0782-0013", "FDA", "FDA-2012-S-0782", "See  Docket ID FDA-2013-N-0501 for the Correct Federal Register Document for Comment Participation", "Proposed Rule", "Request for Comment", "2013-11-13T05:00:00Z", 2013, 11, "2013-11-13T05:00:00Z", "2014-01-14T04:59:59Z", "2024-11-12T05:24:30Z", null, 1, 0, "090000648147a7d5"], ["FDA-2011-N-0898-0015", "FDA", "FDA-2011-N-0898", "Permanent Discontinuance or Interruption in Manufacturing of Certain Drug or Biological Products", "Proposed Rule", "Request for Comment", "2013-11-04T05:00:00Z", 2013, 11, "2013-11-04T05:00:00Z", "2014-01-04T04:59:59Z", "2014-08-29T01:04:25Z", "2013-25956", 0, 0, "090000648146f1a4"], ["FDA-2013-N-0001-0102", "FDA", "FDA-2013-N-0001", "Medical Gas Regulation Review; Announcement of Public Meeting", "Proposed Rule", "Public Meeting", "2013-11-01T04:00:00Z", 2013, 11, "2013-11-01T04:00:00Z", null, "2013-11-01T15:09:59Z", "2013-26056", 0, 0, "090000648146bfde"], ["FDA-2011-N-0922-0001", "FDA", "FDA-2011-N-0922", "Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals; Public Meeting on Proposed Rule", "Proposed Rule", "Public Meeting", "2013-10-29T04:00:00Z", 2013, 10, "2013-10-29T04:00:00Z", null, "2013-11-03T00:00:58Z", "2013-25125", 0, 0, "090000648146529f"], ["FDA-2013-N-1043-0001", "FDA", "FDA-2013-N-1043", "Draft Qualitative Risk Assessment of Risk of Activity/Animal Food Combinations for Activities (Outside the Farm Definition) Conducted in a Facility Co-Located on a Farm; Availability", "Proposed Rule", "Request for Comment", "2013-10-29T04:00:00Z", 2013, 10, "2013-10-29T04:00:00Z", "2014-02-27T04:59:59Z", "2024-11-12T05:22:42Z", "2013-25124", 1, 0, "0900006481464b4c"], ["FDA-2011-N-0922-0002", "FDA", "FDA-2011-N-0922", "Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-10-29T04:00:00Z", 2013, 10, "2013-11-01T04:00:00Z", "2014-02-27T04:59:59Z", "2015-01-28T13:39:04Z", "2013-25126", 0, 0, "0900006481466af9"], ["FDA-2012-S-0782-0002", "FDA", "FDA-2012-S-0782", "See  Docket ID FDA-2011-N-0922- for the Correct Federal Register Document for Comment Participation", "Proposed Rule", null, "2013-10-29T00:00:00Z", 2013, 10, null, null, "2022-04-21T14:11:13Z", null, 0, 1, "09000064814651d4"], ["FDA-2012-N-0447-0028", "FDA", "FDA-2012-N-0447", "Antimicrobial Animal Drug Sales and Distribution Annual Summary Report Data Tables", "Proposed Rule", "Request for Comment", "2013-09-26T04:00:00Z", 2013, 9, "2013-09-26T04:00:00Z", "2013-11-26T04:59:59Z", "2014-01-14T16:24:26Z", "2013-23488", 0, 0, "090000648143b90d"], ["FDA-2011-N-0143-0028", "FDA", "FDA-2011-N-0143", "Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meetings", "Proposed Rule", "Public Meeting", "2013-09-18T04:00:00Z", 2013, 9, "2013-09-18T04:00:00Z", null, "2014-02-05T14:07:48Z", "2013-22655", 0, 0, "0900006481429d03"], ["FDA-2011-N-0146-0030", "FDA", "FDA-2011-N-0146", "Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meetings", "Proposed Rule", "Public Meeting", "2013-09-18T04:00:00Z", 2013, 9, "2013-09-18T04:00:00Z", null, "2013-09-18T14:57:00Z", "2013-22655", 0, 0, "090000648142a07f"], ["FDA-2013-C-1008-0001", "FDA", "FDA-2013-C-1008", "Wm. Wrigley Jr. Company; Filing of Color Additive Petition", "Proposed Rule", "Petition", "2013-09-17T04:00:00Z", 2013, 9, "2013-09-17T04:00:00Z", null, "2013-09-17T15:14:29Z", "2013-22522", 0, 0, "090000648142765f"], ["FDA-2013-N-0521-0079", "FDA", "FDA-2013-N-0521", "Menthol in Cigarettes, Tobacco Products; Request for Comments; Extension of Comment Period", "Proposed Rule", "Advance Notice of Proposed Rulemaking (ANPRM)", "2013-09-11T04:00:00Z", 2013, 9, "2013-09-11T04:00:00Z", "2013-11-23T04:59:59Z", "2014-10-04T01:07:43Z", "2013-22015", 0, 0, "09000064813f31ff"], ["FDA-2011-N-0921-0204", "FDA", "FDA-2011-N-0921", "Notice of Intent to Prepare an Environmental Impact Statement for the Proposed Rule, Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-08-19T04:00:00Z", 2013, 8, "2013-08-19T04:00:00Z", "2013-11-16T04:59:59Z", "2014-05-25T00:06:34Z", "2013-20087", 0, 0, "09000064813b8a9c"], ["FDA-2013-N-0888-0001", "FDA", "FDA-2013-N-0888", "Dean Foods Company and WhiteWave Foods Company; Filing of Food Additive Petition", "Proposed Rule", "Petition", "2013-08-16T04:00:00Z", 2013, 8, "2013-08-16T04:00:00Z", null, "2013-08-16T13:33:11Z", "2013-19915", 0, 0, "09000064813b58ec"], ["FDA-2011-N-0146-0027", "FDA", "FDA-2011-N-0146", "Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meeting", "Proposed Rule", "Public Meeting", "2013-08-16T04:00:00Z", 2013, 8, "2013-08-16T04:00:00Z", null, "2013-09-04T18:04:49Z", "2013-19961", 0, 0, "09000064813b5836"], ["FDA-2011-N-0143-0025", "FDA", "FDA-2011-N-0143", "Food and Drug Administration Food Safety Modernization Act:  Proposed Rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies; Public Meeting", "Proposed Rule", "Public Meeting", "2013-08-16T04:00:00Z", 2013, 8, "2013-08-16T04:00:00Z", "2014-01-28T04:59:59Z", "2014-02-06T02:05:17Z", "2013-19961", 0, 0, "09000064813b5f99"], ["FDA-1977-N-0421-0001", "FDA", "FDA-1977-N-0421", "New Drugs for Investigational Use Availability of Draft of Bioresearch Monitoring Data Collection Form - Notice of Proposed Rulemaking", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-08-12T04:00:00Z", 2013, 8, "2013-08-12T04:00:00Z", null, "2013-08-13T12:26:29Z", null, 0, 0, "09000064805ef588"], ["FDA-1977-N-0162-0001", "FDA", "FDA-1977-N-0162", "Drugs for Human and Veterinary Use Public Disclosure of Specifications - Notice of Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-08-12T04:00:00Z", 2013, 8, "2013-08-12T04:00:00Z", "1977-09-14T03:59:59Z", "2013-08-13T01:01:41Z", null, 0, 0, "09000064805db106"], ["FDA-2011-N-0921-0199", "FDA", "FDA-2011-N-0921", "Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-08-09T04:00:00Z", 2013, 8, "2013-08-09T04:00:00Z", "2013-11-23T04:59:59Z", "2015-04-15T02:01:08Z", "2013-19302", 0, 0, "09000064813a84a8"], ["FDA-2011-N-0920-0188", "FDA", "FDA-2011-N-0920", "Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-08-09T04:00:00Z", 2013, 8, "2013-08-09T04:00:00Z", "2013-11-23T04:59:59Z", "2014-11-21T03:02:32Z", "2013-19300", 0, 0, "09000064813a8674"], ["FDA-2011-N-0146-0024", "FDA", "FDA-2011-N-0146", "Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-07-29T04:00:00Z", 2013, 7, "2013-07-29T04:00:00Z", "2013-11-27T04:59:59Z", "2014-09-13T01:06:47Z", "2013-17994", 0, 0, "09000064813823a9"], ["FDA-2011-N-0143-0023", "FDA", "FDA-2011-N-0143", "Foreign Supplier Verification Programs for Importers of Food for Humans and Animals", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-07-29T04:00:00Z", 2013, 7, "2013-07-29T04:00:00Z", "2013-11-27T04:59:59Z", "2014-07-01T01:02:50Z", "2013-17993", 0, 0, "090000648138252e"], ["FDA-2013-N-0639-0002", "FDA", "FDA-2013-N-0639", "Turtles Intrastate and Interstate Requirements; 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Theuer; Filing of Food Additive Petition and Citizen Petition", "Proposed Rule", "Petition", "2013-07-19T04:00:00Z", 2013, 7, "2013-07-19T04:00:00Z", null, "2013-07-19T19:15:31Z", "2013-17330", 0, 0, "090000648137061b"], ["FDA-1998-C-0381-0001", "FDA", "FDA-1998-C-0381", "Sensient Technologies Corporation; Withdrawal of Color Additive Petition", "Proposed Rule", "Withdrawal", "2013-07-19T04:00:00Z", 2013, 7, "2013-07-19T04:00:00Z", null, "2013-07-19T18:59:13Z", "2013-17382", 0, 0, "0900006481370520"], ["FDA-2013-N-0365-0003", "FDA", "FDA-2013-N-0365", "Administrative Detention of Drugs Intended for Human or Animal Use", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-07-15T04:00:00Z", 2013, 7, "2013-07-15T04:00:00Z", "2013-09-14T03:59:59Z", "2013-09-20T19:31:48Z", "2013-16843", 0, 0, "09000064813667d8"], ["FDA-1990-N-0172-0001", "FDA", "FDA-1990-N-0172", "Food Labeling; Reference Daily Intakes and Daily Reference Values - Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-07-11T04:00:00Z", 2013, 7, "1990-07-19T04:00:00Z", "1990-11-17T04:59:59Z", "2015-04-25T21:55:33Z", null, 0, 0, "090000648052dbee"], ["FDA-2013-N-0568-0002", "FDA", "FDA-2013-N-0568", "Physical Medicine Devices; Reclassification of Stair-Climbing Wheelchairs; Correction", "Proposed Rule", "Correction", "2013-07-02T04:00:00Z", 2013, 7, "2013-07-02T04:00:00Z", "2013-09-11T03:59:59Z", "2014-01-14T13:49:53Z", "2013-15789", 0, 0, "09000064813515e5"], ["FDA-2012-N-0303-0003", "FDA", "FDA-2012-N-0303", "Gastroenterology-Urology Devices; Reclassification of Implanted Blood Access Devices", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-06-28T04:00:00Z", 2013, 6, "2013-06-28T04:00:00Z", "2013-07-30T03:59:59Z", "2014-01-14T13:32:34Z", "2013-15504", 0, 0, "0900006481348988"], ["FDA-2011-N-0070-0001", "FDA", "FDA-2011-N-0070", "Laser Products; Proposed Amendment to Performance Standard", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-06-24T04:00:00Z", 2013, 6, "2013-06-24T04:00:00Z", "2013-09-24T03:59:59Z", "2014-01-14T13:55:12Z", "2013-14846", 0, 0, "090000648133b662"], ["FDA-2013-N-0684-0001", "FDA", "FDA-2013-N-0684", "Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments", "Proposed Rule", "Public Meeting", "2013-06-20T04:00:00Z", 2013, 6, "2013-06-20T04:00:00Z", "2013-08-13T03:59:59Z", "2014-01-14T13:35:39Z", "2013-14549", 0, 0, "0900006481333a7d"], ["FDA-2013-N-0685-0001", "FDA", "FDA-2013-N-0685", "Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments", "Proposed Rule", "Public Meeting", "2013-06-20T04:00:00Z", 2013, 6, "2013-06-20T04:00:00Z", "2013-08-13T03:59:59Z", "2014-01-14T13:37:38Z", "2013-14549", 0, 0, "0900006481333a7e"], ["FDA-2013-N-0581-0001", "FDA", "FDA-2013-N-0581", "Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary Syndrome, Cardiac and Non-Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for IABP for Other Specific Intended Uses", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-06-19T04:00:00Z", 2013, 6, "2013-06-19T04:00:00Z", "2013-09-18T03:59:59Z", "2014-01-14T13:53:46Z", "2013-14553", 0, 0, "0900006481331179"], ["FDA-2013-N-0683-0001", "FDA", "FDA-2013-N-0683", "Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments", "Proposed Rule", "Public Meeting", 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Administration Safety and Innovation Act", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-06-12T04:00:00Z", 2013, 6, "2013-06-12T04:00:00Z", "2013-08-13T03:59:59Z", "2014-01-14T13:36:59Z", "2013-13865", 0, 0, "090000648131adbc"], ["FDA-2012-N-0920-0001", "FDA", "FDA-2012-N-0920", "Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-05-31T04:00:00Z", 2013, 5, "2013-05-31T04:00:00Z", "2013-08-15T03:59:59Z", "2014-07-10T13:46:56Z", "2013-12927", 0, 0, "0900006481304148"], ["FDA-2013-N-0487-0001", "FDA", "FDA-2013-N-0487", "Cardiovascular Devices; Reclassification of External Counter-Pulsating Devices for Treatment of Chronic Stable Angina; Effective Date of Requirement for Premarket Approval for External Counter-Pulsating Devices for Other Specified Intended Uses", "Proposed Rule", "Notice of Proposed 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Food; Extension of Comment Periods", "Proposed Rule", "Extension of Comment Period", "2013-04-26T04:00:00Z", 2013, 4, "2013-04-26T04:00:00Z", "2013-08-09T03:59:59Z", "2013-08-12T01:02:35Z", "2013-09763", 0, 0, "09000064812a946e"], ["FDA-2012-N-1258-0003", "FDA", "FDA-2012-N-1258", "Draft Qualitative Risk Assessment of Risk of Activity/Food Combinations for Activities (Outside the Farm Definition) Conducted in Facility Co-Located on Farm; Availability: Extension of Comment Period", "Proposed Rule", "Extension of Comment Period", "2013-04-26T04:00:00Z", 2013, 4, "2013-04-26T04:00:00Z", "2013-09-17T03:59:59Z", "2013-09-17T01:02:45Z", "2013-09762", 0, 0, "09000064812a94a4"], ["FDA-2011-N-0921-0087", "FDA", "FDA-2011-N-0921", "Standards for Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: Extension of comment periods", "Proposed Rule", "Extension of Comment Period", "2013-04-26T04:00:00Z", 2013, 4, "2013-04-26T04:00:00Z", "2013-08-09T03:59:59Z", "2013-10-01T01:01:59Z", "2013-09761", 0, 0, "09000064812a94a8"], ["FDA-2013-N-0125-0001", "FDA", "FDA-2013-N-0125", "Use of Certain Symbols in Labeling", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-04-19T04:00:00Z", 2013, 4, "2013-04-19T04:00:00Z", "2013-06-19T03:59:59Z", "2013-06-25T01:28:35Z", "2013-09175", 0, 0, "090000648129c6c1"], ["FDA-2013-N-0067-0001", "FDA", "FDA-2013-N-0067", "Infant Formula: The Addition of Minimum and Maximum Levels of Selenium to Infant Formula and Related Labeling Requirements", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-04-16T04:00:00Z", 2013, 4, "2013-04-16T04:00:00Z", "2013-07-02T03:59:59Z", "2013-07-02T01:02:24Z", "2013-08855", 0, 0, "0900006481295cad"], ["FDA-2013-N-0365-0001", "FDA", "FDA-2013-N-0365", "Administrative Detention under the Food and Drug Administration Safety and Innovation Act", "Proposed Rule", "Request for Comment", "2013-04-09T04:00:00Z", 2013, 4, "2013-04-09T04:00:00Z", "2013-05-10T03:59:59Z", "2013-09-20T19:30:59Z", "2013-08120", 0, 0, "0900006481289e68"], ["FDA-2013-N-0195-0001", "FDA", "FDA-2013-N-0195", "Effective Date of Requirement for Premarket Approval for Three Class III Preamendments Devices: Reclassification of Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2013-04-04T04:00:00Z", 2013, 4, "2013-04-04T04:00:00Z", "2013-05-07T03:59:59Z", "2014-05-07T01:03:54Z", "2013-07730", 0, 0, "0900006481268b15"], ["FDA-2012-S-0782-0006", "FDA", "FDA-2012-S-0782", "See  Document ID FDA-2013-D-0269-0001 for the Correct Federal Register Document for Comment Participation", "Proposed Rule", "GDL Guidance", "2013-03-26T04:00:00Z", 2013, 3, "2013-03-26T04:00:00Z", "2013-05-29T03:59:59Z", "2015-10-19T20:13:38Z", "2013-06824", 0, 0, "090000648124521d"], ["FDA-2013-N-0234-0001", "FDA", "FDA-2013-N-0234", "Effective Dates of Requirements for Premarket Approvals: Automated 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