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Briefs, oral arguments, agency decisions and the Federal Register.
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Kaniz F. Khan-Jaffery, M.D.; Decision and Order
Federal Register · Notice · Jul 29, 2020
ALJX 55 (Respondent's Letter to the Acting Administrator). … Respondent testified that when a urine test comes back clean, she would state, “Last month's urine was—didn't show any of your—any medication, why is that?
85 FR 45667Justice DepartmentDrug Enforcement AdministrationAlfred Khalily, Inc. d.b.a. Alfa Chemical; Grant of Restricted Registration
Federal Register · Notice · Jun 10, 1999
Air freight Door to Door receipts showed a transfer fee of $92.75 for the May 1994 shipment, and a transfer fee of $166.25 for the October 1994 shipment. Sky Harbor billed Respondent for these fees. … Judge Randall also concluded that ``Respondent has done nothing to assure the DEA that it will act more responsibly in future transactions.''
64 FR 31289Justice DepartmentDrug Enforcement AdministrationControlled Substances and List I Chemical Registration and Reregistration Application Fees
Federal Register · Rule · Aug 29, 2006
This Act was included in the Consolidated Appropriations Act of 2005, which was signed into law by the President on December 8, 2004 (Pub. L. 108-447). … In developing the fee schedule, DEA opted to set the fee level for a three-year period (FY 2006-2008) for two reasons.
71 FR 51105Justice DepartmentDrug Enforcement AdministrationFederal Register · Proposed Rule · Feb 21, 2019
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … The Freedom of Information Act (FOIA) applies to all comments received.
84 FR 5395Justice DepartmentDrug Enforcement AdministrationFederal Register · Rule · Nov 14, 2022
Public Comments on the NPRM DEA received four comments during the 60-day comment period. … This proposal received the most criticism during the comment period, as all commenters believe the 15-day requirement would generally be too prohibitive for registrants.
87 FR 68036Justice DepartmentDrug Enforcement AdministrationFederal Register · Proposed Rule · Nov 19, 2021
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … DEA subsequently reopened the comment period in 2020 to solicit public comment on certain issues. 85 FR 22018 (Apr. 21, 2020). 10 21 CFR 1300.03.
86 FR 64881Justice DepartmentDrug Enforcement AdministrationFederal Register · Notice · Dec 17, 2024
Issue: DEA received three comments requesting an extension of the comment period so the commenters can better research the issues and submit additional comments. … DEA Response: DEA declines to extend the comment period. The number and scope of comments indicate that the provided 30 days was adequate.
89 FR 102649Justice DepartmentDrug Enforcement AdministrationSchedules of Controlled Substances: Placement of Tramadol Into Schedule IV
Federal Register · Rule · Jul 2, 2014
a six month period. … The association stated that the ambiguity of the compliance period poses a dilemma for those in the tramadol supply chain, and requested the DEA to act to meet healthcare needs and avoid waste by allowing
79 FR 37623Justice DepartmentDrug Enforcement AdministrationRegistration and Reregistration Fees for Controlled Substance and List I Chemical Registrants
Federal Register · Proposed Rule · Mar 16, 2020
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … Additionally, the Freedom of Information Act applies to all comments received.
85 FR 14810Justice DepartmentDrug Enforcement AdministrationFederal Register · Rule · Jul 27, 2023
DEA subsequently reopened the comment period in 2020 to solicit public comment on certain issues. 85 FR 22018 (Apr. 21, 2020). 11 Medicare Program: Electronic Prescribing of Controlled Substances … Congressional Review Act This final rule is not a major rule as defined by the Congressional Review Act (CRA), 5 U.S.C. 804.
88 FR 48365Justice DepartmentDrug Enforcement AdministrationFederal Register · Rule · Jun 23, 2005
Public Comments on the NPRM DEA received six comments in response to the proposed rule. … or section 351 of the Public Health Service Act
70 FR 36338Justice DepartmentDrug Enforcement AdministrationFederal Register · Rule · Nov 2, 2020
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … Regulatory Flexibility Act The Regulatory Flexibility Act (RFA) (5 U.S.C. 601-612) applies to rules that are subject to notice and comment under section 553(b) of the APA.
85 FR 69153Justice DepartmentDrug Enforcement AdministrationControlled Substances: Adjustment to the Established 2014 Aggregate Production Quota for Marijuana
Federal Register · Notice · May 5, 2014
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after midnight Eastern Time on the last day of the comment period. … The Freedom of Information Act (FOIA) applies to all comments received.
79 FR 25620Justice DepartmentDrug Enforcement AdministrationRegistration and Reregistration Fees for Controlled Substance and List I Chemical Registrants
Federal Register · Rule · Jul 24, 2020
Act of 2005 (Pub. … Congressional Review Act This final rule is a major rule as defined by the Congressional Review Act, 5 U.S.C. 804.
85 FR 44710Justice DepartmentDrug Enforcement AdministrationImplementation of the Methamphetamine Production Prevention Act of 2008
Federal Register · Proposed Rule · Mar 23, 2010
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after midnight Eastern Time on the last day of the comment period. … ability to submit comments at midnight Eastern time on the day the comment period closes.
75 FR 13702Justice DepartmentDrug Enforcement AdministrationSchedules of Controlled Substances: Placement of Carisoprodol Into Schedule IV
Federal Register · Proposed Rule · Nov 17, 2009
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after midnight Eastern Standard Time (EST) on the last day of the comment period. … to submit comments at midnight EST on the day the comment period closes.
74 FR 59108Justice DepartmentDrug Enforcement AdministrationSchedules of Controlled Substances: Placement of Lasmiditan in Schedule V
Federal Register · Rule · May 24, 2021
Both commenters urged DEA to consider placing lasmiditan in schedule IV for a probationary or provisional time period with the option to reclassify lasmiditan as a schedule V substance. … Regulatory Flexibility Act The Regulatory Flexibility Act (RFA) (5 U.S.C. 601-612) applies to rules that are subject to notice and comment under section 553(b) of the APA.
86 FR 27803Justice DepartmentDrug Enforcement AdministrationSchedules of Controlled Substances: Placement of Eluxadoline Into Schedule IV
Federal Register · Proposed Rule · Aug 11, 2015
Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … The Freedom of Information Act (FOIA) applies to all comments received.
80 FR 48044Justice DepartmentDrug Enforcement AdministrationRegistration Requirements for Individual Practitioners Operating in a “Locum Tenens” Capacity
Federal Register · Proposed Rule · Oct 28, 2009
ability to submit comments at midnight Eastern Time on the day the comment period closes. … Please note that the Freedom of Information Act applies to all comments received.
74 FR 55499Justice DepartmentDrug Enforcement AdministrationInformation on Foreign Chain of Distribution for Ephedrine, Pseudoephedrine, and Phenylpropanolamine
Federal Register · Proposed Rule · Mar 31, 2008
Imports handled by the foreign distributor may not be restricted during the 60-day period. … Congressional Review Act This rule is not a major rule as defined by section 804 of the Small Business Regulatory Enforcement Fairness Act of 1996 (Congressional Review Act).
73 FR 16793Justice DepartmentDrug Enforcement Administration
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