Documents

Briefs, oral arguments, agency decisions and the Federal Register.

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  • Schedules of Controlled Substances: Temporary Placement of 4-Fluoroisobutyryl Fentanyl Into Schedule I

    Federal Register · Proposed Rule · Mar 23, 2017

    Act” or the “CSA” for the purpose of this action. … an imminent hazard to the public safety, the temporary order scheduling this substance will be effective on the date that order is published in the Federal Register , and will be in effect for a period

    82 FR 14842Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Temporary Placement of FUB-AMB Into Schedule I

    Federal Register · Proposed Rule · Sep 11, 2017

    an imminent hazard to the public safety, the temporary order scheduling this substance will be effective on the date that order is published in the Federal Register , and will be in effect for a period … 21 U.S.C. 811(h)(4), the Administrator will take into consideration any comments submitted by the Assistant Secretary with regard to the proposed temporary scheduling order.

    82 FR 42624Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Placement of Carisoprodol Into Schedule IV

    Federal Register · Rule · Dec 12, 2011

    No commenter provided such information. … 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).

    76 FR 77330Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Placement of UR-144, XLR11, and AKB48 Into Schedule I

    Federal Register · Proposed Rule · May 14, 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 27611Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Placement of AB-CHMINACA, AB-PINACA and THJ-2201 Into Schedule I

    Federal Register · Proposed Rule · Jan 27, 2017

    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.

    82 FR 8593Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Temporary Placement of U-47700 Into Schedule I

    Federal Register · Proposed Rule · Sep 7, 2016

    Act” or the “CSA” for the purpose of this action. … imminent hazard to the public safety, any subsequent final order temporarily scheduling this substance will be effective on the date of publication in the Federal Register , and will be in effect for a period

    81 FR 61636Justice DepartmentDrug Enforcement Administration
  • Control of the Immediate Precursor Norfentanyl Used in the Illicit Manufacture of Fentanyl as a Schedule II Controlled Substance

    Federal Register · Rule · Apr 17, 2020

    DEA has not identified any other legitimate uses of norfentanyl and DEA did not receive comment to the contrary during the notice and comment period of the NPRM published on September 17, 2019. 84 FR 48815 … Unfunded Mandates Reform Act of 1995 On the basis of information contained in the “Regulatory Flexibility Act” section above, DEA determined and certifies pursuant to the Unfunded Mandates Reform Act

    85 FR 21320Justice DepartmentDrug Enforcement Administration
  • Changes to and Consolidation of DEA Mailing Addresses

    Federal Register · Rule · Mar 9, 2010

    Notices regarding such renewal are published in the Federal Register, seek public comment, and provide the address to be used when submitting those comments. … 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).

    75 FR 10671Justice DepartmentDrug Enforcement Administration
  • Exempt Chemical Preparations Under the Controlled Substances Act

    Federal Register · Notice · May 20, 2026

    • Paperwork Reduction Act Comments: All comments concerning collections of information under the Paperwork Reduction Act must be submitted to the Office of Information and Regulatory Affairs, … Comments may be submitted anonymously. The Freedom of Information Act applies to all comments received.

    91 FR 29505Justice DepartmentDrug Enforcement Administration
  • Adjustment to the Aggregate Production Quota for Methylphenidate (for Sale) for 2023

    Federal Register · Notice · Oct 3, 2023

    SUPPLEMENTARY INFORMATION: Legal Authority Section 306 of the Controlled Substances Act (CSA) (21 U.S.C. 826) requires the Attorney General to establish aggregate production quotas (APQ) for each basic … DEA has determined that it is not possible to increase the APQ within the Congressionally-mandated 30-day period while also complying with the procedures that DEA previously had laid out in 21 CFR 1303.13

    88 FR 68147Justice DepartmentDrug Enforcement Administration
  • Designation of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals

    Federal Register · Rule · Apr 15, 2020

    DEA requested public comment regarding this estimate; however, no public comment was received during the notice and comment period. … Regulatory Flexibility Act The Acting Administrator, in accordance with the Regulatory Flexibility Act (5 U.S.C. 601-612), has reviewed this rule and by approving it certifies that it will not have a

    85 FR 20822Justice DepartmentDrug Enforcement Administration
  • Designation of Propionyl Chloride as a List I Chemical

    Federal Register · Rule · Mar 10, 2026

    Comment: Finally, the commenter claims that DEA's history undermines trust in its motives. … DEA requested public comments regarding this estimate, however no public comment was received during the notice and comment period regarding the costs to industry.

    91 FR 11450Justice DepartmentDrug Enforcement Administration
  • Designation of P2P Methyl Glycidic Acid as a List I Chemical

    Federal Register · Proposed Rule · Oct 2, 2025

    Commenters should be aware that the electronic Federal Docket Management System will not accept any comments after 11:59 p.m. Eastern Time on the last day of the comment period. … Comments may be submitted anonymously. The Freedom of Information Act applies to all comments received.

    90 FR 47670Justice DepartmentDrug Enforcement Administration
  • Mireille Lalanne, M.D.; Denial of Application

    Federal Register · Notice · Aug 6, 2013

    period, does not, by itself, refute the Government's prima facie case. … at 297 (Xanax is short acting and can be eliminated from the body in a relatively short period of time); id. at 242-45 (oxycodone is a medication that can result in false negative results).

    78 FR 47750Justice DepartmentDrug Enforcement Administration
  • Designation of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals

    Federal Register · Proposed Rule · Sep 13, 2019

    Commenters should be aware that the electronic Federal Docket Management System will not accept any 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 48314Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Placement of 4,4′-DMAR in Schedule I

    Federal Register · Proposed Rule · Apr 7, 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. … The Freedom of Information Act (FOIA) applies to all comments received.

    85 FR 19401Justice DepartmentDrug Enforcement Administration
  • Exemption From Import/Export Requirements for Personal Medical Use

    Federal Register · Rule · Sep 14, 2004

    Discussion of Comments DEA received two comments in response to the Notice of Proposed Rulemaking published in the Federal Register on September 11, 2003 (68 FR 53529). … One commenter disagreed with the proposed rulemaking and the other commenter supported the proposed rulemaking with additional requirements. Both commenters were individual citizens.

    69 FR 55343Justice DepartmentDrug Enforcement Administration
  • Establishment of Freight Forwarding Facilities for DEA Distributor Registrants

    Federal Register · Proposed Rule · Dec 18, 1996

    Temporary storage at the freight forwarding facility will be permitted for a period of less than twenty-four (24) hours. IV. … The records of these shipments must be maintained at the facility for a period of two years. Dated: December 6, 1996. Gene R.

    61 FR 66637Justice DepartmentDrug Enforcement Administration
  • Trinity Pharmacy II; Decision and Order

    Federal Register · Notice · Feb 20, 2018

    Under the Act, a pharmacy's registration authorizes it “to dispense,” id. … Patterson, Acting Administrator. [FR Doc. 2018-03294 Filed 2-16-18; 8:45 am] BILLING CODE 4410-09-P

    83 FR 7304Justice DepartmentDrug Enforcement Administration
  • Schedules of Controlled Substances: Temporary Placement of 10 Synthetic Cathinones Into Schedule I

    Federal Register · Rule · Mar 7, 2014

    Act” or the “CSA” for the purpose of this action. 21 U.S.C. 801-971. … The DEA has taken into consideration the Assistant Secretary's comments as required by 21 U.S.C. 811(h)(4).

    79 FR 12938Justice DepartmentDrug Enforcement Administration

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