Drug Enforcement Administration November 2020 – Federal Register Recent Federal Regulation Documents

Established Aggregate Production Quotas for Schedule I and II Controlled Substances and Assessment of Annual Needs for the List I Chemicals Ephedrine, Pseudoephedrine, and Phenylpropanolamine for 2021
Document Number: 2020-26289
Type: Notice
Date: 2020-11-30
Agency: Drug Enforcement Administration, Department of Justice
This final order establishes the initial 2021 aggregate production quotas for controlled substances in schedules I and II of the Controlled Substances Act and the assessment of annual needs for the list I chemicals ephedrine, pseudoephedrine, and phenylpropanolamine.
Importer of Controlled Substances Application: Lyndra Therapeutics
Document Number: 2020-26175
Type: Notice
Date: 2020-11-27
Agency: Drug Enforcement Administration, Department of Justice
Lyndra Therapeutics has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Importer of Controlled Substances Application: Noramco Inc.
Document Number: 2020-26174
Type: Notice
Date: 2020-11-27
Agency: Drug Enforcement Administration, Department of Justice
Noramco Inc. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Importer of Controlled Substances Application: Meridian Medical Technologies
Document Number: 2020-26172
Type: Notice
Date: 2020-11-27
Agency: Drug Enforcement Administration, Department of Justice
Meridian Medical Technologies has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Bulk Manufacturer of Controlled Substances Application: Novitium Pharma LLC
Document Number: 2020-26171
Type: Notice
Date: 2020-11-27
Agency: Drug Enforcement Administration, Department of Justice
Novitium Pharma LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Schedules of Controlled Substances: Placement of cyclopentyl fentanyl, isobutyryl fentanyl, para-chloroisobutyryl fentanyl, para-methoxybutyryl fentanyl, and valeryl fentanyl in Schedule I
Document Number: 2020-22757
Type: Rule
Date: 2020-11-25
Agency: Drug Enforcement Administration, Department of Justice
The Drug Enforcement Administration places cyclopentyl fentanyl (N-(1-phenethylpiperidin-4-yl)-N- phenylcyclopentanecarboxamide), isobutyryl fentanyl (N-(1- phenethylpiperidin-4-yl)-N-phenylisobutyramide), para-chloroisobutyryl fentanyl (N-(4-chlorophenyl)-N-(1-phenethylpiperidin-4- yl)isobutyramide), para-methoxybutyryl fentanyl (N-(4-methoxyphenyl)-N- (1-phenethylpiperidin-4-yl)butyramide), and valeryl fentanyl (N-(1- phenethylpiperidin-4-yl)-N-phenylpentanamide), including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers whenever the existence of such isomers, esters, ethers, and salts is possible, in schedule I of the Controlled Substances Act. This action continues the imposition of the regulatory controls and administrative, civil, and criminal sanctions applicable to schedule I controlled substances on persons who handle (manufacture, distribute, import, export, engage in research, conduct instructional activities or chemical analysis with, or possess), or propose to handle cyclopentyl fentanyl, isobutyryl fentanyl, para-chloroisobutyryl fentanyl, para- methoxybutyryl fentanyl, and valeryl fentanyl.
Bulk Manufacturer of Controlled Substances Application: Johnson Matthey Pharmaceutical Materials Inc.
Document Number: 2020-25764
Type: Notice
Date: 2020-11-23
Agency: Drug Enforcement Administration, Department of Justice
Johnson Matthey Pharmaceutical Materials Inc. has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Julie I. Dee, M.D.; Decision and Order
Document Number: 2020-25534
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
ECO Apothecary, LLC; Decision and Order
Document Number: 2020-25533
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Suntree Pharmacy and Suntree Medical Equipment, LLC; Decision and Order
Document Number: 2020-25531
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Monica Ferguson, F.N.P., R.N.; Decision and Order
Document Number: 2020-25529
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Jeanne E. Germeil, M.D. Decision and Order
Document Number: 2020-25528
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Hil Rizvi, M.D.; Decision and Order
Document Number: 2020-25527
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Jeffrey M. Wolk, M.D.; Decision and Order
Document Number: 2020-25526
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Jonathan Rosenfield, M.D.; Decision and Order
Document Number: 2020-25524
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Verne A. Schwager, M.D.; Decision and Order
Document Number: 2020-25523
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Lewis Leavitt III, M.D.; Decision and Order
Document Number: 2020-25521
Type: Notice
Date: 2020-11-19
Agency: Drug Enforcement Administration, Department of Justice
Bulk Manufacturer of Controlled Substances Application: Cerilliant Corporation
Document Number: 2020-24466
Type: Notice
Date: 2020-11-04
Agency: Drug Enforcement Administration, Department of Justice
Cerilliant Corporation has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
Bulk Manufacturer of Controlled Substances Application: Navinta LLC
Document Number: 2020-24465
Type: Notice
Date: 2020-11-04
Agency: Drug Enforcement Administration, Department of Justice
Navinta LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Implementation of the Substance Use-Disorder Prevention That Promotes Opioid Recovery and Treatment for Patients and Communities Act of 2018: Dispensing and Administering Controlled Substances for Medication-Assisted Treatment
Document Number: 2020-23813
Type: Rule
Date: 2020-11-02
Agency: Drug Enforcement Administration, Department of Justice
The ``Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and Communities Act of 2018 (the SUPPORT Act),'' which became law on October 24, 2018, amended the Controlled Substances Act to expand the conditions a practitioner must meet to provide medication-assisted treatment and expand the options available for a physician to be considered a qualifying physician. The SUPPORT Act removed the time period for a nurse practitioner or physician assistant to be considered a qualifying other practitioner, and revised the definition of a qualifying practitioner. The SUPPORT Act also allows a pharmacy to deliver prescribed controlled substances to a practitioner's registered location for the purpose of maintenance or detoxification treatment to be administered under certain conditions by a practitioner. The Drug Enforcement Administration amends its regulations to make them consistent with the SUPPORT Act and implement its requirements.
Suspicious Orders of Controlled Substances
Document Number: 2020-21302
Type: Proposed Rule
Date: 2020-11-02
Agency: Drug Enforcement Administration, Department of Justice
The Drug Enforcement Administration (DEA) is proposing to revise its regulations relating to suspicious orders of controlled substances, in order to implement the Preventing Drug Diversion Act of 2018 (PDDA) and to clarify the procedures a registrant must follow for orders received under suspicious circumstances (ORUSCs). Upon receipt of an ORUSC, registrants authorized to distribute controlled substances would have a choice of proceeding under one of two options (the ``two option framework''). In addition, these registrants would be required to submit all suspicious order reports to a DEA centralized database, and keep records pertaining to suspicious orders and ORUSCs.
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