Federal Register - February 24, 2021

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Source: Federal Register

11330

Federal Register / Vol. 86, No. 35 / Wednesday, February 24, 2021 / Notices Controlled substance
Drug code
Codeine
Ecgonine
Levorphanol
Meperidine
Methadone
Morphine
Thebaine
Levo-Alphacetylmethadol LAAM
Noroxymorphone
Remifentanil
Sufentanil
Carfentanil
Fentanyl

The company plans to manufacture reference standards.
William T. McDermott, Assistant Administrator.
FR Doc. 202103760 Filed 22321; 8:45 am BILLING CODE 441009P

DEPARTMENT OF JUSTICE
Drug Enforcement Administration Docket No. DEA796

Bulk Manufacturer of Controlled Substances Application: Bulk Manufacturer of Marihuana: Livwell Michigan, LLC
Drug Enforcement Administration, Justice.
ACTION: Notice of application.
AGENCY:

The Drug Enforcement Administration DEA is providing notice of an application it has received from an entity applying to be registered to manufacture in bulk basic classes of controlled substances listed in schedule I. DEA intends to evaluate this and other pending applications according to its regulations governing the program of growing marihuana for scientific and medical research under DEA
registration.
DATES: Registered bulk manufacturers of the affected basic classes, and applicants therefor, may file written comments on or objections to the issuance of the proposed registration on or before April 26, 2021.
ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW 8701
Morrissette Drive, Springfield, Virginia 22152. To ensure proper handling of comments, please reference Docket No.
DEA796 in all correspondence, including attachments.
SUPPLEMENTARY INFORMATION: The Controlled Substances Act CSA
prohibits the cultivation and
khammond on DSKJM1Z7X2PROD with NOTICES

SUMMARY:

VerDate Sep<11>2014

17:21 Feb 23, 2021

Jkt 253001

distribution of marihuana except by persons who are registered under the CSA to do so for lawful purposes. In accordance with the purposes specified in 21 CFR 1301.33a, DEA is providing notice that the entity identified below has applied for registration as a bulk manufacturer of schedule I controlled substances. In response, registered bulk manufacturers of the affected basic classes, and applicants therefor, may file written comments on or objections of the requested registration, as provided in this notice. This notice does not constitute any evaluation or determination of the merits of the application submitted.
The applicant plans to manufacture bulk active pharmaceutical ingredients APIs for product development and distribution to DEA-registered researchers. If the application for registration is granted, the registrant would not be authorized to conduct other activity under this registration aside from those coincident activities specifically authorized by DEA
regulations. DEA will evaluate the application for registration as a bulk manufacturer for compliance with all applicable laws, treaties, and regulations and to ensure adequate safeguards against diversion are in place.
As this applicant has applied to become registered as a bulk manufacturer of marihuana, the application will be evaluated under the criteria of 21 U.S.C. 823a. DEA will conduct this evaluation in the manner described in the rule published at 85 FR
82333 on December 18, 2020, and reflected in DEA regulations at 21 CFR
part 1318.
In accordance with 21 CFR
1301.33a, DEA is providing notice that on January 25, 2021, Livwell Michigan, LLC, 21550 Hoover Road, Warren, Michigan 48089, applied to be registered as a bulk manufacturer of the following basic classes of controlled substances:

PO 00000

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Controlled substance Marihuana Extract
Marihuana
Tetrahydrocannabinols

9050
9180
9220
9230
9250
9300
9333
9648
9668
9739
9740
9743
9801

Schedule II
II
II
II
II
II
II
II
II
II
II
II
II

Drug code 7350
7360
7370

Schedule I
I I

William T. McDermott, Assistant Administrator.
FR Doc. 202103759 Filed 22321; 8:45 am BILLING CODE 441009P

DEPARTMENT OF JUSTICE
Drug Enforcement Administration Docket No. DEA792

Bulk Manufacturer of Controlled Substances Application: Synthcon LLC
Drug Enforcement Administration, Justice.
ACTION: Notice of application.
AGENCY:

Synthcon LLC, has applied to be registered as a bulk manufacturer of basic classes of controlled substances. Refer to Supplemental Information listed below for further drug information.
DATES: Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before April 26, 2021. Such persons may also file a written request for a hearing on the application on or before April 26, 2021.
ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33a, this is notice that on January 5, 2021, Synthcon LLC., 770 Wooten Road, Suite 101, Colorado Springs, Colorado 80915
3538, applied to be registered as a bulk SUMMARY:

E:FRFM24FEN1.SGM

24FEN1

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Federal Register - February 24, 2021

TitoloFederal Register

PaeseStati Uniti

Data24/02/2021

Conteggio pagine308

Numero di edizioni7802

Prima edizione14/03/1936

Ultima edizione25/06/2026

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