Federal Register - March 1, 2021

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Fuente: Federal Register

12033

Federal Register / Vol. 86, No. 38 / Monday, March 1, 2021 / Notices Groff NA Hemplex, LLC has applied to be registered as an importer of basic classes of controlled substances. Refer to Supplemental Information listed below for further drug information.

SUMMARY:

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 March 31, 2021. Such persons may also file a written request for a hearing on the application on or before March 31, 2021.

DATES:

Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing should also be sent to: 1 Drug Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and 2 Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152.

ADDRESSES:

In accordance with 21 CFR 1301.34a, this is notice that on January 19, 2021, Groff NA Hemplex, LLC, 100 Redco Avenue, Suite A, Red Lion, Pennsylvania 17356
1436, applied to be registered as an importer of the following basic classes of controlled substances:

SUPPLEMENTARY INFORMATION:

Drug code
Controlled substance Marihuana Extract
Marihuana
Tetrahydrocannabinols

7350
7360
7370

Schedule I
I I

The company plans to import finished dosage unit products containing Marihuana Extracts for clinical trial studies. These Marihuana Extracts compounds are listed under drug code 7350. No other activity for this drug code is authorized for this registration.
Approval of permit applications will occur only when the registrants business activity is consistent with what is authorized under 21 U.S.C. 952a2.
Authorization will not extend to the import of Food and Drug Administration-approved or nonapproved finished dosage forms for commercial sale.
William T. McDermott, Assistant Administrator.
FR Doc. 202104181 Filed 22621; 8:45 am BILLING CODE 441009P

DEPARTMENT OF JUSTICE
Drug Enforcement Administration Docket No. DEA799

Importer of Controlled Substances Application: Microgenics Corporation Thermo Fisher Scientific Drug Enforcement Administration, Justice.
ACTION: Notice of application.
AGENCY:

Microgenics Corporation Thermo Fisher Scientific has applied to
SUMMARY:

be registered as an importer of basic classes of controlled substances.
Refer to Supplemental Information listed below for further drug information.
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 March 31, 2021. Such persons may also file a written request for a hearing on the application on or before March 31, 2021.

DATES:

Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All request for a hearing should also be sent to: 1 Drug Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and 2 Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152.

ADDRESSES:

In accordance with 21 CFR 1301.34a, this is notice that on January 27, 2021, Microgenics Corporation Thermo Fisher Scientific, 46500 Kato Road Fremont, California 94538, has applied to be registered as an importer of the following basic classes of controlled substances:

SUPPLEMENTARY INFORMATION:

Controlled substance
Drug code
Cathinone
Mephedrone 4-Methyl-N-methylcathinone
Gamma Hydroxybutyric Acid
Methaqualone
Mecloqualone
2-1-4-fluorobenzyl-1Hindazole-3-carboxamido-3-methylbutanoate
ABPINACA N-1-amino-3-methyl-1-oxobutan-2-yl-1-pentyl-1H-indazole-3-carboxamide
ABCHMINACA N-1-amino-3-methyl-1-oxobutan-2-yl-1-cyclohexylmethyl-1H-indazole-3-carboxamide
MABCHMINACA N-1-amino-3,3dimethyl-1-oxobutan-2-yl-1-cyclohexylmethyl-1H-indazole-3-carboxamide
5FAMB Methyl 2-1-5-fluoropentyl-1H-indazole-3-carboxamido-3-methylbutanoate
ADBPINACA N-1-amino-3,3-dimethyl-1-oxobutan-2-yl-1-pentyl-1H-indazole-3-carboxamide
APINACA and AKB48 N-1-Adamantyl-1-pentyl-1H-indazole-3-carboxamide
AM2201 1-5-Fluoropentyl-3-1-naphthoyl indole
Lysergic acid diethylamide
Marihuana
Tetrahydrocannabinols
3,4-Methylenedioxyamphetamine
3,4-Methylenedioxy-N-ethylamphetamine
3,4-Methylenedioxymethamphetamine
2-4-iodo-2,5-dimethoxyphenyl ethanamine 2CI
MDPV 3,4-Methylenedioxypyrovalerone
2-4-iodo-2,5-dimethoxyphenyl-N-2-methoxybenzyl ethanamine 25INBOMe
Butylone
Pentylone
alpha-pyrrolidinopentiophenone a-PVP
Normorphine

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2010
2565
2572
7021
7023
7031
7032
7033
7035
7048
7201
7315
7360
7370
7400
7404
7405
7518
7535
7538
7541
7542
7545
9313

Schedule I
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I I
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Federal Register - March 1, 2021

TítuloFederal Register

PaísEstados Unidos de América

Fecha01/03/2021

Nro. de páginas242

Nro. de ediciones7798

Primera edición14/03/1936

Ultima edición18/06/2026

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