Notice2022-26925
Importer of Controlled Substances Application: VHG Labs dba LGC Standards
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
December 12, 2022
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
VHG Labs dba LGC Standards has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Full Text
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<title>Federal Register, Volume 87 Issue 237 (Monday, December 12, 2022)</title>
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[Federal Register Volume 87, Number 237 (Monday, December 12, 2022)]
[Notices]
[Pages 76084-76086]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2022-26925]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1114]
Importer of Controlled Substances Application: VHG Labs dba LGC
Standards
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: VHG Labs dba LGC Standards has applied to be registered as an
importer of basic class(es) of controlled substance(s). Refer to
SUPPLEMENTARY INFORMATION listed below for further drug information.
DATES: Registered bulk manufacturers of the affected basic class(es),
and applicants therefore, may submit electronic comments on or
objections to the issuance of the proposed registration on or before
January 11, 2023. Such persons may also file a written request for a
hearing on the application on or before January 11, 2023.
ADDRESSES: The Drug Enforcement Administration requires that all
comments be submitted electronically through the Federal eRulemaking
Portal, which provides the ability to type short comments directly into
the comment field on the web page or attach a file for lengthier
comments. Please go to <a href="https://www.regulations.gov">https://www.regulations.gov</a> and follow the
online instructions at that site for submitting comments. Upon
submission of your comment, you will receive a Comment Tracking Number.
Please be aware that submitted comments are not instantaneously
available for public view on <a href="https://www.regulations.gov">https://www.regulations.gov</a>. If you have
received a Comment Tracking Number, your comment has been successfully
submitted and there is no need to resubmit the same comment. All
requests for a hearing must 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. All requests for a hearing should also be
sent to: Drug Enforcement Administration, Attn: Administrator, 8701
Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this
is notice that on September 12, 2022, VHG Labs dba LGC Standards, 3
Perimeter Road, Manchester, New Hampshire 03103-3341, applied to be
registered as an importer of the following basic class(es) of
controlled substance(s):
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Controlled substance Drug code Schedule
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Cathinone........................... 1235 I
Methcathinone....................... 1237 I
[[Page 76085]]
Mephedrone (4-Methyl-N- 1248 I
methylcathinone).
Naphyrone........................... 1258 I
N-Ethylamphetamine.................. 1475 I
Gamma Hydroxybutyric Acid........... 2010 I
Methaqualone........................ 2565 I
JWH-250 (1-Pentyl-3-(2- 6250 I
methoxyphenylacetyl) indole).
SR-18 (Also known as RCS-8) (1- 7008 I
Cyclohexylethyl-3-(2-
methoxyphenylacetyl) indole).
APINACA and AKB48 N-(1-Adamantyl)-1- 7048 I
pentyl-1H-indazole-3-carboxamide.
JWH-081 (1-Pentyl-3-(1-(4- 7081 I
methoxynaphthoyl) indole).
SR-19 (Also known as RCS-4) (1- 7104 I
Pentyl-3-[(4-methoxy)-benzoyl]
indole.
JWH-018 (also known as AM678) (1- 7118 I
Pentyl-3-(1-naphthoyl)indole).
JWH-122 (1-Pentyl-3-(4-methyl-1- 7122 I
naphthoyl) indole).
UR-144 (1-Pentyl-1H-indol-3- 7144 I
yl)(2,2,3,3-
tetramethylcyclopropyl)methanone.
JWH-203 (1-Pentyl-3-(2- 7203 I
chlorophenylacetyl) indole).
Ibogaine............................ 7260 I
Lysergic acid diethylamide.......... 7315 I
Marihuana Extract................... 7350 I
Marihuana........................... 7360 I
Tetrahydrocannabinols............... 7370 I
Mescaline........................... 7381 I
2,5-Dimethoxyamphetamine............ 7396 I
JWH-398 (1-Pentyl-3-(4-chloro-1- 7398 I
naphthoyl) indole).
3,4-Methylenedioxymethamphetamine... 7405 I
4-Methoxyamphetamine................ 7411 I
5-Methoxy-N-N-dimethyltryptamine.... 7431 I
Bufotenine.......................... 7433 I
Psilocybin.......................... 7437 I
Psilocyn............................ 7438 I
4-Methyl- 7498 I
alphapyrrolidinopropiophenone (4-
MePPP).
MDPV (3,4- 7535 I
Methylenedioxypyrovalerone).
Methylone (3,4-Methylenedioxy-N- 7540 I
methylcathinone).
Butylone............................ 7541 I
Pentylone........................... 7542 I
Codeine-N-oxide..................... 9053 I
Desomorphine........................ 9055 I
Dihydromorphine..................... 9145 I
Heroin.............................. 9200 I
Morphine-N-oxide.................... 9307 I
Normorphine......................... 9313 I
Pholcodine.......................... 9314 I
Alphamethadol....................... 9605 I
Norlevorphano....................... 9634 I
Properidine......................... 9644 I
Tilidine............................ 9750 I
Alpha-methylfentanyl................ 9814 I
Acetyl Fentanyl (N-(1- 9821 I
phenethylpiperidin-4-yl)-N-
phenylacetamide).
Butyryl Fentany..................... 9822 I
Fentanyl-related substance.......... 9850 I
Amphetamine......................... 1100 II
Methamphetamine..................... 1105 II
Phenmetrazine....................... 1631 II
Methylphenidate..................... 1724 II
Amobarbital......................... 2125 II
Pentobarbital....................... 2270 II
Secobarbital........................ 2315 II
Glutethimide........................ 2550 II
Phencyclidine....................... 7471 II
4-Anilino-N-phenethyl-4-piperidine 8333 II
(ANPP).
Norfentanyl......................... 8366 II
Phenylacetone....................... 8501 II
Cocaine............................. 9041 II
Codeine............................. 9050 II
Dihydrocodeine...................... 9120 II
Oxycodone........................... 9143 II
Hydromorphone....................... 9150 II
Diphenoxylate....................... 9170 II
Ecgonine............................ 9180 II
Ethylmorphine....................... 9190 II
Hydrocodone......................... 9193 II
Levorphanol......................... 9220 II
Isomethadone........................ 9226 II
Meperidine.......................... 9230 II
Meperidine intermediate-A........... 9232 II
Meperidine intermediate-B........... 9233 II
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Meperidine intermediate-C........... 9234 II
Methadone........................... 9250 II
Methadone intermediate.............. 9254 II
Dextropropoxyphene, bulk (non-dosage 9273 II
forms).
Morphine............................ 9300 II
Thebaine............................ 9333 II
Oxymorphone......................... 9652 II
14-Hydroxmorphone................... 9665 II
Noroxymorphone...................... 9668 II
Phenazocine......................... 9715 II
Sufentanil.......................... 9740 II
Carfentanil......................... 9743 II
Fentanyl............................ 9801 II
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The company plans to import the listed controlled substances for
sale to research facilities for drug testing and analysis. In reference
to drug codes 7360 (Marihuana) and 7370 (Tetrahydrocannabinols) the
company plans to import a synthetic cannabidiol and a synthetic
tetrahydrocannabinol. No other activities for these drug codes are
authorized for this registration.
Approval of permit applications will occur only when the
registrant's business activity is consistent with what is authorized
under 21 U.S.C. 952(a)(2). Authorization will not extend to the import
of Food and Drug Administration-approved or non-approved finished
dosage forms for commercial sale.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2022-26925 Filed 12-9-22; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on December 12, 2022.
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