82 FR 23068 - Bulk Manufacturer of Controlled Substances Application: National Center for Natural Products Research NIDA MPROJECT
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 82, Issue 96 (May 19, 2017)
Drug Enforcement Administration
Federal Register Volume 82, Issue 96 (May 19, 2017)
| Page Range | 23068-23068 | |
| FR Document | 2017-10239 |
[Federal Register Volume 82, Number 96 (Friday, May 19, 2017)] [Notices] [Page 23068] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-10239] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Application: National Center for Natural Products Research NIDA MPROJECT ACTION: Notice of application. ----------------------------------------------------------------------- DATES: Registered bulk manufacturers of the affected basic class, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before July 18, 2017. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Assistant Administrator of the DEA Diversion Control Division (``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.33(a), this is notice that on January 20, 2017, National Center for Natural Products Research NIDA MPROJECT, University of Mississippi, 135 Coy Waller Complex, P.O. Box 1848, University, Mississippi 38677-1848 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Drug code Schedule ------------------------------------------------------------------------ Marihuana Extract.................. 7350 I Marihuana.......................... 7360 I Tetrahydrocannabinols.............. 7370 I ------------------------------------------------------------------------ The company plans to bulk manufacture the listed controlled substances to make available to the National Institute on Drug Abuse (NIDA) a supply of bulk marihuana for distribution to research investigators in support of the national research program needs. No other activities for these drug codes are authorized for this registration. Dated: May 15, 2017. Louis J. Milione, Assistant Administrator. [FR Doc. 2017-10239 Filed 5-18-17; 8:45 am] BILLING CODE P
![23068 Federal Register / Vol. 82, No. 96 / Friday, May 19, 2017 / Notices
The company plans to manufacture DEPARTMENT OF JUSTICE Substances Act to the Administrator of
the listed controlled substances for the Drug Enforcement Administration
product development and reference Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to
standards. In reference to drug codes [Docket No. DEA–392] exercise all necessary functions with
7360 (marihuana) and 7370 (THC) the respect to the promulgation and
company plans to isolate these Bulk Manufacturer of Controlled implementation of 21 CFR part 1301,
controlled substances from procured Substances Application: National incident to the registration of
7350 (marihuana extract). In reference to Center for Natural Products Research manufacturers, distributors, dispensers,
drug code 7360 no cultivation activities NIDA MPROJECT importers, and exporters of controlled
are authorized for this registration. No substances (other than final orders in
ACTION: Notice of application.
other activities for these drug codes are connection with suspension, denial, or
authorized for this registration. DATES: Registered bulk manufacturers of revocation of registration) has been
the affected basic class, and applicants redelegated to the Assistant
Dated: May 15, 2017.
therefore, may file written comments on Administrator of the DEA Diversion
Louis J. Milione,
or objections to the issuance of the Control Division (‘‘Assistant
Assistant Administrator. Administrator’’) pursuant to section 7 of
proposed registration in accordance
[FR Doc. 2017–10241 Filed 5–18–17; 8:45 am] with 21 CFR 1301.33(a) on or before July 28 CFR part 0, appendix to subpart R.
BILLING CODE P 18, 2017. In accordance with 21 CFR
ADDRESSES: Written comments should 1301.33(a), this is notice that on January
be sent to: Drug Enforcement 20, 2017, National Center for Natural
Administration, Attention: DEA Federal Products Research NIDA MPROJECT,
Register Representative/DRW, 8701 University of Mississippi, 135 Coy
Morrissette Drive, Springfield, Virginia Waller Complex, P.O. Box 1848,
22152. University, Mississippi 38677–1848
SUPPLEMENTARY INFORMATION: The applied to be registered as a bulk
Attorney General has delegated his manufacturer of the following basic
authority under the Controlled classes of controlled substances:
Controlled substance Drug code Schedule
Marihuana Extract ........................................................................................................................................................... 7350 I
Marihuana ........................................................................................................................................................................ 7360 I
Tetrahydrocannabinols .................................................................................................................................................... 7370 I
The company plans to bulk DEPARTMENT OF JUSTICE authority under the Controlled
manufacture the listed controlled Substances Act to the Administrator of
substances to make available to the Drug Enforcement Administration the Drug Enforcement Administration
National Institute on Drug Abuse [Docket No. DEA–392] (DEA), 28 CFR 0.100(b). Authority to
(NIDA) a supply of bulk marihuana for exercise all necessary functions with
distribution to research investigators in Bulk Manufacturer of Controlled respect to the promulgation and
support of the national research Substances Application: Chemtos, implementation of 21 CFR part 1301,
program needs. No other activities for LLC incident to the registration of
these drug codes are authorized for this manufacturers, distributors, dispensers,
ACTION: Notice of application.
registration. importers, and exporters of controlled
Dated: May 15, 2017. DATES: Registered bulk manufacturers of substances (other than final orders in
the affected basic class, and applicants connection with suspension, denial, or
Louis J. Milione,
therefore, may file written comments on revocation of registration) has been
Assistant Administrator. redelegated to the Assistant
or objections to the issuance of the
[FR Doc. 2017–10239 Filed 5–18–17; 8:45 am] Administrator of the DEA Diversion
proposed registration in accordance
BILLING CODE P with 21 CFR 1301.33(a) on or before July Control Division (‘‘Assistant
18, 2017. Administrator’’) pursuant to section 7 of
ADDRESSES: Written comments should 28 CFR part 0, appendix to subpart R.
be sent to: Drug Enforcement In accordance with 21 CFR
Administration, Attention: DEA Federal 1301.33(a), this is notice that on July 5,
Register Representative/DRW, 8701 2016, Chemtos, LLC, 14101 W. Highway
Morrissette Drive, Springfield, Virginia 290, Building 2000B, Austin, Texas
22152. 78737–9331 applied to be registered as
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUPPLEMENTARY INFORMATION: The a bulk manufacturer for the following
Attorney General has delegated his basic classes of controlled substances:
Controlled substance Drug code Schedule
Mephedrone (4-Methyl-N-methylcathinone) .................................................................................................................... 1248 I
Methaqualone .................................................................................................................................................................. 2565 I
JWH-250 (1-Pentyl-3-(2-methoxyphenylacetyl) indole) ................................................................................................... 6250 I
5-Flouro-UR-144 and XLR11 [1-(5-Fluoro-pentyl)1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone ................. 7011 I
VerDate Sep<11>2014 19:15 May 18, 2017 Jkt 241001 PO 00000 Frm 00116 Fmt 4703 Sfmt 4703 E:\FR\FM\19MYN1.SGM 19MYN1](https://thefederalregister.org/doc/82_FR_23164/page/1.svg)
Document Created: 2018-11-08 08:47:58
Document Modified: 2018-11-08 08:47:58
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice of application. | |
| Dates | Registered bulk manufacturers of the affected basic class, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before July 18, 2017. | |
| FR Citation | 82 FR 23068 |
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