83 FR 60897 - Bulk Manufacturer of Controlled Substances Registration
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 83, Issue 228 (November 27, 2018)
Drug Enforcement Administration
Federal Register Volume 83, Issue 228 (November 27, 2018)
| Page Range | 60897-60897 | |
| FR Document | 2018-25875 |
[Federal Register Volume 83, Number 228 (Tuesday, November 27, 2018)] [Notices] [Page 60897] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-25875] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Registration ACTION: Notice of registration. ----------------------------------------------------------------------- SUMMARY: The registrant listed below has applied for and been granted registration by the Drug Enforcement Administration (DEA) as bulk a manufacturer of various classes of schedule I and II controlled substances. SUPPLEMENTARY INFORMATION: The company listed below applied to be registered as bulk manufacturer of various basic classes of controlled substances. Information on the previously published notice is listed in the table below. No comments or objections were submitted for this notice. ------------------------------------------------------------------------ Company FR Docket Published ------------------------------------------------------------------------ Rhodes Technologies.......... 83 FR 40567.... August 15, 2018. ------------------------------------------------------------------------ The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of this registrant to manufacture the applicable basic classes of controlled substances is consistent with the public interest and with United States obligations under international treaties, conventions, or protocols in effect on May 1, 1971. The DEA investigated the company's maintenance of effective controls against diversion by inspecting and testing the company's physical security systems, verifying the company's compliance with state and local laws, and reviewing the company's background and history. Therefore, pursuant to 21 U.S.C. 823(a), and in accordance with 21 CFR 1301.33, the DEA has granted a registration as a bulk manufacturer to the above listed company. Dated: November 16, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2018-25875 Filed 11-26-18; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 83, No. 228 / Tuesday, November 27, 2018 / Notices 60897
Controlled substance Drug code Schedule
Remifentanil ............................................................................................................................................................. 9739 II
The company plans to import the DEPARTMENT OF JUSTICE Administration (DEA) as bulk a
above listed controlled substance for manufacturer of various classes of
research purposes. Drug Enforcement Administration schedule I and II controlled substances.
Dated: November 16, 2018. [Docket No. DEA–392] SUPPLEMENTARY INFORMATION: The
John J. Martin, company listed below applied to be
Bulk Manufacturer of Controlled registered as bulk manufacturer of
Assistant Administrator. Substances Registration
[FR Doc. 2018–25873 Filed 11–26–18; 8:45 am]
various basic classes of controlled
ACTION: Notice of registration. substances. Information on the
BILLING CODE 4410–09–P
previously published notice is listed in
SUMMARY: The registrant listed below the table below. No comments or
has applied for and been granted objections were submitted for this
registration by the Drug Enforcement notice.
Company FR Docket Published
Rhodes Technologies ............................................................. 83 FR 40567 .......................................................................... August 15, 2018.
The DEA has considered the factors in DEPARTMENT OF JUSTICE Drive, Springfield, Virginia 22152; and
21 U.S.C. 823(a) and determined that (2) Drug Enforcement Administration,
the registration of this registrant to Drug Enforcement Administration Attn: DEA Federal Register
manufacture the applicable basic classes Representative/DPW, 8701 Morrissette
[Docket No. DEA–392]
of controlled substances is consistent Drive, Springfield, Virginia 22152.
with the public interest and with United Importer of Controlled Substances SUPPLEMENTARY INFORMATION: The
States obligations under international Application: Cambridge Isotope Attorney General has delegated his
treaties, conventions, or protocols in Laboratories authority under the Controlled
effect on May 1, 1971. The DEA Substances Act to the Administrator of
investigated the company’s maintenance ACTION: Notice of application. the Drug Enforcement Administration
of effective controls against diversion by (DEA), 28 CFR 0.100(b). Authority to
inspecting and testing the company’s DATES: Registered bulk manufacturers of exercise all necessary functions with
the affected basic classes, and respect to the promulgation and
physical security systems, verifying the
applicants therefore, may file written implementation of 21 CFR part 1301,
company’s compliance with state and
comments on or objections to the incident to the registration of
local laws, and reviewing the company’s
issuance of the proposed registration on manufacturers, distributors, dispensers,
background and history. or before December 27, 2018. Such importers, and exporters of controlled
Therefore, pursuant to 21 U.S.C. persons may also file a written request substances (other than final orders in
823(a), and in accordance with 21 CFR for a hearing on the application on or connection with suspension, denial, or
1301.33, the DEA has granted a before December 27, 2018. revocation of registration) has been
registration as a bulk manufacturer to ADDRESSES: Written comments should redelegated to the Assistant
the above listed company. be sent to: Drug Enforcement Administrator of the DEA Diversion
Dated: November 16, 2018. Administration, Attention: DEA Federal Control Division (‘‘Assistant
John J. Martin,
Register Representative/DPW, 8701 Administrator’’) pursuant to section 7 of
Morrissette Drive, Springfield, Virginia 28 CFR part 0, appendix to subpart R.
Assistant Administrator. 22152. All requests for hearing must be In accordance with 21 CFR
[FR Doc. 2018–25875 Filed 11–26–18; 8:45 am] sent to: Drug Enforcement 1301.34(a), this is notice that on August
BILLING CODE 4410–09–P Administration, Attn: Administrator, 30, 2018, Cambridge Isotope
8701 Morrissette Drive, Springfield, Laboratories, 50 Frontage Road,
Virginia 22152. All requests for hearing Andover, Massachusetts 01810 applied
should also be sent to: (1) Drug to be registered as an importer of the
Enforcement Administration, Attn: following basic classes of controlled
Hearing Clerk/OALJ, 8701 Morrissette substances:
Controlled substance Drug code Schedule
Tetrahydrocannabinols ............................................................................................................................................ 7370 I
Gamma Hydroxybutyric Acid ................................................................................................................................... 2010 I
amozie on DSK3GDR082PROD with NOTICES1
Morphine .................................................................................................................................................................. 9300 II
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Document Created: 2018-11-27 01:25:31
Document Modified: 2018-11-27 01:25:31
| 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 registration. | |
| FR Citation | 83 FR 60897 |
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