83 FR 4685 - Bulk Manufacturer of Controlled Substances Registration
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 83, Issue 22 (February 1, 2018)
Drug Enforcement Administration
Federal Register Volume 83, Issue 22 (February 1, 2018)
| Page Range | 4685-4685 | |
| FR Document | 2018-02007 |
[Federal Register Volume 83, Number 22 (Thursday, February 1, 2018)] [Notices] [Page 4685] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-02007] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Registration ACTION: Notice of registration. ----------------------------------------------------------------------- SUMMARY: Registrants listed below have applied for and been granted registration by the Drug Enforcement Administration as bulk manufacturers of various classes of schedule I and II controlled substances. SUPPLEMENTARY INFORMATION: The companies listed below applied to be registered as bulk manufacturers of various basic classes of controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted for these notices. ---------------------------------------------------------------------------------------------------------------- Company FR Docket Published ---------------------------------------------------------------------------------------------------------------- Euticals, Inc............................ 82 FR 50159 October 30, 2017. Cerilliant Corporation................... 82 FR 51439 November 6, 2017. Cambrex Charles City..................... 82 FR 51642 November 7, 2017. ---------------------------------------------------------------------------------------------------------------- The Drug Enforcement Administration (DEA) has considered the factors in 21 U.S.C. 823(a) and determined that the registration of these registrants 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 each of the company's maintenance of effective controls against diversion by inspecting and testing each company's physical security systems, verifying each company's compliance with state and local laws, and reviewing each 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 persons. Dated: January 26, 2018. Susan A. Gibson, Deputy Assistant Administrator. [FR Doc. 2018-02007 Filed 1-31-18; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 83, No. 22 / Thursday, February 1, 2018 / Notices 4685
submit to the Commission on or before Commission in connection with these Issued: January 26, 2018.
February 22, 2018, a written brief investigations must certify that the Lisa R. Barton,
containing information and arguments information is accurate and complete to Secretary to the Commission.
pertinent to the subject matter of the the best of the submitter’s knowledge. In [FR Doc. 2018–01965 Filed 1–31–18; 8:45 am]
investigations. Parties may file written making the certification, the submitter BILLING CODE 7020–02–P
testimony in connection with their will acknowledge that any information
presentation at the conference. All that it submits to the Commission
written submissions must conform with during these investigations may be
the provisions of section 201.8 of the DEPARTMENT OF JUSTICE
disclosed to and used: (i) By the
Commission’s rules; any submissions Commission, its employees and Offices, Drug Enforcement Administration
that contain BPI must also conform with and contract personnel (a) for
the requirements of sections 201.6, developing or maintaining the records
[Docket No. DEA–392]
207.3, and 207.7 of the Commission’s
of these or related investigations or Bulk Manufacturer of Controlled
rules. The Commission’s Handbook on
reviews, or (b) in internal investigations, Substances Registration
E-Filing, available on the Commission’s
website at https://edis.usitc.gov, audits, reviews, and evaluations relating
elaborates upon the Commission’s rules to the programs, personnel, and ACTION: Notice of registration.
with respect to electronic filing. operations of the Commission including
under 5 U.S.C. Appendix 3; or (ii) by SUMMARY: Registrants listed below have
In accordance with sections 201.16(c) applied for and been granted
U.S. government employees and
and 207.3 of the rules, each document registration by the Drug Enforcement
contract personnel, solely for
filed by a party to the investigations Administration as bulk manufacturers of
must be served on all other parties to cybersecurity purposes. All contract
various classes of schedule I and II
the investigations (as identified by personnel will sign appropriate controlled substances.
either the public or BPI service list), and nondisclosure agreements.
SUPPLEMENTARY INFORMATION: The
a certificate of service must be timely Authority: These investigations are being companies listed below applied to be
filed. The Secretary will not accept a conducted under authority of title VII of the registered as bulk manufacturers of
document for filing without a certificate Tariff Act of 1930; this notice is published various basic classes of controlled
of service. pursuant to section 207.12 of the substances. Information on previously
Certification.—Pursuant to section Commission’s rules. published notices is listed in the table
207.3 of the Commission’s rules, any By order of the Commission. below. No comments or objections were
person submitting information to the submitted for these notices.
Company FR Docket Published
Euticals, Inc .................................................................................................................................................. 82 FR 50159 October 30, 2017.
Cerilliant Corporation .................................................................................................................................... 82 FR 51439 November 6, 2017.
Cambrex Charles City .................................................................................................................................. 82 FR 51642 November 7, 2017.
The Drug Enforcement 1301.33, the DEA has granted a SUMMARY: Registrants listed below have
Administration (DEA) has considered registration as a bulk manufacturer to applied for and been granted
the factors in 21 U.S.C. 823(a) and the above listed persons. registration by the Drug Enforcement
determined that the registration of these Dated: January 26, 2018. Administration as importers of various
registrants to manufacture the Susan A. Gibson, classes of schedule I or II controlled
applicable basic classes of controlled substances.
Deputy Assistant Administrator.
substances is consistent with the public
interest and with United States [FR Doc. 2018–02007 Filed 1–31–18; 8:45 am] SUPPLEMENTARY INFORMATION: The
obligations under international treaties, BILLING CODE 4410–09–P companies listed below applied to be
conventions, or protocols in effect on registered as importers of various basic
May 1, 1971. The DEA investigated each classes of controlled substances.
of the company’s maintenance of DEPARTMENT OF JUSTICE
Information on previously published
effective controls against diversion by Drug Enforcement Administration notices is listed in the table below. No
inspecting and testing each company’s comments or objections were submitted
physical security systems, verifying [Docket No. DEA–392]
and no requests for hearing were
each company’s compliance with state submitted for these notices.
and local laws, and reviewing each Importer of Controlled Substances
company’s background and history. Registration
Therefore, pursuant to 21 U.S.C.
ACTION: Notice of registration.
823(a), and in accordance with 21 CFR
Company FR Docket Published
sradovich on DSK3GMQ082PROD with NOTICES
ABBVIE, LTD ................................................................................................................................................. 82 FR 56994 December 1, 2017.
VHG Labs DBA LGC Standard Warehouse ................................................................................................. 82 FR 58654 December 13, 2017.
The Drug Enforcement the factors in 21 U.S.C. 823, 952(a) and registration of the listed registrants to
Administration (DEA) has considered 958(a) and determined that the import the applicable basic classes of
VerDate Sep<11>2014 19:34 Jan 31, 2018 Jkt 244001 PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 E:\FR\FM\01FEN1.SGM 01FEN1](https://thefederalregister.org/doc/83_FR_4707/page/1.svg)
Document Created: 2018-10-26 13:47:11
Document Modified: 2018-10-26 13:47:11
| 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 4685 |
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