80 FR 52511 - Manufacturer of Controlled Substances Registration: Johnson Matthey Pharmaceutical Materials, Inc.
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 80, Issue 168 (August 31, 2015)
Drug Enforcement Administration
Federal Register Volume 80, Issue 168 (August 31, 2015)
| Page Range | 52511-52511 | |
| FR Document | 2015-21521 |
[Federal Register Volume 80, Number 168 (Monday, August 31, 2015)] [Notices] [Page 52511] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2015-21521] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Manufacturer of Controlled Substances Registration: Johnson Matthey Pharmaceutical Materials, Inc. ACTION: Notice of registration. ----------------------------------------------------------------------- SUMMARY: Johnson Matthey Pharmaceutical Materials, Inc. applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Johnson Matthey Pharmaceutical Materials, Inc. registration as a manufacturer of those controlled substances. SUPPLEMENTARY INFORMATION: By notice dated April 14, 2015, and published in the Federal Register on April 22, 2015, 80 FR 22559, Johnson Matthey Pharmaceutical Materials, Inc., 25 Patton Road, Devens, Massachusetts 01434 applied to be registered as a manufacturer of certain basic classes of controlled substances. No comments or objections were submitted for this notice. The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Johnson Matthey Pharmaceutical Materials, Inc. to manufacture the 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 above-named company is granted registration as a bulk manufacturer of the basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Schedule ------------------------------------------------------------------------ Amphetamine (1100)......................... II Methylphenidate (1724)..................... II Nabilone (7379)............................ II Hydrocodone (9193)......................... II Alfentanil (9737).......................... II Remifentanil (9739)........................ II Sufentanil (9740).......................... II ------------------------------------------------------------------------ The company plans to utilize this facility to manufacture small quantities of the listed controlled substances in bulk and to conduct analytical testing in support of the company's primary manufacturing facility in West Deptford, New Jersey. The controlled substances manufactured in bulk at this facility will be distributed to its company's customers. Dated: August 21, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015-21521 Filed 8-28-15; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 80, No. 168 / Monday, August 31, 2015 / Notices 52511
DATES: Registered bulk manufacturers of Dated: August 21, 2015. Controlled substance Schedule
the affected basic classes, and Joseph T. Rannazzisi,
applicants therefore, may file written Deputy Assistant Administrator. Remifentanil (9739) ...................... II
comments on or objections to the [FR Doc. 2015–21557 Filed 8–28–15; 8:45 am]
Sufentanil (9740) .......................... II
issuance of the proposed registration in BILLING CODE 4410–09–P
accordance with 21 CFR 1301.34(a) on The company plans to utilize this
or before September 30, 2015. Such facility to manufacture small quantities
persons may also file a written request DEPARTMENT OF JUSTICE of the listed controlled substances in
for a hearing on the application bulk and to conduct analytical testing in
pursuant to 21 CFR 1301.43 on or before Drug Enforcement Administration support of the company’s primary
September 30, 2015. manufacturing facility in West Deptford,
[Docket No. DEA–392] New Jersey. The controlled substances
ADDRESSES: Written comments should manufactured in bulk at this facility will
be sent to: Drug Enforcement Manufacturer of Controlled
be distributed to its company’s
Administration, Attention: DEA Federal Substances Registration: Johnson
customers.
Register Representative/ODXL, 8701 Matthey Pharmaceutical Materials, Inc.
Dated: August 21, 2015.
Morrissette Drive, Springfield, Virginia ACTION: Notice of registration. Joseph T. Rannazzisi,
22152. Request for hearings should be
Deputy Assistant Administrator.
sent to: Drug Enforcement SUMMARY: Johnson Matthey
[FR Doc. 2015–21521 Filed 8–28–15; 8:45 am]
Administration, Attention: Hearing Pharmaceutical Materials, Inc. applied
Clerk/LJ, 8701 Morrissette Drive, BILLING CODE 4410–09–P
to be registered as a manufacturer of
Springfield, Virginia 22152. Comments certain basic classes of controlled
and request for hearings on applications substances. The Drug Enforcement
DEPARTMENT OF JUSTICE
to import narcotic raw material are not Administration (DEA) grants Johnson
appropriate. 72 FR 3417 (January 25, Matthey Pharmaceutical Materials, Inc. Drug Enforcement Administration
2007). registration as a manufacturer of those
controlled substances. [Docket No. DEA–392]
SUPPLEMENTARY INFORMATION: The
SUPPLEMENTARY INFORMATION: By notice Bulk Manufacturer of Controlled
Attorney General has delegated her
dated April 14, 2015, and published in Substances Application: Rhodes
authority under the Controlled
the Federal Register on April 22, 2015, Technologies
Substances Act to the Administrator of 80 FR 22559, Johnson Matthey
the Drug Enforcement Administration Pharmaceutical Materials, Inc., 25 ACTION: Notice of application.
(DEA), 28 CFR 0.100(b). Authority to Patton Road, Devens, Massachusetts
exercise all necessary functions with 01434 applied to be registered as a DATES: Registered bulk manufacturers of
respect to the promulgation and manufacturer of certain basic classes of the affected basic classes, and
implementation of 21 CFR part 1301, controlled substances. No comments or applicants therefore, may file written
incident to the registration of objections were submitted for this comments on or objections to the
manufacturers, distributors, dispensers, notice. issuance of the proposed registration in
importers, and exporters of controlled The DEA has considered the factors in accordance with 21 CFR 1301.33(a) on
substances (other than final orders in 21 U.S.C. 823(a) and determined that or before October 30, 2015.
connection with suspension, denial, or the registration of Johnson Matthey ADDRESSES: Written comments should
revocation of registration) has been Pharmaceutical Materials, Inc. to be sent to: Drug Enforcement
redelegated to the Deputy Assistant manufacture the basic classes of Administration, Attention: DEA Federal
Administrator of the DEA Office of controlled substances is consistent with Register Representative/ODXL, 8701
Diversion Control (‘‘Deputy Assistant the public interest and with United Morrissette Drive, Springfield, Virginia
Administrator’’) pursuant to section 7 of States obligations under international 22152. Request for hearings should be
28 CFR part 0, appendix to subpart R. treaties, conventions, or protocols in sent to: Drug Enforcement
In accordance with 21 CFR effect on May 1, 1971. The DEA Administration, Attention: Hearing
1301.34(a), this is notice that on June 3, investigated the company’s maintenance Clerk/LJ, 8701 Morrissette Drive,
2015, Cambrex Charles City, 1205 11th of effective controls against diversion by Springfield, Virginia 22152.
Street, Charles City, Iowa 50616–3466 inspecting and testing the company’s SUPPLEMENTARY INFORMATION: The
applied to be registered as an importer physical security systems, verifying the Attorney General has delegated her
of the following basic classes of company’s compliance with state and authority under the Controlled
controlled substances: local laws, and reviewing the company’s Substances Act to the Administrator of
background and history. the Drug Enforcement Administration
Therefore, pursuant to 21 U.S.C. (DEA), 28 CFR 0.100(b). Authority to
Controlled substance Schedule 823(a), and in accordance with 21 CFR exercise all necessary functions with
1301.33, the above-named company is respect to the promulgation and
4-Anilino-N-phenethyl-4-piperidine II granted registration as a bulk implementation of 21 CFR part 1301,
(8333). manufacturer of the basic classes of incident to the registration of
Phenylacetone (8501) .................. II controlled substances: manufacturers, distributors, dispensers,
Opium, raw (9600) ....................... II
tkelley on DSK3SPTVN1PROD with NOTICES
importers, and exporters of controlled
Poppy Straw Concentrate (9670) II Controlled substance Schedule substances (other than final orders in
Amphetamine (1100) .................... II
connection with suspension, denial, or
The company plans to import the Methylphenidate (1724) ................ II revocation of registration) has been
listed controlled substances for internal Nabilone (7379) ............................ II redelegated to the Deputy Assistant
use, and to manufacture bulk Hydrocodone (9193) ..................... II Administrator of the DEA Office of
intermediates for sale to its customers. Alfentanil (9737) ........................... II Diversion Control (‘‘Deputy Assistant
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Document Created: 2018-02-23 11:04:27
Document Modified: 2018-02-23 11:04:27
| 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 | 80 FR 52511 |
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