81 FR 30343 - Importer of Controlled Substances Registration: Siegfried USA, LLC
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 81, Issue 94 (May 16, 2016)
Drug Enforcement Administration
Federal Register Volume 81, Issue 94 (May 16, 2016)
| Page Range | 30343-30344 | |
| FR Document | 2016-11414 |
[Federal Register Volume 81, Number 94 (Monday, May 16, 2016)] [Notices] [Pages 30343-30344] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-11414] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Importer of Controlled Substances Registration: Siegfried USA, LLC ACTION: Notice of registration. ----------------------------------------------------------------------- [[Page 30344]] SUMMARY: Siegfried USA, LLC applied to be registered as an importer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Siegfried USA, LLC registration as an importer of those controlled substances. SUPPLEMENTARY INFORMATION: By notice dated January 11, 2016, and published in the Federal Register on January 19, 2016, 81 FR 2910, Siegfried USA, LLC, 33 Industrial Park Road, Pennsville, New Jersey 08070 applied to be registered as an importer of certain basic classes of controlled substances. Comments and requests for hearings on applications to import narcotic raw material are not appropriate. 72 FR 3417, (January 25, 2007). The DEA has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of Siegfried USA, LLC to import 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. 952(a) and 958(a), and in accordance with 21 CFR 1301.34, the above-named company is granted registration as an importer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Schedule ------------------------------------------------------------------------ Opium, raw (9600).......................... II Poppy Straw Concentrate (9670)............. II ------------------------------------------------------------------------ The company plans to import the listed controlled substances to manufacture bulk active pharmaceutical ingredients (API) for distribution to its customer. Dated: April 28, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016-11414 Filed 5-13-16; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 81, No. 94 / Monday, May 16, 2016 / Notices 30343
accordance with section 210.13 of the manufacture the basic classes of published in the Federal Register on
Commission’s Rules of Practice and controlled substances is consistent with December 8, 2015, 80 FR 76311,
Procedure, 19 CFR 210.13. Pursuant to the public interest and with United Johnson Matthey Pharmaceutical
19 CFR 201.16(e) and 210.13(a), such States obligations under international Materials, Inc., 25 Patton Road, Devens,
responses will be considered by the treaties, conventions, or protocols in Massachusetts 01434 applied to be
Commission if received not later than 20 effect on May 1, 1971. The DEA registered as a manufacturer of certain
days after the date of service by the investigated the company’s maintenance basic classes of controlled substances.
Commission of the complaint and the of effective controls against diversion by No comments or objections were
notice of investigation. Extensions of inspecting and testing the company’s submitted for this notice.
time for submitting responses to the physical security systems, verifying the The DEA has considered the factors in
complaint and the notice of company’s compliance with state and 21 U.S.C. 823(a) and determined that
investigation will not be granted unless local laws, and reviewing the company’s the registration of Johnson Matthey
good cause therefor is shown. background and history. Pharmaceutical Materials, Inc. to
Failure of a respondent to file a timely Therefore, pursuant to 21 U.S.C. manufacture the basic classes of
response to each allegation in the 823(a), and in accordance with 21 CFR controlled substances is consistent with
complaint and in this notice may be 1301.33, the above-named company is the public interest and with United
deemed to constitute a waiver of the granted registration as a bulk States obligations under international
right to appear and contest the manufacturer of the following basic treaties, conventions, or protocols in
allegations of the complaint and this classes of controlled substances: effect on May 1, 1971. The DEA
notice, and to authorize the investigated the company’s maintenance
administrative law judge and the Controlled substance Schedule of effective controls against diversion by
Commission, without further notice to inspecting and testing the company’s
Gamma Hydroxybutyric Acid I
the respondent, to find the facts to be as (2010). physical security systems, verifying the
alleged in the complaint and this notice Marihuana (7360) ......................... I company’s compliance with state and
and to enter an initial determination Tetrahydrocannabinols (7370) ..... I local laws, and reviewing the company’s
and a final determination containing Psilocybin (7437) .......................... I background and history.
such findings, and may result in the Psilocyn (7438) ............................. I Therefore, pursuant to 21 U.S.C.
issuance of an exclusion order or a cease Heroin (9200) ............................... I 823(a), and in accordance with 21 CFR
and desist order or both directed against Lysergic acid diethylamide (7315) II
Morphine (9300) ........................... II 1301.33, the above-named company is
the respondent. granted registration as a bulk
By order of the Commission. The company plans to manufacture manufacturer of the following basic
Issued: May 11, 2016. reference standards for distribution to classes of controlled substances:
Lisa R. Barton, its research and forensics customers. In
reference to drug codes 7360 Controlled substance Schedule
Secretary to the Commission.
[FR Doc. 2016–11448 Filed 5–13–16; 8:45 am] (marihuana) and 7370 (THC) the Amphetamine (1100) .................... II
BILLING CODE 7020–02–P company plans to manufacture these Methylphenidate (1724) ................ II
drugs as synthetic. No other activities Nabilone (7379) ............................ II
for these drug codes are authorized for Hydrocodone (9193) ..................... II
DEPARTMENT OF JUSTICE this registration. Alfentanil (9737) ........................... II
Remifentanil (9739) ...................... II
Dated: May 9, 2016.
Drug Enforcement Administration Sufentanil (9740) .......................... II
Louis J. Milione,
[Docket No. DEA–392] Deputy Assistant Administrator. The company plans to utilize this
[FR Doc. 2016–11393 Filed 5–13–16; 8:45 am] facility to manufacture small quantities
Manufacturer of Controlled BILLING CODE 4410–09–P of the listed controlled substances in
Substances Registration: Organix, Inc. bulk and to conduct analytical testing in
ACTION: Notice of registration. support of the company’s primary
DEPARTMENT OF JUSTICE manufacturing facility in West Deptford,
SUMMARY: Organix, Inc. applied to be New Jersey. The controlled substances
Drug Enforcement Administration
registered as a manufacturer of certain manufactured in bulk at this facility will
basic classes of controlled substances. [Docket No. DEA–392] be distributed to its customers.
The Drug Enforcement Administration Dated: May 9, 2016.
(DEA) grants Organix, Inc. registration Manufacturer of Controlled
Substances Registration: Johnson Louis J. Milione,
as a manufacturer of those controlled
Matthey Pharmaceutical Materials, Inc. Deputy Assistant Administrator.
substances.
[FR Doc. 2016–11394 Filed 5–13–16; 8:45 am]
SUPPLEMENTARY INFORMATION: By notice ACTION: Notice of registration. BILLING CODE 4410–09–P
dated November 27, 2015, and
published in the Federal Register on SUMMARY: Johnson Matthey
December 3, 2015, 80 FR 75691, Pharmaceutical Materials, Inc. applied
DEPARTMENT OF JUSTICE
Organix, Inc., 240 Salem Street, to be registered as a manufacturer of
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Woburn, Massachusetts 01801 applied certain basic classes of controlled Drug Enforcement Administration
to be registered as a manufacturer of substances. The Drug Enforcement
certain basic classes of controlled Administration (DEA) grants Johnson [Docket No. DEA–392]
substances. No comments or objections Matthey Pharmaceutical Materials, Inc.
were submitted for this notice. registration as a manufacturer of those Importer of Controlled Substances
The DEA has considered the factors in controlled substances. Registration: Siegfried USA, LLC
21 U.S.C. 823(a) and determined that SUPPLEMENTARY INFORMATION: By notice
ACTION: Notice of registration.
the registration of Organix, Inc. to dated November 30, 2015, and
VerDate Sep<11>2014 18:48 May 13, 2016 Jkt 238001 PO 00000 Frm 00107 Fmt 4703 Sfmt 4703 E:\FR\FM\16MYN1.SGM 16MYN1](https://thefederalregister.org/doc/81_FR_30437/page/1.svg)
![30344 Federal Register / Vol. 81, No. 94 / Monday, May 16, 2016 / Notices
SUMMARY: Siegfried USA, LLC applied to DEPARTMENT OF JUSTICE In reference to drug codes 7360
be registered as an importer of certain (marihuana), and 7370 (THC), the
basic classes of controlled substances. Drug Enforcement Administration company plans to bulk manufacture
The Drug Enforcement Administration these drugs as synthetics. No other
[Docket No. DEA–392] activity for these drug codes are
(DEA) grants Siegfried USA, LLC
registration as an importer of those authorized for this registration.
Manufacturer of Controlled
controlled substances. Substances Registration: AMRI Dated: April 28, 2016.
SUPPLEMENTARY INFORMATION: By notice Rensselaer, Inc. Louis J. Milione,
dated January 11, 2016, and published Deputy Assistant Administrator.
ACTION: Notice of registration. [FR Doc. 2016–11392 Filed 5–13–16; 8:45 am]
in the Federal Register on January 19,
2016, 81 FR 2910, Siegfried USA, LLC, SUMMARY: AMRI Rensselaer, Inc. applied BILLING CODE 4410–09–P
33 Industrial Park Road, Pennsville, to be registered as a manufacturer of
New Jersey 08070 applied to be certain basic classes of controlled
DEPARTMENT OF JUSTICE
registered as an importer of certain basic substances. The Drug Enforcement
classes of controlled substances. Administration (DEA) grants AMRI Drug Enforcement Administration
Comments and requests for hearings on Rensselaer, Inc. registration as a
applications to import narcotic raw manufacturer of those controlled
[Docket No. DEA–392]
material are not appropriate. 72 FR substances.
3417, (January 25, 2007). SUPPLEMENTARY INFORMATION: By notice Manufacturer of Controlled
The DEA has considered the factors in dated November 30, 2015, and Substances Registration: Johnson
21 U.S.C. 823, 952(a) and 958(a) and published in the Federal Register on Matthey, Inc.
determined that the registration of December 8, 2015, 80 FR 76312, AMRI
Siegfried USA, LLC to import the basic Rensselaer, Inc., 33 Riverside Avenue, ACTION: Notice of registration.
classes of controlled substances is Rensselaer, New York 12144 applied to
be registered as a manufacturer of SUMMARY: Johnson Matthey, Inc. applied
consistent with the public interest and
certain basic classes of controlled to be registered as a manufacturer of
with United States obligations under
substances. No comments or objections certain basic classes of controlled
international treaties, conventions, or
were submitted for this notice. substances. The Drug Enforcement
protocols in effect on May 1, 1971. The
DEA investigated the company’s The DEA has considered the factors in Administration (DEA) grants Johnson
21 U.S.C. 823(a) and determined that Matthey, Inc. registration as a
maintenance of effective controls
the registration of AMRI Rensselaer, Inc. manufacturer of those controlled
against diversion by inspecting and substances.
to manufacture the basic classes of
testing the company’s physical security
controlled substances is consistent with SUPPLEMENTARY INFORMATION: By notice
systems, verifying the company’s the public interest and with United
compliance with state and local laws, dated December 9, 2015, and published
States obligations under international in the Federal Register on December 17,
and reviewing the company’s treaties, conventions, or protocols in
background and history. 2015, 80 FR 78765, Johnson Matthey,
effect on May 1, 1971. The DEA Inc., Custom Pharmaceuticals
Therefore, pursuant to 21 U.S.C. investigated the company’s maintenance Department, 2003 Nolte Drive, West
952(a) and 958(a), and in accordance of effective controls against diversion by Deptford, New Jersey 08066–1742
with 21 CFR 1301.34, the above-named inspecting and testing the company’s applied to be registered as a
company is granted registration as an physical security systems, verifying the manufacturer of certain basic classes of
importer of the following basic classes company’s compliance with state and controlled substances. No comments or
of controlled substances: local laws, and reviewing the company’s objections were submitted for this
background and history. notice.
Controlled substance Schedule Therefore, pursuant to 21 U.S.C.
The DEA has considered the factors in
823(a), and in accordance with 21 CFR
21 U.S.C. 823(a) and determined that
Opium, raw (9600) ....................... II 1301.33, the above-named company is
the registration of Johnson Matthey, Inc.
Poppy Straw Concentrate (9670) II granted registration as a bulk
to manufacture the basic classes of
manufacturer of the following basic
controlled substances is consistent with
The company plans to import the classes of controlled substances:
the public interest and with United
listed controlled substances to
Controlled substance Schedule States obligations under international
manufacture bulk active pharmaceutical treaties, conventions, or protocols in
ingredients (API) for distribution to its Marihuana (7360) ......................... I effect on May 1, 1971. The DEA
customer. Tetrahydrocannabinols (7370) ..... I investigated the company’s maintenance
Dated: April 28, 2016. Amphetamine (1100) .................... II of effective controls against diversion by
Lisdexamfetamine (1205) ............. II inspecting and testing the company’s
Louis J. Milione, Methylphenidate (1724) ................ II physical security systems, verifying the
Deputy Assistant Administrator. Pentobarbital (2270) ..................... II
company’s compliance with state and
asabaliauskas on DSK3SPTVN1PROD with NOTICES
[FR Doc. 2016–11414 Filed 5–13–16; 8:45 am] 4-Anilino-N-phenethyl-4-piperidine II
(ANPP) (8333). local laws, and reviewing the company’s
BILLING CODE 4410–09–P
Meperidine (9230) ........................ II background and history.
Fentanyl (9801) ............................ II Therefore, pursuant to 21 U.S.C.
823(a), and in accordance with 21 CFR
The company plans to manufacture 1301.33, the above-named company is
bulk controlled substances for use in granted registration as a bulk
product development and for manufacturer of the following basic
distribution to its customers. classes of controlled substances:
VerDate Sep<11>2014 18:48 May 13, 2016 Jkt 238001 PO 00000 Frm 00108 Fmt 4703 Sfmt 4703 E:\FR\FM\16MYN1.SGM 16MYN1](https://thefederalregister.org/doc/81_FR_30437/page/2.svg)
Document Created: 2016-05-14 01:17:06
Document Modified: 2016-05-14 01:17:06
| 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 | 81 FR 30343 |
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