Manufacturer of Controlled Substances Registration: AMRI Rensselaer, Inc., 30344 [2016-11392]

Download as PDF 30344 Federal Register / Vol. 81, No. 94 / Monday, May 16, 2016 / Notices 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. SUMMARY: 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: SUPPLEMENTARY INFORMATION: Controlled substance Schedule Opium, raw (9600) ....................... Poppy Straw Concentrate (9670) II II asabaliauskas on DSK3SPTVN1PROD with NOTICES 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 VerDate Sep<11>2014 18:48 May 13, 2016 Jkt 238001 DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Manufacturer of Controlled Substances Registration: AMRI Rensselaer, Inc. ACTION: Notice of registration. In reference to drug codes 7360 (marihuana), and 7370 (THC), the company plans to bulk manufacture these drugs as synthetics. No other activity for these drug codes are authorized for this registration. Dated: April 28, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016–11392 Filed 5–13–16; 8:45 am] AMRI Rensselaer, Inc. applied BILLING CODE 4410–09–P to be registered as a manufacturer of certain basic classes of controlled DEPARTMENT OF JUSTICE substances. The Drug Enforcement Administration (DEA) grants AMRI Drug Enforcement Administration Rensselaer, Inc. registration as a manufacturer of those controlled [Docket No. DEA–392] substances. Manufacturer of Controlled SUPPLEMENTARY INFORMATION: By notice Substances Registration: Johnson dated November 30, 2015, and Matthey, Inc. published in the Federal Register on December 8, 2015, 80 FR 76312, AMRI ACTION: Notice of registration. Rensselaer, Inc., 33 Riverside Avenue, Rensselaer, New York 12144 applied to SUMMARY: Johnson Matthey, Inc. applied be registered as a manufacturer of to be registered as a manufacturer of certain basic classes of controlled certain basic classes of controlled substances. No comments or objections substances. The Drug Enforcement were submitted for this notice. The DEA has considered the factors in Administration (DEA) grants Johnson Matthey, Inc. registration as a 21 U.S.C. 823(a) and determined that the registration of AMRI Rensselaer, Inc. manufacturer of those controlled substances. to manufacture the basic classes of controlled substances is consistent with SUPPLEMENTARY INFORMATION: By notice the public interest and with United dated December 9, 2015, and published States obligations under international in the Federal Register on December 17, treaties, conventions, or protocols in 2015, 80 FR 78765, Johnson Matthey, effect on May 1, 1971. The DEA Inc., Custom Pharmaceuticals investigated the company’s maintenance Department, 2003 Nolte Drive, West of effective controls against diversion by Deptford, New Jersey 08066–1742 inspecting and testing the company’s applied to be registered as a physical security systems, verifying the manufacturer of certain basic classes of company’s compliance with state and controlled substances. No comments or local laws, and reviewing the company’s objections were submitted for this background and history. notice. 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 1301.33, the above-named company is the registration of Johnson Matthey, Inc. granted registration as a bulk to manufacture the basic classes of manufacturer of the following basic controlled substances is consistent with classes of controlled substances: the public interest and with United Controlled substance Schedule States obligations under international treaties, conventions, or protocols in effect on May 1, 1971. The DEA Marihuana (7360) ......................... I Tetrahydrocannabinols (7370) ..... I investigated the company’s maintenance Amphetamine (1100) .................... II of effective controls against diversion by Lisdexamfetamine (1205) ............. II inspecting and testing the company’s Methylphenidate (1724) ................ II physical security systems, verifying the Pentobarbital (2270) ..................... II company’s compliance with state and 4-Anilino-N-phenethyl-4-piperidine II local laws, and reviewing the company’s (ANPP) (8333). background and history. Meperidine (9230) ........................ II Therefore, pursuant to 21 U.S.C. Fentanyl (9801) ............................ II 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: SUMMARY: PO 00000 Frm 00108 Fmt 4703 Sfmt 4703 E:\FR\FM\16MYN1.SGM 16MYN1

Agencies

[Federal Register Volume 81, Number 94 (Monday, May 16, 2016)]
[Notices]
[Page 30344]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-11392]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Manufacturer of Controlled Substances Registration: AMRI 
Rensselaer, Inc.

ACTION: Notice of registration.

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SUMMARY: AMRI Rensselaer, Inc. applied to be registered as a 
manufacturer of certain basic classes of controlled substances. The 
Drug Enforcement Administration (DEA) grants AMRI Rensselaer, Inc. 
registration as a manufacturer of those controlled substances.

SUPPLEMENTARY INFORMATION: By notice dated November 30, 2015, and 
published in the Federal Register on December 8, 2015, 80 FR 76312, 
AMRI Rensselaer, Inc., 33 Riverside Avenue, Rensselaer, New York 12144 
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 AMRI Rensselaer, 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 following basic classes of controlled substances:

------------------------------------------------------------------------
            Controlled substance                       Schedule
------------------------------------------------------------------------
Marihuana (7360)...........................  I
Tetrahydrocannabinols (7370)...............  I
Amphetamine (1100).........................  II
Lisdexamfetamine (1205)....................  II
Methylphenidate (1724).....................  II
Pentobarbital (2270).......................  II
4-Anilino-N-phenethyl-4-piperidine (ANPP)    II
 (8333).
Meperidine (9230)..........................  II
Fentanyl (9801)............................  II
------------------------------------------------------------------------

    The company plans to manufacture bulk controlled substances for use 
in product development and for distribution to its customers.
    In reference to drug codes 7360 (marihuana), and 7370 (THC), the 
company plans to bulk manufacture these drugs as synthetics. No other 
activity for these drug codes are authorized for this registration.

    Dated: April 28, 2016.
Louis J. Milione,
Deputy Assistant Administrator.
[FR Doc. 2016-11392 Filed 5-13-16; 8:45 am]
 BILLING CODE 4410-09-P

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