Manufacturer of Controlled Substances Registration: Wildlife Laboratories, Inc., 3985 [2015-01294]

Download as PDF Federal Register / Vol. 80, No. 16 / Monday, January 26, 2015 / Notices Controlled substance Schedule Oxycodone (9143) ........................ Hydromorphone (9150) ................ Diphenoxylate (9170) ................... Ecgonine (9180) ........................... Hydrocodone (9193) ..................... Levorphanol (9220) ...................... Meperidine (9230) ........................ Methadone (9250) ........................ Methadone intermediate (9254) ... Dextropropoxyphene, bulk (nondosage forms) (9273). Morphine (9300) ........................... Thebaine (9333) ........................... Opium tincture (9630) .................. Opium, powdered (9639) ............. Oxymorphone (9652) ................... Noroxymorphone (9668) .............. Alfentanil (9737) ........................... Remifentanil (9739) ...................... Sufentanil (9740) .......................... Fentanyl (9801) ............................ II II II II II II II II II II II II II II II II II II II II Controlled substance The company plans to manufacture the listed controlled substances for internal use and for distribution to other companies. Dated: January 9, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015–01304 Filed 1–23–15; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Manufacturer of Controlled Substances Registration: Chattem Chemicals, Inc. ACTION: Notice of registration. Chattem Chemicals, Inc. applied to be registered as a manufacturer of certain basic classes of controlled substances. The DEA grants Chattem Chemicals, Inc. registration as a manufacturer of those controlled substances. SUMMARY: By notice dated August 27, 2014, and published in the Federal Register on September 4, 2014, 79 FR 52764, Chattem Chemicals, Inc., 3801 St. Elmo Avenue, Chattanooga, Tennessee 37409, applied to be registered as a manufacturer of certain basic classes of controlled substances. No comments or objections were submitted to this notice. The Drug Enforcement Administration (DEA) has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Chattem Chemicals, Inc. to manufacture the basic classes of controlled substances is consistent with the public emcdonald on DSK67QTVN1PROD with NOTICES SUPPLEMENTARY INFORMATION: VerDate Sep<11>2014 18:48 Jan 23, 2015 Jkt 235001 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 listed: 3985 DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Manufacturer of Controlled Substances Registration: Wildlife Laboratories, Inc. ACTION: Notice of registration. Schedule Wildlife Laboratories, Inc. applied to be registered as a manufacturer of a basic class of controlled substance. The DEA grants Wildlife Laboratories, Inc. registration as a manufacturer of this controlled substance. I SUPPLEMENTARY INFORMATION: SUMMARY: The company plans to manufacture the listed controlled substances in bulk for distribution and sale to its customers. Regarding (9640) the company plans to manufacture another controlled substance for sale to its customers. By notice dated May 28, 2014, and published in the Federal Register on June 3, 2014, 79 FR 31985, Wildlife Laboratories, Inc., 1230 W. Ash Street, Suite D, Windsor, Colorado 80550, applied to be registered as a manufacturer of a certain basic class of controlled substance. No comments or objections were submitted to this notice. The Drug Enforcement Administration (DEA) has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Wildlife Laboratories, Inc. to manufacture the basic class of controlled substance 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 Carfentanil (9743), a basic class of controlled substance listed in schedule II. The company plans to manufacture the above listed controlled substance for sale to veterinary pharmacies, zoos, and other animal and wildlife applications. Dated: January 9, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. Dated: January 9, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015–01308 Filed 1–23–15; 8:45 am] [FR Doc. 2015–01294 Filed 1–23–15; 8:45 am] BILLING CODE 4410–09–P BILLING CODE P Gamma Hydroxybutyric Acid (2010). 4-Methoxyamphetamine (7411) ... Dihydromorphine (9145) ............... Amphetamine (1100) .................... Methamphetamine (1105) ............ Lisdexamfetamine (1205) ............. Methylphenidate (1724) ................ Pentobarbital (2270) ..................... Codeine (9050) ............................. Dihydrocodeine (9120) ................. Oxycodone (9143) ........................ Hydromorphone (9150) ................ Hydrocodone (9193) ..................... Meperidine (9230) ........................ Meperidine intermediate-A (9232) Meperidine intermediate-B (9233) Meperidine intermediate-C (9234) Methadone (9250) ........................ Methadone intermediate (9254) ... Morphine (9300) ........................... Oripavine (9330) ........................... Thebaine (9333) ........................... Opium tincture (9630) .................. Opium, powdered (9639) ............. Opium, granulated (9640) ............ Oxymorphone (9652) ................... Noroxymorphone (9668) .............. Alfentanil (9737) ........................... Remifentanil (9739) ...................... Sufentanil (9740) .......................... Tapentadol (9780) ........................ Fentanyl (9801) ............................ PO 00000 Frm 00046 Fmt 4703 Sfmt 9990 I I II II II II II II II II II II II II II II II II II II II II II II II II II II II II II E:\FR\FM\26JAN1.SGM 26JAN1

Agencies

[Federal Register Volume 80, Number 16 (Monday, January 26, 2015)]
[Notices]
[Page 3985]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-01294]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Manufacturer of Controlled Substances Registration: Wildlife 
Laboratories, Inc.

ACTION: Notice of registration.

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SUMMARY: Wildlife Laboratories, Inc. applied to be registered as a 
manufacturer of a basic class of controlled substance. The DEA grants 
Wildlife Laboratories, Inc. registration as a manufacturer of this 
controlled substance.

SUPPLEMENTARY INFORMATION: By notice dated May 28, 2014, and published 
in the Federal Register on June 3, 2014, 79 FR 31985, Wildlife 
Laboratories, Inc., 1230 W. Ash Street, Suite D, Windsor, Colorado 
80550, applied to be registered as a manufacturer of a certain basic 
class of controlled substance. No comments or objections were submitted 
to this notice.
    The Drug Enforcement Administration (DEA) has considered the 
factors in 21 U.S.C. 823(a) and determined that the registration of 
Wildlife Laboratories, Inc. to manufacture the basic class of 
controlled substance 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 Carfentanil (9743), a basic class of controlled 
substance listed in schedule II.
    The company plans to manufacture the above listed controlled 
substance for sale to veterinary pharmacies, zoos, and other animal and 
wildlife applications.

    Dated: January 9, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2015-01294 Filed 1-23-15; 8:45 am]
BILLING CODE P

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