Bulk Manufacturer of Controlled Substances Registration, 21810 [2019-10014]

Download as PDF 21810 Federal Register / Vol. 84, No. 94 / Wednesday, May 15, 2019 / Notices hearing on the application on or before June 14, 2019. Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. ADDRESSES: The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Assistant Administrator of the DEA Diversion Control Division (‘‘Assistant Administrator’’) pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.34(a), this is notice that on March 12, 2019, Wildlife Laboratories, Inc., 1230 West Ash, Suite D, Windsor, Colorado 80550–4677 applied to be registered as an importer of the following basic class of controlled substances: SUPPLEMENTARY INFORMATION: Controlled substance Etorphine HCL ............... Thiafentanil .................... Drug code 9059 9729 Schedule II II DEPARTMENT OF JUSTICE Drug Enforcement Administration [FR Doc. 2019–10013 Filed 5–14–19; 8:45 am] [Docket No. DEA–392] jbell on DSK3GLQ082PROD with NOTICES Dated: April 27, 2019. John J. Martin, Assistant Administrator. [FR Doc. 2019–10030 Filed 5–14–19; 8:45 am] BILLING CODE 4410–09–P VerDate Sep<11>2014 22:43 May 14, 2019 BILLING CODE 4410–09–P Bulk Manufacturer of Controlled Substances Application: AMPAC Fine Chemicals Virginia, LLC Notice of application. [Docket No. DEA–392] Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before July 15, 2019. DATES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. ADDRESSES: The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Assistant Administrator of the DEA Diversion Control Division (‘‘Assistant Administrator’’) pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.33(a), this is notice that on March 6, 2019, AMPAC Fine Chemicals Virginia, LLC, 2820 North Normandy Drive, Petersburg, Virginia 23805 applied to be registered as a bulk manufacturer of the following basic class of controlled substances: SUPPLEMENTARY INFORMATION: Methylphenidate ............. Phenylacetone ............... Levomethorphan ............ Levorphanol ................... Morphine ........................ Thebaine ........................ Noroxymorphone ........... Tapentadol ..................... Drug code 1724 8501 9210 9220 9300 9333 9668 9780 Schedule II II II II II II II II The company plans to manufacture the listed controlled substances in bulk for distribution to its customers. Jkt 247001 DEPARTMENT OF JUSTICE Drug Enforcement Administration ACTION: Controlled substance The company plans to import the listed controlled substances for distribution to its customers. Dated: April 27, 2019. John J. Martin, Assistant Administrator. PO 00000 Frm 00063 Fmt 4703 Sfmt 9990 Bulk Manufacturer of Controlled Substances Registration ACTION: Notice of registration. Registrants listed below have applied for and been granted registration by the Drug Enforcement Administration (DEA) as bulk manufacturers of schedule I and II controlled substances. SUMMARY: The companies listed below applied to be registered as bulk manufacturers of schedule I or schedule II controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted for these notices. SUPPLEMENTARY INFORMATION: Company Johnson Matthey Pharmaceutical Materials Inc. IsoSciences, LLC .............. FR docket 84 FR 2579 84 FR 2570 Published February 7, 2019. February 7, 2019. The 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 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 companies. Dated: April 27, 2019. John J. Martin, Assistant Administrator. [FR Doc. 2019–10014 Filed 5–14–19; 8:45 am] BILLING CODE 4410–09–P E:\FR\FM\15MYN1.SGM 15MYN1

Agencies

[Federal Register Volume 84, Number 94 (Wednesday, May 15, 2019)]
[Notices]
[Page 21810]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-10014]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Registration

ACTION: Notice of registration.

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SUMMARY: Registrants listed below have applied for and been granted 
registration by the Drug Enforcement Administration (DEA) as bulk 
manufacturers of schedule I and II controlled substances.

SUPPLEMENTARY INFORMATION: The companies listed below applied to be 
registered as bulk manufacturers of schedule I or schedule II 
controlled substances. Information on previously published notices is 
listed in the table below. No comments or objections were submitted for 
these notices.

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             Company                   FR docket          Published
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Johnson Matthey Pharmaceutical     84 FR 2579......  February 7, 2019.
 Materials Inc.
IsoSciences, LLC.................  84 FR 2570......  February 7, 2019.
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    The 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 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 companies.

    Dated: April 27, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-10014 Filed 5-14-19; 8:45 am]
 BILLING CODE 4410-09-P