Bulk Manufacturer of Controlled Substances Registration, 2577 [2019-01525]

Download as PDF 2577 Federal Register / Vol. 84, No. 26 / Thursday, February 7, 2019 / Notices Registrants listed below have applied for and been granted registration by-the Drug Enforcement Administration (DEA) as importers of various classes of schedule I or II controlled substances. SUMMARY: DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Registration ACTION: classes of controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted and no requests for hearing were submitted for these notices. The companies listed below applied to be registered as importers of various basic SUPPLEMENTARY INFORMATION: Notice of registration. Company FR docket Noramco Inc ...................................................................................................................................................... Catalent CTS, LLC ............................................................................................................................................ United States Pharmacopeial Convention ........................................................................................................ Fisher Clinical Services, Inc ............................................................................................................................. Cambrex High Point, Inc ................................................................................................................................... Sharp (Bethlehem), LLC ................................................................................................................................... The DEA has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of the listed registrants to import the applicable basic classes of schedule I or II 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 of the 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. 952(a) and 958(a), and in accordance with 21 CFR 1301.34, the DEA has granted a registration as an importer for schedule I or II controlled substances to the above listed companies. Dated: December 21, 2018. John J. Martin, Assistant Administrator. 83 83 83 83 83 83 FR FR FR FR FR FR 53107 54613 54611 54612 54610 54612 The companies listed below applied to be registered as bulk manufacturers of various basic classes of controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted for these notices. BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Bulk Manufacturer of Controlled Substances Registration ACTION: Notice of registration. 83 FR 48334 83 FR 49578 Jkt 247001 2018. 2018. 2018. 2018. 2018. 2018. SUPPLEMENTARY INFORMATION: [FR Doc. 2019–01519 Filed 2–6–19; 8:45 am] AMPAC Fine Chemicals Virginia, LLC .......................................................................................................... AMPAC Fine Chemicals, LLC ....................................................................................................................... 17:23 Feb 06, 2019 19, 30, 30, 30, 30, 30, The registrants listed below has applied for and has been granted registration by the Drug Enforcement Administration (DEA) as bulk manufacturer of various classes of schedule I and II controlled substances. FR Docket VerDate Sep<11>2014 October October October October October October SUMMARY: Company The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of this registrant 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 the company’s maintenance of effective controls against diversion by inspecting and testing their physical security systems, verifying their compliance with state and local laws, and reviewing each of the 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 Published registration as a bulk manufacturer to the above listed companies. Dated: December 21, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2019–01525 Filed 2–6–19; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 2018–43] Kurt L. Pflieger, M.D.; Order Dismissing Order To Show Cause On July 12, 2018, the Assistant Administrator, Diversion Control Division, Drug Enforcement PO 00000 Frm 00091 Fmt 4703 Sfmt 4703 Published September 24, 2018. October 2, 2018. Administration (hereinafter, DEA or Government), issued an Order to Show Cause to Kurt L. Pflieger, M.D. (hereinafter, Respondent), of Rockwall, Texas. Order to Show Cause (hereinafter, OSC), at 1. The OSC proposes the revocation of Respondent’s Certificate of Registration on the ground that he does not have authority to handle controlled substances in the State of Texas, the State in which he is registered with the DEA. Id. After the Administrative Law Judge (hereinafter, ALJ) certified and transmitted the record to me along with his Recommended Decision, the Government submitted a ‘‘Motion to Dismiss Order to Show Cause’’ (hereinafter, Motion). According to the Motion, the Texas Medical Board held E:\FR\FM\07FEN1.SGM 07FEN1

Agencies

[Federal Register Volume 84, Number 26 (Thursday, February 7, 2019)]
[Notices]
[Page 2577]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-01525]


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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: The registrants listed below has applied for and has been 
granted registration by the Drug Enforcement Administration (DEA) as 
bulk manufacturer of various classes of schedule I and II controlled 
substances.

SUPPLEMENTARY INFORMATION: The companies listed below applied to be 
registered as bulk manufacturers of various basic classes of 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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AMPAC Fine Chemicals Virginia, LLC.......  83 FR 48334                    September 24, 2018.
AMPAC Fine Chemicals, LLC................  83 FR 49578                    October 2, 2018.
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    The DEA has considered the factors in 21 U.S.C. 823(a) and 
determined that the registration of this registrant 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 the company's maintenance of effective 
controls against diversion by inspecting and testing their physical 
security systems, verifying their compliance with state and local laws, 
and reviewing each of the 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: December 21, 2018.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-01525 Filed 2-6-19; 8:45 am]
 BILLING CODE 4410-09-P
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