Bulk Manufacturer of Controlled Substances Registration AMPAC Fine Chemicals Virginia, LLC, 44640 [2019-18325]

Download as PDF 44640 Federal Register / Vol. 84, No. 165 / Monday, August 26, 2019 / Notices applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before October 25, 2019. ADDRESS: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. In accordance with 21 CFR 1301.33(a), this is notice that on June 19, 2019, Cambrex High Point, Inc., 4180 Mendenhall Oaks Parkway, High Point, North Carolina 27265–8017 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: SUPPLEMENTARY INFORMATION: Controlled substance Oxymorphone ................ Noroxymorphone ........... Drug code 9652 9668 Schedule II II The company plans to manufacture the above listed controlled substances in bulk for distribution to its customers. No other activities for these drug codes are authorized for this registration. Dated: August 9, 2019. Neil D. Doherty, Acting Assistant Administrator. 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. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this is notice that on June 5, 2019, Clinical Supplies Management Holdings, Inc., 342 42nd Street South, Fargo, North Dakota 58103 applied to be registered as an importer of the following basic classes of controlled substances: Drug code Controlled substance Marihuana ..................... Tetrahydrocannabinols 7360 7370 Schedule I I The company plans to import listed controlled substances in their finished dosage form for use in clinical trials only. Drug codes 7350 (marihuana extract) and 7360 (marihuana) will be used for the manufacture of cannabidiol only. Dated: August 9, 2019. Neil D. Doherty, Acting Assistant Administrator. Dated: August 9, 2019. Neil D. Doherty, Acting Assistant Administrator. [FR Doc. 2019–18325 Filed 8–23–19; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] [FR Doc. 2019–18320 Filed 8–23–19; 8:45 am] BILLING CODE 4410–09–P [FR Doc. 2019–18324 Filed 8–23–19; 8:45 am] manufacture the applicable various 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 DEA has granted a registration as a bulk manufacturer to the above listed company. BILLING CODE 4410–09–P Bulk Manufacturer of Controlled Substances Application: AMRI Renesselaer, Inc. ACTION: DEPARTMENT OF JUSTICE DEPARTMENT OF JUSTICE Drug Enforcement Administration Drug Enforcement Administration [Docket No. DEA–392] [Docket No. DEA–392] Bulk Manufacturer of Controlled Substances Registration AMPAC Fine Chemicals Virginia, LLC Importer of Controlled Substances Application: Clinical Supplies Management Holdings, Inc. ACTION: VerDate Sep<11>2014 16:09 Aug 23, 2019 Jkt 247001 Notice of registration. The registrant listed below have applied for and been granted a registration by the Drug Enforcement Administration (DEA) as a bulk manufacturer of various basic classes of schedule II controlled substances. SUPPLEMENTARY INFORMATION: The company listed below applied to be registered as a bulk manufacturer of various basic classes of scheduled II controlled substances. Information on a previously published notice is listed below. No comments or objections were submitted for this notice. SUMMARY: Registered bulk importers 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 September 25, 2019. Such persons may also file a written request for a hearing on the application on or before September 25, 2019. ADDRESSES: 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 DATES: khammond on DSKBBV9HB2PROD with NOTICES ACTION: Notice of application. Company FR docket Published AMPAC Fine Chemicals Virginia, LLC. 84 FR 21810 May 15, 2019. The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of this registrant to PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 Notice of application. 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 October 25, 2019. ADDRESS: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on March 15, 2019, AMRI Rensselaer, Inc., 33 Riverside Avenue, Rennselaer, New York 12144–2951 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: DATES: Controlled substance Marihuana ...................... Tetrahydrocannabinols .. Amphetamine ................ Lisdexamfetamine ......... Pentobarbital ................. 4-Anilino-N-phenethyl-4piperidine (ANPP). Codeine ......................... E:\FR\FM\26AUN1.SGM 26AUN1 Drug code Schedule 7360 7370 1100 1205 2270 8333 I I II II II II 9050 II

Agencies

[Federal Register Volume 84, Number 165 (Monday, August 26, 2019)]
[Notices]
[Page 44640]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-18325]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Registration AMPAC 
Fine Chemicals Virginia, LLC

ACTION: Notice of registration.

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SUMMARY: The registrant listed below have applied for and been granted 
a registration by the Drug Enforcement Administration (DEA) as a bulk 
manufacturer of various basic classes of schedule II controlled 
substances.

SUPPLEMENTARY INFORMATION: The company listed below applied to be 
registered as a bulk manufacturer of various basic classes of scheduled 
II controlled substances. Information on a previously published notice 
is listed below. No comments or objections were submitted for this 
notice.

------------------------------------------------------------------------
             Company                   FR docket           Published
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AMPAC Fine Chemicals Virginia,     84 FR 21810......  May 15, 2019.
 LLC.
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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 various 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 DEA has granted a registration as a bulk manufacturer 
to the above listed company.

    Dated: August 9, 2019.
Neil D. Doherty,
Acting Assistant Administrator.
[FR Doc. 2019-18325 Filed 8-23-19; 8:45 am]
BILLING CODE 4410-09-P
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