82 FR 61795 - Bulk Manufacturer of Controlled Substances Application: AMPAC Fine Chemicals LLC
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 82, Issue 249 (December 29, 2017)
Drug Enforcement Administration
Federal Register Volume 82, Issue 249 (December 29, 2017)
| Page Range | 61795-61795 | |
| FR Document | 2017-28178 |
[Federal Register Volume 82, Number 249 (Friday, December 29, 2017)] [Notices] [Page 61795] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-28178] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Application: AMPAC Fine Chemicals LLC ACTION: Notice of application. ----------------------------------------------------------------------- DATES: 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 February 27, 2018. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: 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 October 28, 2016, AMPAC Fine Chemicals Virginia, LLC, 2820 North Normandy Drive, Petersburg, Virginia 23805-2380 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Drug code Schedule ------------------------------------------------------------------------ Methylphenidate...................... 1724 II Levomethorphan....................... 9210 II Levorphanol.......................... 9220 II ------------------------------------------------------------------------ The company plans to manufacture the listed controlled substances in bulk for distribution to its customers. Dated: December 15, 2017. Demetra Ashley, Acting Assistant Administrator. [FR Doc. 2017-28178 Filed 12-28-17; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 82, No. 249 / Friday, December 29, 2017 / Notices 61795
DEPARTMENT OF JUSTICE comments on or objections to the of application that inadvertently
issuance of the proposed registration on misstated what the firm plans to do with
Antitrust Division or before February 27, 2018. imported tapentadol.
ADDRESSES: Written comments should Correction
Notice Pursuant to the National be sent to: Drug Enforcement
Cooperative Research and Production Administration, Attention: DEA Federal In the Federal Register of December 1,
Act of 1993—Network Centric Register Representative/DRW, 8701 2017, in FR Doc. 2017–25921 (82 FR
Operations Industry Consortium, Inc. Morrissette Drive, Springfield, Virginia 230), on page 230, in the second
22152. column, the last paragraph, correct the
Notice is hereby given that, on
first sentence to read: The company
December 5, 2017, pursuant to Section SUPPLEMENTARY INFORMATION: The plans to import bulk tapentadol (9780)
6(a) of the National Cooperative Attorney General has delegated his to manufacture dosage form tapentadol
Research and Production Act of 1993, authority under the Controlled (9780) for distribution to its customers.
15 U.S.C. 4301 et seq. (‘‘the Act’’), Substances Act to the Administrator of
Network Centric Operations Industry the Drug Enforcement Administration Demetra Ashley,
Consortium, Inc. (‘‘NCOIC’’) has filed (DEA), 28 CFR 0.100(b). Authority to Acting Assistant Administrator.
written notifications simultaneously exercise all necessary functions with [FR Doc. 2017–28176 Filed 12–28–17; 8:45 am]
with the Attorney General and the respect to the promulgation and BILLING CODE 4410–09–P
Federal Trade Commission disclosing implementation of 21 CFR part 1301,
changes in its membership. The incident to the registration of
notifications were filed for the purpose manufacturers, distributors, dispensers, DEPARTMENT OF JUSTICE
of extending the Act’s provisions importers, and exporters of controlled
limiting the recovery of antitrust substances (other than final orders in Drug Enforcement Administration
plaintiffs to actual damages under connection with suspension, denial, or [Docket No. DEA–392]
specified circumstances. Specifically, revocation of registration) has been
Marc Fiammante (individual member), redelegated to the Assistant Bulk Manufacturer of Controlled
Alpes Maritimes, FRANCE, has been Administrator of the DEA Diversion Substances Application: Cambrex
added as a party to this venture. Control Division (‘‘Assistant High Point, Inc.
No other changes have been made in Administrator’’) pursuant to section 7 of
either the membership or planned 28 CFR part 0, appendix to subpart R. ACTION: Notice of application.
activity of the group research project. In accordance with 21 CFR
Membership in this group research DATES: Registered bulk manufacturers of
1301.33(a), this is notice that on October
project remains open, and NCOIC the affected basic classes, and
28, 2016, AMPAC Fine Chemicals
intends to file additional written applicants therefore, may file written
Virginia, LLC, 2820 North Normandy
notifications disclosing all changes in comments on or objections to the
Drive, Petersburg, Virginia 23805–2380
membership. issuance of the proposed registration on
applied to be registered as a bulk
On November 19, 2004, NCOIC filed or before February 27, 2018.
manufacturer of the following basic
its original notification pursuant to ADDRESSES: Written comments should
classes of controlled substances:
Section 6(a) of the Act. The Department be sent to: Drug Enforcement
of Justice published a notice in the Controlled Administration, Attention: DEA Federal
Drug code Schedule Register Representative/DRW, 8701
Federal Register pursuant to Section substance
6(b) of the Act on February 2, 2005 (70 Morrissette Drive, Springfield, Virginia
FR 5486). Methylphenidate ... 1724 II 22152.
The last notification was filed with Levomethorphan ... 9210 II
Levorphanol .......... 9220 II SUPPLEMENTARY INFORMATION: The
the Department on July 11, 2017. A Attorney General has delegated his
notice was published in the Federal The company plans to manufacture authority under the Controlled
Register pursuant to Section 6(b) of the the listed controlled substances in bulk Substances Act to the Administrator of
Act on August 15, 2017 (82 FR 38711). for distribution to its customers. the Drug Enforcement Administration
Patricia A. Brink, Dated: December 15, 2017. (DEA), 28 CFR 0.100(b). Authority to
Director of Civil Enforcement, Antitrust exercise all necessary functions with
Demetra Ashley,
Division. respect to the promulgation and
Acting Assistant Administrator.
[FR Doc. 2017–28129 Filed 12–28–17; 8:45 am] implementation of 21 CFR part 1301,
[FR Doc. 2017–28178 Filed 12–28–17; 8:45 am]
BILLING CODE P
incident to the registration of
BILLING CODE 4410–09–P manufacturers, distributors, dispensers,
importers, and exporters of controlled
DEPARTMENT OF JUSTICE substances (other than final orders in
DEPARTMENT OF JUSTICE
connection with suspension, denial, or
Drug Enforcement Administration Drug Enforcement Administration revocation of registration) has been
redelegated to the Assistant
[Docket No. DEA–392] [Docket No. DEA–392] Administrator of the DEA Diversion
Bulk Manufacturer of Controlled Control Division (‘‘Assistant
Importer of Controlled Substances
Substances Application: AMPAC Fine Administrator’’) pursuant to section 7 of
ethrower on DSK3G9T082PROD with NOTICES
Application: ABBVIE LTD; Correction
Chemicals LLC 28 CFR part 0, appendix to subpart R.
ACTION: Notice; correction. In accordance with 21 CFR
ACTION: Notice of application. 1301.33(a), this is notice that on
SUMMARY: The Drug Enforcement November 22, 2016, Cambrex High
DATES: Registered bulk manufacturers of Administration (DEA) published a Point, Inc., 4180 Mendenhall Oaks
the affected basic classes, and document in the Federal Register of Parkway, High Point, North Carolina
applicants therefore, may file written December 1, 2017, concerning a notice 27265 applied to be registered as a bulk
VerDate Sep<11>2014 20:09 Dec 28, 2017 Jkt 244001 PO 00000 Frm 00068 Fmt 4703 Sfmt 4703 E:\FR\FM\29DEN1.SGM 29DEN1](https://thefederalregister.org/doc/82_FR_62044/page/1.svg)
Document Created: 2018-01-03 13:16:49
Document Modified: 2018-01-03 13:16:49
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice of application. | |
| Dates | 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 February 27, 2018. | |
| FR Citation | 82 FR 61795 |
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