81 FR 63222 - Importer of Controlled Substances Registration
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 81, Issue 178 (September 14, 2016)
Drug Enforcement Administration
Federal Register Volume 81, Issue 178 (September 14, 2016)
| Page Range | 63222-63222 | |
| FR Document | 2016-22083 |
[Federal Register Volume 81, Number 178 (Wednesday, September 14, 2016)] [Notices] [Page 63222] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-22083] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Importer of Controlled Substances Registration ACTION: Notice of registration. ----------------------------------------------------------------------- SUMMARY: 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. SUPPLEMENTARY INFORMATION: The companies listed below applied to be registered as importers of various basic 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. ------------------------------------------------------------------------ Company FR docket Published ------------------------------------------------------------------------ Wildlife Laboratories, Inc.... 81 FR 34372.... May 31, 2016. Janssen Pharmaceutical, Inc... 81 FR 45306.... July 13, 2016. Noramco, Inc.................. 81 FR 45307.... July 13, 2016. ------------------------------------------------------------------------ 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 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 registration as importers for schedule I or II controlled substances to the above listed persons. Dated: September 7, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016-22083 Filed 9-13-16; 8:45 am] BILLING CODE 4410-09-P
![63222 Federal Register / Vol. 81, No. 178 / Wednesday, September 14, 2016 / Notices
DEPARTMENT OF JUSTICE applications to import narcotic raw The company plans to import the
material are not appropriate. 72 FR listed controlled substances for internal
Drug Enforcement Administration 3417, (January 25, 2007). use, and to manufacture bulk
[Docket No. DEA–392] SUPPLEMENTARY INFORMATION: The intermediates for sale to its customers.
Attorney General has delegated her Dated: September 7, 2016.
Importer of Controlled Substances authority under the Controlled
Louis J. Milione,
Application: Cambrex Charles City Substances Act to the Administrator of
the Drug Enforcement Administration Deputy Assistant Administrator.
ACTION: Notice of application. (DEA), 28 CFR 0.100(b). Authority to [FR Doc. 2016–22077 Filed 9–13–16; 8:45 am]
exercise all necessary functions with BILLING CODE 4410–09–P
DATES: Registered bulk manufacturers of
respect to the promulgation and
the affected basic classes, and
implementation of 21 CFR part 1301,
applicants therefore, may file written DEPARTMENT OF JUSTICE
incident to the registration of
comments on or objections to the
manufacturers, distributors, dispensers,
issuance of the proposed registration in Drug Enforcement Administration
importers, and exporters of controlled
accordance with 21 CFR 1301.34(a) on
substances (other than final orders in
or before October 14, 2016. Such
connection with suspension, denial, or [Docket No. DEA–392]
persons may also file a written request
revocation of registration) has been
for a hearing on the application
redelegated to the Deputy Assistant Importer of Controlled Substances
pursuant to 21 CFR 1301.43 on or before
October 14, 2016. Administrator of the DEA Office of Registration
Diversion Control (‘‘Deputy Assistant
ADDRESSES: Written comments should
Administrator’’) pursuant to section 7 of ACTION: Notice of registration.
be sent to: Drug Enforcement
28 CFR part 0, appendix to subpart R.
Administration, Attention: DEA Federal In accordance with 21 CFR
Register Representative/ODW, 8701 SUMMARY: Registrants listed below have
1301.34(a), this is notice that on May 5, applied for and been granted
Morrissette Drive, Springfield, Virginia 2016, Cambrex Charles City, 1205 11th
22152. All requests for hearing must be registration by the Drug Enforcement
Street, Charles City, Iowa 50616–3466 Administration (DEA) as importers of
sent to: Drug Enforcement applied to be registered as an importer
Administration, Attn: Administrator, various classes of schedule I or II
of the following basic classes of
8701 Morrissette Drive, Springfield, controlled substances.
controlled substances:
Virginia 22152. All requests for hearing
SUPPLEMENTARY INFORMATION: The
should also be sent to: (1) Drug Controlled substance Schedule
Enforcement Administration, Attn: companies listed below applied to be
Hearing Clerk/LJ, 8701 Morrissette registered as importers of various basic
4-Anilino-N-phenethyl-4-piperidine II
Drive, Springfield, Virginia 22152; and (ANPP) (8333). classes of controlled substances.
(2) Drug Enforcement Administration, Phenylacetone (8501) .................. II Information on previously published
Attn: DEA Federal Register Coca Leaves (9040) ..................... II notices is listed in the table below. No
Representative/ODW, 8701 Morrissette Opium, raw (9600) ....................... II comments or objections were submitted
Alfentanil (9737) ........................... II and no requests for hearing were
Drive, Springfield, Virginia 22152. Poppy Straw Concentrate (9670) II
Comments and request for hearing on submitted for these notices.
Company FR docket Published
Wildlife Laboratories, Inc ......................................................................................................... 81 FR 34372 .......................... May 31, 2016.
Janssen Pharmaceutical, Inc ................................................................................................... 81 FR 45306 .......................... July 13, 2016.
Noramco, Inc ........................................................................................................................... 81 FR 45307 .......................... July 13, 2016.
The DEA has considered the factors in granted registration as importers for DATES: Registered bulk manufacturers of
21 U.S.C. 823, 952(a) and 958(a) and schedule I or II controlled substances to the affected basic classes, and
determined that the registration of the the above listed persons. applicants therefore, may file written
listed registrants to import the Dated: September 7, 2016. comments on or objections to the
applicable basic classes of schedule I or Louis J. Milione,
issuance of the proposed registration in
II controlled substances is consistent accordance with 21 CFR 1301.33(a) on
Deputy Assistant Administrator.
with the public interest and with United or before November 14, 2016.
[FR Doc. 2016–22083 Filed 9–13–16; 8:45 am]
States obligations under international ADDRESSES: Written comments should
treaties, conventions, or protocols in BILLING CODE 4410–09–P
be sent to: Drug Enforcement
effect on May 1, 1971. The DEA Administration, Attention: DEA Federal
investigated each company’s Register Representative/ODW, 8701
DEPARTMENT OF JUSTICE
maintenance of effective controls Morrissette Drive, Springfield, Virginia
against diversion by inspecting and
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Drug Enforcement Administration 22152.
testing each company’s physical
security systems, verifying each [Docket No. DEA–392] SUPPLEMENTARY INFORMATION: The
company’s compliance with state and Attorney General has delegated her
local laws, and reviewing each Bulk Manufacturer of Controlled authority under the Controlled
company’s background and history. Substances Application: AMPAC Fine Substances Act to the Administrator of
Therefore, pursuant to 21 U.S.C. Chemicals LLC the Drug Enforcement Administration
952(a) and 958(a), and in accordance (DEA), 28 CFR 0.100(b). Authority to
ACTION: Notice of application.
with 21 CFR 1301.34, the DEA has exercise all necessary functions with
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Document Created: 2016-09-14 02:27:19
Document Modified: 2016-09-14 02:27:19
| 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 registration. | |
| FR Citation | 81 FR 63222 |
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