81 FR 34372 - Importer of Controlled Substances Application: Wildlife Laboratories, Inc.
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 81, Issue 104 (May 31, 2016)
Drug Enforcement Administration
Federal Register Volume 81, Issue 104 (May 31, 2016)
| Page Range | 34372-34372 | |
| FR Document | 2016-12751 |
[Federal Register Volume 81, Number 104 (Tuesday, May 31, 2016)] [Notices] [Page 34372] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-12751] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Importer of Controlled Substances Application: Wildlife Laboratories, Inc. AGENCY: Drug Enforcement Administration, DOJ. 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 in accordance with 21 CFR 1301.34(a) on or before June 30, 2016. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before June 30, 2016. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Attn: DEA Federal Register Representative/ODW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The Attorney General has delegated her 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 Deputy Assistant Administrator of the DEA Office of Diversion Control (``Deputy 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 February 19, 2016, Wildlife Laboratories, Inc., 1230 W. Ash Street, Suite D, Windsor, Colorado 80550-8055 applied to be registered as an importer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Schedule ------------------------------------------------------------------------ Etorphine (except HCl) (9056)................ I Etorphine HCl (9059)......................... II ------------------------------------------------------------------------ The company plans to import the listed controlled substances for sale to its customer. Dated: May 19, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016-12751 Filed 5-27-16; 8:45 am] BILLING CODE 4410-09-P
![34372 Federal Register / Vol. 81, No. 104 / Tuesday, May 31, 2016 / Notices
The Attorney General has delegated DEPARTMENT OF JUSTICE of the following basic classes of
her authority under the Controlled controlled substances:
Substances Act to the Administrator of Drug Enforcement Administration
the Drug Enforcement Administration Sched-
Controlled substance ule
(DEA), 28 CFR 0.100(b). Authority to [Docket No. DEA–392]
exercise all necessary functions with Etorphine (except HCl) (9056) .......... I
respect to the promulgation and Importer of Controlled Substances Etorphine HCl (9059) ........................ II
implementation of 21 CFR part 1301, Application: Wildlife Laboratories, Inc.
incident to the registration of AGENCY: Drug Enforcement The company plans to import the
manufacturers, distributors, dispensers, Administration, DOJ. listed controlled substances for sale to
importers, and exporters of controlled its customer.
ACTION: Notice of application.
substances (other than final orders in Dated: May 19, 2016.
connection with suspension, denial, or DATES: Registered bulk manufacturers of Louis J. Milione,
revocation of registration) has been the affected basic classes, and Deputy Assistant Administrator.
redelegated to the Deputy Assistant applicants therefore, may file written [FR Doc. 2016–12751 Filed 5–27–16; 8:45 am]
Administrator of the DEA Office of comments on or objections to the BILLING CODE 4410–09–P
Diversion Control (‘‘Deputy Assistant issuance of the proposed registration in
Administrator’’) pursuant to section 7 of accordance with 21 CFR 1301.34(a) on
28 CFR part 0, appendix to subpart R. or before June 30, 2016. Such persons DEPARTMENT OF LABOR
In accordance with 21 CFR may also file a written request for a
hearing on the application pursuant to Office of the Secretary
1301.33(a), this is notice that on March
21 CFR 1301.43 on or before June 30,
26, 2016, Rhodes Technologies, 498
2016. Agency Information Collection
Washington Street, Coventry, Rhode Activities; Submission for OMB
Island 02816 applied to be registered as ADDRESSES: Written comments should
be sent to: Drug Enforcement Review; Comment Request; Trade
a bulk manufacturer the following basic Adjustment Assistance Program
classes of controlled substances: Administration, Attention: DEA Federal
Register Representative/ODW, 8701 Reserve Funding Request
Controlled substance Schedule Morrissette Drive, Springfield, Virginia ACTION: Notice.
22152. All requests for hearing must be
Tetrahydrocannabinols (7370) ..... I sent to: Drug Enforcement SUMMARY: The Department of Labor
Dihydromorphine (9145) ............... I Administration, Attn: Administrator, (DOL) is submitting the Employment
Methylphenidate (1724) ................ II 8701 Morrissette Drive, Springfield, and Training Administration (ETA)
Codeine (9050) ............................. II Virginia 22152. All requests for hearing sponsored information collection
Dihydrocodeine (9120) ................. II should also be sent to: (1) Drug request (ICR) titled, ‘‘Trade Adjustment
Oxycodone (9143) ........................ II Enforcement Administration, Attn: Assistance Program Reserve Funding
Hydromorphone (9150) ................ II Hearing Clerk/LJ, 8701 Morrissette Request,’’ to the Office of Management
Hydrocodone (9193) ..................... II Drive, Springfield, Virginia 22152; and and Budget (OMB) for review and
Levorphanol (9220) ...................... II (2) Drug Enforcement Administration, approval for continued use, without
Morphine (9300) ........................... II Attn: DEA Federal Register change, in accordance with the
Oripavine (9330) ........................... II Representative/ODW, 8701 Morrissette Paperwork Reduction Act of 1995
Oxymorphone (9652) ................... II Drive, Springfield, Virginia 22152. (PRA), 44 U.S.C. 3501 et seq. Public
Noroxymorphone (9668) .............. II SUPPLEMENTARY INFORMATION: The comments on the ICR are invited.
Tapentadol (9780) ........................ II Attorney General has delegated her DATES: The OMB will consider all
Fentanyl (9801) ............................ II written comments that agency receives
authority under the Controlled
Substances Act to the Administrator of on or before June 30, 2016.
The company plans to manufacture the Drug Enforcement Administration ADDRESSES: A copy of this ICR with
the listed controlled substances in bulk (DEA), 28 CFR 0.100(b). Authority to applicable supporting documentation;
for conversion and sale to dosage form exercise all necessary functions with including a description of the likely
manufacturers. respect to the promulgation and respondents, proposed frequency of
In reference to drug code 7370 the implementation of 21 CFR part 1301, response, and estimated total burden
company plans to bulk manufacture a incident to the registration of may be obtained free of charge from the
synthetic tetrahydrocannabinol. No manufacturers, distributors, dispensers, RegInfo.gov Web site at http://
other activity for this drug code is importers, and exporters of controlled www.reginfo.gov/public/do/
substances (other than final orders in PRAViewICR?ref_nbr=201605-1205-009
authorized for this registration.
connection with suspension, denial, or (this link will only become active on the
Dated: May 19, 2016. revocation of registration) has been day following publication of this notice)
Louis J. Milione, redelegated to the Deputy Assistant or by contacting Michel Smyth by
Deputy Assistant Administrator. Administrator of the DEA Office of telephone at 202–693–4129, TTY 202–
[FR Doc. 2016–12752 Filed 5–27–16; 8:45 am] Diversion Control (‘‘Deputy Assistant 693–8064, (these are not toll-free
Administrator’’) pursuant to section 7 of numbers) or by email at DOL_PRA_
sradovich on DSK3TPTVN1PROD with NOTICES
BILLING CODE 4410–09–P
28 CFR part 0, appendix to subpart R. PUBLIC@dol.gov.
In accordance with 21 CFR Submit comments about this request
1301.34(a), this is notice that on by mail or courier to the Office of
February 19, 2016, Wildlife Information and Regulatory Affairs,
Laboratories, Inc., 1230 W. Ash Street, Attn: OMB Desk Officer for DOL–ETA,
Suite D, Windsor, Colorado 80550–8055 Office of Management and Budget,
applied to be registered as an importer Room 10235, 725 17th Street NW.,
VerDate Sep<11>2014 20:07 May 27, 2016 Jkt 238001 PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 E:\FR\FM\31MYN1.SGM 31MYN1](https://thefederalregister.org/doc/81_FR_34476/page/1.svg)
Document Created: 2016-05-28 03:57:39
Document Modified: 2016-05-28 03:57:39
| 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 in accordance with 21 CFR 1301.34(a) on or before June 30, 2016. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before June 30, 2016. | |
| FR Citation | 81 FR 34372 |
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