Schedules of Controlled Substances: Extension of Temporary Placement of THJ-2201, AB-PINACA and AB-CHMINACA in Schedule I of the Controlled Substances Act, 8590-8592 [2017-01517]
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8590
Federal Register / Vol. 82, No. 17 / Friday, January 27, 2017 / Rules and Regulations
interest pursuant to 5 U.S.C. 553(b)(B).
CBP and Treasury also believe that
affected entities need to be informed as
soon as possible of the extension and its
length in order to plan and adjust their
implementation process accordingly.
Unfunded Mandates Reform Act (Sec.
202, Pub. L. 104–4; 2 U.S.C. 1532)
CBP and Treasury have concluded the
extension of the effective date does not
contain a Federal mandate that may
result in the expenditure by State, local
and Tribal governments, in aggregate, or
by the private sector, of $100 million or
more (adjusted for inflation) in any one
year.
Kevin K. McAleenan,
Acting Commissioner, U.S. Customs and
Border Protection.
Approved: January 25, 2017.
Timothy E. Skud,
Deputy Assistant Secretary of the Treasury.
[FR Doc. 2017–01963 Filed 1–25–17; 4:15 pm]
BILLING CODE 9111–14–P
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
DEPARTMENT OF THE TREASURY
19 CFR Parts 12 and 127
[USCBP–2016–0056; CBP Dec. 16–28]
RIN 1515–AE13
Delay of Effective Date for Toxic
Substance Control Act Chemical
Substance Import Certification
Process Revisions
U.S. Customs and Border
Protection, Department of Homeland
Security; Department of the Treasury.
ACTION: Final rule; delay of effective
date.
AGENCY:
On December 27, 2016, U.S.
Customs and Border Protection (CBP)
published a Final Rule in the Federal
Register announcing amendments to
CBP regulations regarding the
requirement to file a Toxic Substances
Control Act (TSCA) certification when
importing into the customs territory of
the United States chemicals in bulk
form or as part of mixtures and articles
containing a chemical or mixture. That
document amended the regulations to
establish an electronic option for
importers to file the required U.S.
Environmental Protection Agency (EPA)
TSCA certifications, to clarify and add
certain definitions, and to eliminate the
paper-based blanket certification
process. The changes announced in that
jstallworth on DSK7TPTVN1PROD with RULES
SUMMARY:
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13:55 Jan 26, 2017
Jkt 241001
Final Rule were to be effective January
26, 2017. This notice announces that the
effective date of the Final Rule is
delayed for 60 days from January 20,
2017.
This regulation is effective
January 25, 2017. The effective date of
the rule amending 19 CFR parts 12 and
127 published at 81 FR 94980,
December 27, 2016 is delayed until
March 21, 2017.
FOR FURTHER INFORMATION CONTACT: For
questions related to the filing of EPA
forms with CBP, please contact William
Scopa, Partner Government Agencies
Interagency Collaboration Division,
Office of Trade, Customs and Border
Protection, at William.R.Scopa@
cbp.dhs.gov. For EPA policy questions,
please contact Harlan Weir, at
Weir.Harlan@epa.gov.
SUPPLEMENTARY INFORMATION: On
December 27, 2016, U.S. Customs and
Border Protection (CBP) published a
Final Rule in the Federal Register (81
FR 94980) announcing the amendment
of CBP regulations regarding the
requirement to file a Toxic Substances
Control Act (TSCA) certification when
importing into the United States
chemicals in bulk form or as part of
mixtures and articles containing a
chemical or mixture. The document
amended the regulations to permit
importers to file the required U.S.
Environmental Protection Agency (EPA)
TSCA certifications electronically, to
clarify and add certain definitions, and
to eliminate the paper-based blanket
certification process. The final rule was
to become effective on January 26, 2017.
On January 20, 2017, the Chief of Staff
of the White House released a
memorandum to ensure that the
President’s appointees or designees
have the opportunity to review any new
or pending regulations. The
memorandum asks the heads of
executive departments and agencies to
temporarily postpone the effective date
for 60 days from the date of the
memorandum of all regulations that had
been published in the Federal Register,
but had not taken effect. In light of this
memo, CBP has considered whether
entities affected by these final
regulations will need additional time to
implement new systems or internal
procedural changes. To provide
additional time for affected entities to
become familiar with the increased
flexibilities and new processes of the
final regulations, CBP believes that
extending the effective date until March
21, 2017 is appropriate and will furnish
the affected entities with sufficient
additional time.
DATES:
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Executive Order 12866
It has been determined that this final
rule is not a significant regulatory action
as defined in Executive Order 12866.
Therefore, a Regulatory Assessment is
not required.
Regulatory Flexibility Act
Because no notice of proposed
rulemaking is required for this final
rule, the provisions of the Regulatory
Flexibility Act (5 U.S.C. 601 et seq.) do
not apply.
Administrative Procedure Act
CBP and Treasury, for good cause and
the reasons cited above, including the
brief length of the extension of the
effective date, find that notice and
solicitation of comment regarding the
extension of the effective date for the
final regulation are impracticable,
unnecessary, or contrary to the public
interest pursuant to 5 U.S.C. 553(b)(B).
CBP and Treasury also believe that
affected entities need to be informed as
soon as possible of the extension and its
length in order to plan and adjust their
implementation process accordingly.
Unfunded Mandates Reform Act (Sec.
202, Pub. L. 104–4; 2 U.S.C. 1532)
CBP and Treasury have concluded the
extension of the effective date does not
contain a Federal mandate that may
result in the expenditure by State, local
and Tribal governments, in aggregate, or
by the private sector, of $100 million or
more (adjusted for inflation) in any one
year.
Kevin K. McAleenan,
Acting Commissioner, U.S. Customs and
Border Protection.
Approved: January 25, 2017.
Timothy E. Skud,
Deputy Assistant Secretary of the Treasury.
[FR Doc. 2017–01962 Filed 1–25–17; 4:15 pm]
BILLING CODE 9111–14–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA–402]
Schedules of Controlled Substances:
Extension of Temporary Placement of
THJ–2201, AB–PINACA and AB–
CHMINACA in Schedule I of the
Controlled Substances Act
Drug Enforcement
Administration, Department of Justice.
ACTION: Temporary order.
AGENCY:
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Federal Register / Vol. 82, No. 17 / Friday, January 27, 2017 / Rules and Regulations
The Administrator of the Drug
Enforcement Administration is issuing
this temporary order to extend the
temporary schedule I status of three
synthetic cannabinoids pursuant to the
temporary scheduling provisions of the
Controlled Substances Act. The
substances are: [1-(5-Fluoropentyl)-1Hindazol-3-yl](naphthalen-1yl)methanone (THJ–2201); N-1-Amino3-methyl-1-oxo-2-butanyl]-1-pentyl-1Hindazole-3-carboxamide (AB–PINACA);
N-[1-Amino-3-methyl-1-oxo-2-butanyl]1-(cyclohexylmethyl)-1H-indazole-3carboxamide (AB–CHMINACA),
including their optical, positional and
geometric isomers, salts, and salts of
isomers. The current final order
temporarily placing THJ–2201, AB–
PINACA and AB–CHMINACA into
schedule I is in effect through January
29, 2017. This order will extend the
temporary scheduling of THJ–2201, AB–
PINACA and AB–CHMINACA for one
year, or until the permanent scheduling
action for these three substances is
completed, whichever occurs first.
DATES: This temporary order is effective
January 27, 2017. This temporary order
will expire on January 29, 2018, or
when a permanent scheduling
proceeding is completed, whichever
occurs first.
FOR FURTHER INFORMATION CONTACT:
Michael J. Lewis, Diversion Control
Division, Drug Enforcement
Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia
22152; Telephone: (202) 598–6812.
SUPPLEMENTARY INFORMATION:
jstallworth on DSK7TPTVN1PROD with RULES
SUMMARY:
Legal Authority
The Drug Enforcement
Administration (DEA) implements and
enforces titles II and III of the
Comprehensive Drug Abuse Prevention
and Control Act of 1970, as amended.
Titles II and III are referred to as the
‘‘Controlled Substances Act’’ and the
‘‘Controlled Substances Import and
Export Act,’’ respectively, and are
collectively referred to as the
‘‘Controlled Substances Act’’ or the
‘‘CSA’’ for the purpose of this action. 21
U.S.C. 801–971. The DEA published the
implementing regulations for these
statutes in title 21 of the Code of Federal
Regulations (CFR), chapter II.
The CSA and its implementing
regulations are designed to prevent,
detect, and eliminate the diversion of
controlled substances and listed
chemicals into the illicit market while
ensuring an adequate supply is available
for the legitimate medical, scientific,
research, and industrial needs of the
United States. Controlled substances
have the potential for abuse and
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dependence and are controlled to
protect the public health and safety.
Under the CSA, every controlled
substance is classified into one of five
schedules based upon its potential for
abuse, its currently accepted medical
use in treatment in the United States,
and the degree of dependence the drug
or other substance may cause. 21 U.S.C.
812. The initial schedules of controlled
substances established by Congress are
found at 21 U.S.C. 812(c), and the
current list of all scheduled substances
is published at 21 CFR part 1308.
Section 201 of the CSA (21 U.S.C.
811) provides the Attorney General with
the authority to temporarily place a
substance into schedule I of the CSA for
two years without regard to the
requirements of 21 U.S.C. 811(b) if she
finds that such action is necessary to
avoid an imminent hazard to the public
safety. 21 U.S.C. 811(h)(1). In addition,
if proceedings to control a substance are
initiated under 21 U.S.C. 811(a)(1), the
Attorney General may extend the
temporary scheduling for up to one
year. 21 U.S.C. 811(h)(2).
Where the necessary findings are
made, a substance may be temporarily
scheduled if it is not listed in any other
schedule under section 202 of the CSA,
21 U.S.C. 812, or if there is no
exemption or approval in effect for the
substance under section 505 of the
Federal Food, Drug, and Cosmetic Act
(FDCA), 21 U.S.C. 355. 21 U.S.C.
811(h)(1). The Attorney General has
delegated her scheduling authority
under 21 U.S.C. 811 to the
Administrator of the DEA. 28 CFR
0.100.
Background
On January 30, 2015, the DEA
published a final order in the Federal
Register amending 21 CFR 1308.11(h) to
temporarily place the three synthetic
cannabinoids [1-(5-fluoropentyl)-1Hindazol-3-yl](naphthalen-1yl)methanone (THJ–2201); N-1-amino-3methyl-1-oxo-2-butanyl]-1-pentyl-1Hindazole-3-carboxamide (AB–PINACA);
and N-[1-amino-3-methyl-1-oxo-2butanyl]-1-(cyclohexylmethyl)-1Hindazole-3-carboxamide (AB–
CHMINACA) into schedule I of the CSA
pursuant to the temporary scheduling
provisions of 21 U.S.C. 811(h). 80 FR
5042. That final order was effective on
the date of publication, and was based
on findings by the Administrator of the
DEA that the temporary scheduling of
these three synthetic cannabinoids was
necessary to avoid an imminent hazard
to the public safety pursuant to 21
U.S.C. 811(h)(1). Section 201(h)(2) of the
CSA (21 U.S.C. 811(h)(2)) requires that
the temporary control of these
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8591
substances expires two years from the
effective date of the scheduling order, or
on January 29, 2017. However, the CSA
also provides that during the pendency
of proceedings under 21 U.S.C. 811(a)(1)
with respect to the substance, the
temporary scheduling of that substance
could be extended for up to one year.
Proceedings for the scheduling of a
substance under 21 U.S.C. 811(a) may
be initiated by the Attorney General
(delegated to the Administrator of the
DEA pursuant to 28 CFR 0.100) on his
or her own motion, at the request of the
Secretary of Health and Human
Services,1 or on the petition of any
interested party.
The Administrator of the DEA, on his
own motion pursuant to 21 U.S.C.
811(a), has initiated proceedings under
21 U.S.C. 811(a)(1) to permanently
schedule THJ–2201, AB–PINACA and
AB–CHMINACA. The DEA has gathered
and reviewed the available information
regarding the pharmacology, chemistry,
trafficking, actual abuse, pattern of
abuse, and the relative potential for
abuse for these three synthetic
cannabinoids. On August 26, 2015, the
DEA submitted a request to the HHS to
provide the DEA with a scientific and
medical evaluation of available
information and a scheduling
recommendation for THJ–2201, AB–
PINACA and AB–CHMINACA, in
accordance with 21 U.S.C. 811(b) and
(c). Upon evaluating the scientific and
medical evidence, on November 14,
2016, the HHS submitted to the
Administrator of the DEA its three
scientific and medical evaluations for
these substances. Upon receipt of the
scientific and medical evaluation and
scheduling recommendations from the
HHS, the DEA reviewed the documents
and all other relevant data, and
conducted its own eight-factor analysis
of the abuse potential of THJ–2201, AB–
PINACA and AB–CHMINACA in
accordance with 21 U.S.C. 811(c). The
DEA has published a notice of proposed
rulemaking for the placement of THJ–
2201, AB–PINACA and AB–
CHMINACA into schedule I elsewhere
in this issue of the Federal Register.
Pursuant to 21 U.S.C. 811(h)(2), the
Administrator of the DEA orders that
the temporary scheduling of THJ–2201,
AB–PINACA and AB–CHMINACA,
including their optical, positional and
geometric isomers, salts, and salts of
1 Because the Secretary of the Department of
Health and Human Services has delegated to the
Assistant Secretary for Health of the Department of
Health and Human Services the authority to make
domestic drug scheduling recommendations, for
purposes of this order, all subsequent references to
‘‘Secretary’’ have been replaced with ‘‘Assistant
Secretary.’’
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Federal Register / Vol. 82, No. 17 / Friday, January 27, 2017 / Rules and Regulations
isomers, be extended for one year, or
until the permanent scheduling
proceeding is completed, whichever
occurs first.
In accordance with this temporary
order, the schedule I requirements for
handling THJ–2201, AB–PINACA and
AB–CHMINACA, including their
optical, positional and geometric
isomers, salts, and salts of isomers, are
extended for one year, or until the
permanent scheduling proceeding is
completed, whichever occurs first.
jstallworth on DSK7TPTVN1PROD with RULES
Regulatory Matters
The CSA provides for an expedited
temporary scheduling action where
such action is necessary to avoid an
imminent hazard to the public safety. 21
U.S.C. 811(h). The Attorney General
may, by order, schedule a substance in
schedule I on a temporary basis. Id. 21
U.S.C. 811(h) also provides that the
temporary scheduling of a substance
shall expire at the end of two years from
the date of the issuance of the order
scheduling such substance, except that
the Attorney General may, during the
pendency of proceedings to
permanently schedule the substance,
extend the temporary scheduling for up
to one year.
To the extent that 21 U.S.C. 811(h)
directs that temporary scheduling
actions be issued by order and sets forth
the procedures by which such orders are
to be issued and extended, the DEA
believes that the notice and comment
requirements of section 553 of the
Administrative Procedure Act (APA) (5
U.S.C. 553) do not apply to this
extension of the temporary scheduling
action. In the alternative, even assuming
that this action might be subject to
section 553 of the APA, the
Administrator finds that there is good
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cause to forgo the notice and comment
requirements of section 553, as any
further delays in the process for
extending the temporary scheduling
order would be impracticable and
contrary to the public interest in view
of the manifest urgency to avoid an
imminent hazard to the public safety.
Further, the DEA believes that this order
extending the temporary scheduling
action is not a ‘‘rule’’ as defined by 5
U.S.C. 601(2), and, accordingly, is not
subject to the requirements of the
Regulatory Flexibility Act (RFA). The
requirements for the preparation of an
initial regulatory flexibility analysis in 5
U.S.C. 603(a) are not applicable where,
as here, the DEA is not required by
section 553 of the APA or any other law
to publish a general notice of proposed
rulemaking.
Additionally, this action is not a
significant regulatory action as defined
by Executive Order 12866 (Regulatory
Planning and Review), section 3(f), and,
accordingly, this action has not been
reviewed by the Office of Management
and Budget (OMB).
This action will not have substantial
direct effects on the States, on the
relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government. Therefore, in
accordance with Executive Order 13132
(Federalism) it is determined that this
action does not have sufficient
federalism implications to warrant the
preparation of a Federalism Assessment.
As noted above, this action is an
order, not a rule. Accordingly, the
Congressional Review Act (CRA) is
inapplicable, as it applies only to rules.
It is in the public interest to maintain
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the temporary placement of THJ–2201,
AB–PINACA and AB–CHMINACA in
schedule I because they pose a public
health risk. The temporary scheduling
action was taken pursuant to 21 U.S.C.
811(h), which is specifically designed to
enable the DEA to act in an expeditious
manner to avoid an imminent hazard to
the public safety. Under 21 U.S.C.
811(h), temporary scheduling orders are
not subject to notice and comment
rulemaking procedures. The DEA
understands that the CSA frames
temporary scheduling actions as orders
rather than rules to ensure that the
process moves swiftly, and this
extension of the temporary scheduling
order continues to serve that purpose.
For the same reasons that underlie 21
U.S.C. 811(h), that is, the need to place
these substances in schedule I because
they pose an imminent hazard to public
safety, it would be contrary to the public
interest to delay implementation of this
extension of the temporary scheduling
order. Therefore, in accordance with
section 808(2) of the CRA, this order
extending the temporary scheduling
order shall take effect immediately upon
its publication. The DEA has submitted
a copy of this temporary order to both
Houses of Congress and to the
Comptroller General, although such
filing is not required under the Small
Business Regulatory Enforcement
Fairness Act of 1996 (Congressional
Review Act) (5 U.S.C. 801–808) because,
as noted above, this action is an order,
not a rule.
Dated: January 17, 2017.
Chuck Rosenberg,
Acting Administrator.
[FR Doc. 2017–01517 Filed 1–26–17; 8:45 am]
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Agencies
[Federal Register Volume 82, Number 17 (Friday, January 27, 2017)]
[Rules and Regulations]
[Pages 8590-8592]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-01517]
=======================================================================
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA-402]
Schedules of Controlled Substances: Extension of Temporary
Placement of THJ-2201, AB-PINACA and AB-CHMINACA in Schedule I of the
Controlled Substances Act
AGENCY: Drug Enforcement Administration, Department of Justice.
ACTION: Temporary order.
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[[Page 8591]]
SUMMARY: The Administrator of the Drug Enforcement Administration is
issuing this temporary order to extend the temporary schedule I status
of three synthetic cannabinoids pursuant to the temporary scheduling
provisions of the Controlled Substances Act. The substances are: [1-(5-
Fluoropentyl)-1H-indazol-3-yl](naphthalen-1-yl)methanone (THJ-2201); N-
1-Amino-3-methyl-1-oxo-2-butanyl]-1-pentyl-1H-indazole-3-carboxamide
(AB-PINACA); N-[1-Amino-3-methyl-1-oxo-2-butanyl]-1-(cyclohexylmethyl)-
1H-indazole-3-carboxamide (AB-CHMINACA), including their optical,
positional and geometric isomers, salts, and salts of isomers. The
current final order temporarily placing THJ-2201, AB-PINACA and AB-
CHMINACA into schedule I is in effect through January 29, 2017. This
order will extend the temporary scheduling of THJ-2201, AB-PINACA and
AB-CHMINACA for one year, or until the permanent scheduling action for
these three substances is completed, whichever occurs first.
DATES: This temporary order is effective January 27, 2017. This
temporary order will expire on January 29, 2018, or when a permanent
scheduling proceeding is completed, whichever occurs first.
FOR FURTHER INFORMATION CONTACT: Michael J. Lewis, Diversion Control
Division, Drug Enforcement Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia 22152; Telephone: (202) 598-
6812.
SUPPLEMENTARY INFORMATION:
Legal Authority
The Drug Enforcement Administration (DEA) implements and enforces
titles II and III of the Comprehensive Drug Abuse Prevention and
Control Act of 1970, as amended. Titles II and III are referred to as
the ``Controlled Substances Act'' and the ``Controlled Substances
Import and Export Act,'' respectively, and are collectively referred to
as the ``Controlled Substances Act'' or the ``CSA'' for the purpose of
this action. 21 U.S.C. 801-971. The DEA published the implementing
regulations for these statutes in title 21 of the Code of Federal
Regulations (CFR), chapter II.
The CSA and its implementing regulations are designed to prevent,
detect, and eliminate the diversion of controlled substances and listed
chemicals into the illicit market while ensuring an adequate supply is
available for the legitimate medical, scientific, research, and
industrial needs of the United States. Controlled substances have the
potential for abuse and dependence and are controlled to protect the
public health and safety.
Under the CSA, every controlled substance is classified into one of
five schedules based upon its potential for abuse, its currently
accepted medical use in treatment in the United States, and the degree
of dependence the drug or other substance may cause. 21 U.S.C. 812. The
initial schedules of controlled substances established by Congress are
found at 21 U.S.C. 812(c), and the current list of all scheduled
substances is published at 21 CFR part 1308.
Section 201 of the CSA (21 U.S.C. 811) provides the Attorney
General with the authority to temporarily place a substance into
schedule I of the CSA for two years without regard to the requirements
of 21 U.S.C. 811(b) if she finds that such action is necessary to avoid
an imminent hazard to the public safety. 21 U.S.C. 811(h)(1). In
addition, if proceedings to control a substance are initiated under 21
U.S.C. 811(a)(1), the Attorney General may extend the temporary
scheduling for up to one year. 21 U.S.C. 811(h)(2).
Where the necessary findings are made, a substance may be
temporarily scheduled if it is not listed in any other schedule under
section 202 of the CSA, 21 U.S.C. 812, or if there is no exemption or
approval in effect for the substance under section 505 of the Federal
Food, Drug, and Cosmetic Act (FDCA), 21 U.S.C. 355. 21 U.S.C.
811(h)(1). The Attorney General has delegated her scheduling authority
under 21 U.S.C. 811 to the Administrator of the DEA. 28 CFR 0.100.
Background
On January 30, 2015, the DEA published a final order in the Federal
Register amending 21 CFR 1308.11(h) to temporarily place the three
synthetic cannabinoids [1-(5-fluoropentyl)-1H-indazol-3-yl](naphthalen-
1-yl)methanone (THJ-2201); N-1-amino-3-methyl-1-oxo-2-butanyl]-1-
pentyl-1H-indazole-3-carboxamide (AB-PINACA); and N-[1-amino-3-methyl-
1-oxo-2-butanyl]-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide (AB-
CHMINACA) into schedule I of the CSA pursuant to the temporary
scheduling provisions of 21 U.S.C. 811(h). 80 FR 5042. That final order
was effective on the date of publication, and was based on findings by
the Administrator of the DEA that the temporary scheduling of these
three synthetic cannabinoids was necessary to avoid an imminent hazard
to the public safety pursuant to 21 U.S.C. 811(h)(1). Section 201(h)(2)
of the CSA (21 U.S.C. 811(h)(2)) requires that the temporary control of
these substances expires two years from the effective date of the
scheduling order, or on January 29, 2017. However, the CSA also
provides that during the pendency of proceedings under 21 U.S.C.
811(a)(1) with respect to the substance, the temporary scheduling of
that substance could be extended for up to one year. Proceedings for
the scheduling of a substance under 21 U.S.C. 811(a) may be initiated
by the Attorney General (delegated to the Administrator of the DEA
pursuant to 28 CFR 0.100) on his or her own motion, at the request of
the Secretary of Health and Human Services,\1\ or on the petition of
any interested party.
---------------------------------------------------------------------------
\1\ Because the Secretary of the Department of Health and Human
Services has delegated to the Assistant Secretary for Health of the
Department of Health and Human Services the authority to make
domestic drug scheduling recommendations, for purposes of this
order, all subsequent references to ``Secretary'' have been replaced
with ``Assistant Secretary.''
---------------------------------------------------------------------------
The Administrator of the DEA, on his own motion pursuant to 21
U.S.C. 811(a), has initiated proceedings under 21 U.S.C. 811(a)(1) to
permanently schedule THJ-2201, AB-PINACA and AB-CHMINACA. The DEA has
gathered and reviewed the available information regarding the
pharmacology, chemistry, trafficking, actual abuse, pattern of abuse,
and the relative potential for abuse for these three synthetic
cannabinoids. On August 26, 2015, the DEA submitted a request to the
HHS to provide the DEA with a scientific and medical evaluation of
available information and a scheduling recommendation for THJ-2201, AB-
PINACA and AB-CHMINACA, in accordance with 21 U.S.C. 811(b) and (c).
Upon evaluating the scientific and medical evidence, on November 14,
2016, the HHS submitted to the Administrator of the DEA its three
scientific and medical evaluations for these substances. Upon receipt
of the scientific and medical evaluation and scheduling recommendations
from the HHS, the DEA reviewed the documents and all other relevant
data, and conducted its own eight-factor analysis of the abuse
potential of THJ-2201, AB-PINACA and AB-CHMINACA in accordance with 21
U.S.C. 811(c). The DEA has published a notice of proposed rulemaking
for the placement of THJ-2201, AB-PINACA and AB-CHMINACA into schedule
I elsewhere in this issue of the Federal Register.
Pursuant to 21 U.S.C. 811(h)(2), the Administrator of the DEA
orders that the temporary scheduling of THJ-2201, AB-PINACA and AB-
CHMINACA, including their optical, positional and geometric isomers,
salts, and salts of
[[Page 8592]]
isomers, be extended for one year, or until the permanent scheduling
proceeding is completed, whichever occurs first.
In accordance with this temporary order, the schedule I
requirements for handling THJ-2201, AB-PINACA and AB-CHMINACA,
including their optical, positional and geometric isomers, salts, and
salts of isomers, are extended for one year, or until the permanent
scheduling proceeding is completed, whichever occurs first.
Regulatory Matters
The CSA provides for an expedited temporary scheduling action where
such action is necessary to avoid an imminent hazard to the public
safety. 21 U.S.C. 811(h). The Attorney General may, by order, schedule
a substance in schedule I on a temporary basis. Id. 21 U.S.C. 811(h)
also provides that the temporary scheduling of a substance shall expire
at the end of two years from the date of the issuance of the order
scheduling such substance, except that the Attorney General may, during
the pendency of proceedings to permanently schedule the substance,
extend the temporary scheduling for up to one year.
To the extent that 21 U.S.C. 811(h) directs that temporary
scheduling actions be issued by order and sets forth the procedures by
which such orders are to be issued and extended, the DEA believes that
the notice and comment requirements of section 553 of the
Administrative Procedure Act (APA) (5 U.S.C. 553) do not apply to this
extension of the temporary scheduling action. In the alternative, even
assuming that this action might be subject to section 553 of the APA,
the Administrator finds that there is good cause to forgo the notice
and comment requirements of section 553, as any further delays in the
process for extending the temporary scheduling order would be
impracticable and contrary to the public interest in view of the
manifest urgency to avoid an imminent hazard to the public safety.
Further, the DEA believes that this order extending the temporary
scheduling action is not a ``rule'' as defined by 5 U.S.C. 601(2), and,
accordingly, is not subject to the requirements of the Regulatory
Flexibility Act (RFA). The requirements for the preparation of an
initial regulatory flexibility analysis in 5 U.S.C. 603(a) are not
applicable where, as here, the DEA is not required by section 553 of
the APA or any other law to publish a general notice of proposed
rulemaking.
Additionally, this action is not a significant regulatory action as
defined by Executive Order 12866 (Regulatory Planning and Review),
section 3(f), and, accordingly, this action has not been reviewed by
the Office of Management and Budget (OMB).
This action will not have substantial direct effects on the States,
on the relationship between the national government and the States, or
on the distribution of power and responsibilities among the various
levels of government. Therefore, in accordance with Executive Order
13132 (Federalism) it is determined that this action does not have
sufficient federalism implications to warrant the preparation of a
Federalism Assessment.
As noted above, this action is an order, not a rule. Accordingly,
the Congressional Review Act (CRA) is inapplicable, as it applies only
to rules. It is in the public interest to maintain the temporary
placement of THJ-2201, AB-PINACA and AB-CHMINACA in schedule I because
they pose a public health risk. The temporary scheduling action was
taken pursuant to 21 U.S.C. 811(h), which is specifically designed to
enable the DEA to act in an expeditious manner to avoid an imminent
hazard to the public safety. Under 21 U.S.C. 811(h), temporary
scheduling orders are not subject to notice and comment rulemaking
procedures. The DEA understands that the CSA frames temporary
scheduling actions as orders rather than rules to ensure that the
process moves swiftly, and this extension of the temporary scheduling
order continues to serve that purpose. For the same reasons that
underlie 21 U.S.C. 811(h), that is, the need to place these substances
in schedule I because they pose an imminent hazard to public safety, it
would be contrary to the public interest to delay implementation of
this extension of the temporary scheduling order. Therefore, in
accordance with section 808(2) of the CRA, this order extending the
temporary scheduling order shall take effect immediately upon its
publication. The DEA has submitted a copy of this temporary order to
both Houses of Congress and to the Comptroller General, although such
filing is not required under the Small Business Regulatory Enforcement
Fairness Act of 1996 (Congressional Review Act) (5 U.S.C. 801-808)
because, as noted above, this action is an order, not a rule.
Dated: January 17, 2017.
Chuck Rosenberg,
Acting Administrator.
[FR Doc. 2017-01517 Filed 1-26-17; 8:45 am]
BILLING CODE 4410-09-P