Proposed Adjustment of the Assessment of Annual Needs for the List I Chemicals Ephedrine, Pseudoephedrine, and Phenylpropanolamine for 2012, 42333-42334 [2012-17522]
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Federal Register / Vol. 77, No. 138 / Wednesday, July 18, 2012 / Notices
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Section, Environment and Natural Resources
Division.
[FR Doc. 2012–17417 Filed 7–17–12; 8:45 am]
BILLING CODE 4410–15–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–353]
Proposed Adjustment of the
Assessment of Annual Needs for the
List I Chemicals Ephedrine,
Pseudoephedrine, and
Phenylpropanolamine for 2012
Drug Enforcement
Administration (DEA), Department of
Justice.
ACTION: Notice with request for
comments.
AGENCY:
This notice proposes to adjust
the 2012 assessment of annual needs for
the list I chemicals ephedrine,
pseudoephedrine, and
phenylpropanolamine.
DATES: Electronic comments must be
submitted and written comments must
be postmarked on or before August 17,
2012. Commenters should be aware that
the electronic Federal Docket
Management System will not accept
comments after midnight Eastern Time
on the last day of the comment period.
ADDRESSES: To ensure proper handling
of comments, please reference ‘‘Docket
No. DEA–353’’ on all electronic and
written correspondence. DEA
encourages all comments be submitted
electronically through https://
www.regulations.gov using the
electronic comment form provided on
that site. An electronic copy of this
document is also available at the
https://www.regulations.gov Web site for
easy reference. Paper comments that
duplicate the electronic submission are
not necessary as all comments
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
17:27 Jul 17, 2012
Jkt 226001
submitted to www.regulations.gov will
be posted for public review and are part
of the official docket record. Should
you, however, wish to submit written
comments via regular or express mail,
they should be sent to the Drug
Enforcement Administration, Attention:
DEA Federal Register Representative/
ODL, 8701 Morrissette Drive,
Springfield, VA 22152.
FOR FURTHER INFORMATION CONTACT: John
W. Partridge, Chief, Liaison and Policy
Section, Drug Enforcement
Administration, 8701 Morrissette Drive,
Springfield, VA 22152, Telephone: (202)
307–4654.
SUPPLEMENTARY INFORMATION:
Posting of Public Comments
Please note that all comments
received are considered part of the
public record and made available for
public inspection online at https://
www.regulations.gov and in the DEA’s
public docket. Such information
includes personal identifying
information (such as your name,
address, etc.) voluntarily submitted by
the commenter.
If you want to submit personal
identifying information (such as your
name, address, etc.) as part of your
comment, but do not want it to be
posted online or made available in the
public docket, you must include the
phrase ‘‘PERSONAL IDENTIFYING
INFORMATION’’ in the first paragraph
of your comment. You must also place
all the personal identifying information
you do not want posted online or made
available in the public docket in the first
paragraph of your comment and identify
what information you want redacted.
If you want to submit confidential
business information as part of your
comment, but do not want it to be
posted online or made available in the
public docket, you must include the
phrase ‘‘CONFIDENTIAL BUSINESS
INFORMATION’’ in the first paragraph
of your comment. You must also
prominently identify confidential
business information to be redacted
within the comment. If a comment has
so much confidential business
information that it cannot be effectively
redacted, all or part of that comment
may not be posted online or made
available in the public docket.
Personal identifying information and
confidential business information
identified and located as set forth above
will be redacted, and the comment, in
redacted form, will be posted online and
placed in the DEA’s public docket file.
Please note that the Freedom of
Information Act applies to all comments
received. If you wish to inspect the
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
42333
agency’s public docket file in person by
appointment, please see the FOR
FURTHER INFORMATION CONTACT
paragraph.
Background
On December 12, 2011, DEA
established the assessment of annual
needs for 2012 for the list I chemicals
ephedrine, pseudoephedrine, and
phenylpropanolamine, pursuant to 21
U.S.C. 826(a) and 21 CFR 1315.11 (76
FR 77252). That Notice indicated that
DEA would adjust the assessment of
annual needs at a later date, if
necessary, as provided in 21 CFR
1315.13.
DEA now proposes to adjust the
established assessment of annual needs
for 2012 for the list I chemicals
ephedrine, pseudoephedrine, and
phenylpropanolamine. In proposing the
adjustment, DEA has taken into account
the criteria that DEA is required to
consider in accordance with 21 CFR
1315.13. DEA proposes the adjustment
of the assessment of annual needs for
2012 by considering: (1) Changes in
demand, changes in the national rate of
net disposal, and changes in the rate of
net disposal by the registrants holding
individual manufacturing or import
quotas for the chemical; (2) whether any
increased demand or changes in the
national and/or individual rates of net
disposal are temporary, short term, or
long term; (3) whether any increased
demand can be met through existing
inventories, increased individual
manufacturing quotas, or increased
importation without increasing the
assessment of annual needs; (4) whether
any decreased demand will result in
excessive inventory accumulation by all
persons registered to handle the
particular chemical; and (5) other
factors affecting the medical, scientific,
research, industrial, and importation
needs in the United States, lawful
export requirements, and reserve stocks,
as the Administrator finds relevant.
Other factors that DEA considered
include trends as derived from
information provided in applications for
import, manufacturing, and
procurement quotas and in import and
export declarations. The inventory,
acquisition (purchases), and disposition
(sales) data as provided by DEA
registered manufacturers and importers
reflects the most current information
available to DEA at the time of
publication of this Notice.
Analysis
In determining whether to propose
adjustments to the 2012 assessment of
annual needs, DEA considered the total
net disposals (i.e., sales) of the list I
E:\FR\FM\18JYN1.SGM
18JYN1
42334
Federal Register / Vol. 77, No. 138 / Wednesday, July 18, 2012 / Notices
chemicals for the current and preceding
two years, actual and estimated
inventories, projected demand (2012),
industrial use, and export requirements
from updated data provided by DEA
registered manufacturers and importers
in procurement quota applications (DEA
250), manufacturing quota applications
(DEA 189), import quota applications
(DEA 488), declarations for import and
export, and other information. Data
considered included data submitted to
DEA after the initial assessment of
annual needs had been established. DEA
notes that the inventory, acquisition
(purchases), and disposition (sales) data
proved by DEA registered manufacturers
and importers reflects the most current
information available. In developing the
proposed 2012 revision, DEA has used
the calculation methodology described
previously in the 2010 and 2011
assessment of annual needs (74 FR
60294 and 75 FR 79407, respectively).
As of June 6, 2012, DEA registered
manufacturers of dosage form products
containing pseudoephedrine requested
quota for 322,385 kg of
pseudoephedrine. DEA registered
manufacturers of pseudoephedrine
reported sales totaling approximately
189,030 kg in 2010 and 268,669 kg in
2011; this represents a 30 percent
increase in sales reported by these firms
from 2010 to 2011. Additionally, DEA
considered information on trends in the
national rate of net disposals from sales
data provided by IMS Health. The initial
assessment of annual needs was based
on data received by DEA as of October
17, 2011. Based on the updated
information provided to DEA as of June
6, 2012, DEA is proposing to increase
the 2011 assessment of annual needs for
pseudoephedrine from 258,000 kg to
278,000 kg.
As of June 6, 2012, DEA registered
manufacturers of dosage form products
containing ephedrine requested quota
for 4,221 kg of ephedrine (for sale) in
2012. DEA registered manufacturers of
ephedrine reported sales totaling
approximately 1,598 kg in 2010 and
3,158 kg in 2011; this represents a 49
percent increase in sales reported by
these firms from 2010 to 2011.
Additionally, DEA considered
information on trends in the national
rate of net disposals from sales data
provided by IMS Health. The initial
assessment of annual needs was based
on data received by DEA as of October
17, 2011. Based on the updated
information provided to DEA as of June
6, 2012, DEA is proposing to increase
the 2012 assessment of annual needs for
ephedrine (for sale) from 4,000 kg to
4,300 kg.
As of June 6, 2012, DEA registered
manufacturers of phenylpropanolamine
(for sale) requested quota for 7,763 kg of
phenylpropanolamine (for sale). DEA
registered manufacturers of
phenylpropanolamine reported sales
totaling approximately 4,790 kg in 2010
and 5,289 kg in 2011; this represents a
nine percent increase in sales reported
by these firms from 2010 to 2011. DEA
notes that phenylpropanolamine is sold
primarily as a veterinary product and is
not approved for human consumption.
IMS Health’s NSP Data does not capture
sales of phenylpropanolamine to
veterinary channels and is, therefore,
not considered. The initial assessment
of annual needs was based on data
received by DEA as of October 17, 2011.
DEA is proposing to increase the 2012
assessment of annual needs for
phenylpropanolamine (for sale) from
5,200 kg to 5,800 kg.
As of June 6, 2012, the data provided
to DEA for review of
phenylpropanolamine (for conversion)
and ephedrine (for conversion)
demonstrated no significant changes in
demand or net disposals. DEA has thus
determined that the assessment of
annual needs for these chemicals—
phenylpropanolamine (for conversion)
and ephedrine (for conversion)—shall
remain unchanged.
The Administrator, therefore,
proposes the following adjustment of
the 2012 assessment of annual needs for
the list I chemicals ephedrine,
pseudoephedrine, and
phenylpropanolamine as follows:
2012 assessment of annual
needs
(kg)
List I chemicals
Ephedrine (for sale) .................................................................................................................................................
Phenylpropanolamine (for sale) ...............................................................................................................................
Pseudoephedrine .....................................................................................................................................................
Phenylpropanolamine (for conversion) ....................................................................................................................
Ephedrine (for conversion) ......................................................................................................................................
tkelley on DSK3SPTVN1PROD with NOTICES
In finalizing the adjustment of the
2012 assessment of annual needs for
ephedrine, pseudoephedrine, and
phenylpropanolamine, DEA will
consider any additional changes in
demand, changes in the national rate of
net disposal, or changes in the rate of
net disposal by the registrants holding
individual manufacturing or import
quotas for the chemical, in accordance
with 21 CFR Part 1315.
Comments
Pursuant to 21 CFR 1315.13, any
interested person may submit written
comments on or objections to these
proposed determinations. Based on
comments received in response to this
Notice, the Administrator may hold a
VerDate Mar<15>2010
17:27 Jul 17, 2012
Jkt 226001
Proposed adjustment to the
2012 assessment of annual
needs (kg)
4,000
5,200
258,000
26,200
12,000
4,300
5,800
278,000
No Change
No Change
public hearing on one or more issues
raised. In the event the Administrator
decides in her sole discretion to hold
such a hearing, the Administrator will
publish a notice of any such hearing in
the Federal Register. After
consideration of any comments and
after a hearing, if one is held, the
Administrator will publish in the
Federal Register a Final Order
determining any adjustment of the
assessment of annual needs.
DEPARTMENT OF JUSTICE
Dated: July 13, 2012.
Michele M. Leonhart,
Administrator.
SUMMARY:
[FR Doc. 2012–17522 Filed 7–17–12; 8:45 am]
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Office of Justice Programs
[OJP (OJJDP) Docket No. 1596]
Meeting of the Attorney General’s
National Task Force on Children
Exposed to Violence (Correction)
Office of Justice Programs,
Justice.
ACTION: Notice; correction.
AGENCY:
The Office of Justice Programs
(OJP) published a notice in the Federal
Register on July 2, 2012, announcing a
meeting of the Attorney General’s
National Task Force on Children
Exposed to Violence (the ‘‘task force’’).
As that notice stated, the final agenda
E:\FR\FM\18JYN1.SGM
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Agencies
[Federal Register Volume 77, Number 138 (Wednesday, July 18, 2012)]
[Notices]
[Pages 42333-42334]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-17522]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-353]
Proposed Adjustment of the Assessment of Annual Needs for the
List I Chemicals Ephedrine, Pseudoephedrine, and Phenylpropanolamine
for 2012
AGENCY: Drug Enforcement Administration (DEA), Department of Justice.
ACTION: Notice with request for comments.
-----------------------------------------------------------------------
SUMMARY: This notice proposes to adjust the 2012 assessment of annual
needs for the list I chemicals ephedrine, pseudoephedrine, and
phenylpropanolamine.
DATES: Electronic comments must be submitted and written comments must
be postmarked on or before August 17, 2012. Commenters should be aware
that the electronic Federal Docket Management System will not accept
comments after midnight Eastern Time on the last day of the comment
period.
ADDRESSES: To ensure proper handling of comments, please reference
``Docket No. DEA-353'' on all electronic and written correspondence.
DEA encourages all comments be submitted electronically through https://www.regulations.gov using the electronic comment form provided on that
site. An electronic copy of this document is also available at the
https://www.regulations.gov Web site for easy reference. Paper comments
that duplicate the electronic submission are not necessary as all
comments submitted to www.regulations.gov will be posted for public
review and are part of the official docket record. Should you, however,
wish to submit written comments via regular or express mail, they
should be sent to the Drug Enforcement Administration, Attention: DEA
Federal Register Representative/ODL, 8701 Morrissette Drive,
Springfield, VA 22152.
FOR FURTHER INFORMATION CONTACT: John W. Partridge, Chief, Liaison and
Policy Section, Drug Enforcement Administration, 8701 Morrissette
Drive, Springfield, VA 22152, Telephone: (202) 307-4654.
SUPPLEMENTARY INFORMATION:
Posting of Public Comments
Please note that all comments received are considered part of the
public record and made available for public inspection online at https://www.regulations.gov and in the DEA's public docket. Such information
includes personal identifying information (such as your name, address,
etc.) voluntarily submitted by the commenter.
If you want to submit personal identifying information (such as
your name, address, etc.) as part of your comment, but do not want it
to be posted online or made available in the public docket, you must
include the phrase ``PERSONAL IDENTIFYING INFORMATION'' in the first
paragraph of your comment. You must also place all the personal
identifying information you do not want posted online or made available
in the public docket in the first paragraph of your comment and
identify what information you want redacted.
If you want to submit confidential business information as part of
your comment, but do not want it to be posted online or made available
in the public docket, you must include the phrase ``CONFIDENTIAL
BUSINESS INFORMATION'' in the first paragraph of your comment. You must
also prominently identify confidential business information to be
redacted within the comment. If a comment has so much confidential
business information that it cannot be effectively redacted, all or
part of that comment may not be posted online or made available in the
public docket.
Personal identifying information and confidential business
information identified and located as set forth above will be redacted,
and the comment, in redacted form, will be posted online and placed in
the DEA's public docket file. Please note that the Freedom of
Information Act applies to all comments received. If you wish to
inspect the agency's public docket file in person by appointment,
please see the FOR FURTHER INFORMATION CONTACT paragraph.
Background
On December 12, 2011, DEA established the assessment of annual
needs for 2012 for the list I chemicals ephedrine, pseudoephedrine, and
phenylpropanolamine, pursuant to 21 U.S.C. 826(a) and 21 CFR 1315.11
(76 FR 77252). That Notice indicated that DEA would adjust the
assessment of annual needs at a later date, if necessary, as provided
in 21 CFR 1315.13.
DEA now proposes to adjust the established assessment of annual
needs for 2012 for the list I chemicals ephedrine, pseudoephedrine, and
phenylpropanolamine. In proposing the adjustment, DEA has taken into
account the criteria that DEA is required to consider in accordance
with 21 CFR 1315.13. DEA proposes the adjustment of the assessment of
annual needs for 2012 by considering: (1) Changes in demand, changes in
the national rate of net disposal, and changes in the rate of net
disposal by the registrants holding individual manufacturing or import
quotas for the chemical; (2) whether any increased demand or changes in
the national and/or individual rates of net disposal are temporary,
short term, or long term; (3) whether any increased demand can be met
through existing inventories, increased individual manufacturing
quotas, or increased importation without increasing the assessment of
annual needs; (4) whether any decreased demand will result in excessive
inventory accumulation by all persons registered to handle the
particular chemical; and (5) other factors affecting the medical,
scientific, research, industrial, and importation needs in the United
States, lawful export requirements, and reserve stocks, as the
Administrator finds relevant.
Other factors that DEA considered include trends as derived from
information provided in applications for import, manufacturing, and
procurement quotas and in import and export declarations. The
inventory, acquisition (purchases), and disposition (sales) data as
provided by DEA registered manufacturers and importers reflects the
most current information available to DEA at the time of publication of
this Notice.
Analysis
In determining whether to propose adjustments to the 2012
assessment of annual needs, DEA considered the total net disposals
(i.e., sales) of the list I
[[Page 42334]]
chemicals for the current and preceding two years, actual and estimated
inventories, projected demand (2012), industrial use, and export
requirements from updated data provided by DEA registered manufacturers
and importers in procurement quota applications (DEA 250),
manufacturing quota applications (DEA 189), import quota applications
(DEA 488), declarations for import and export, and other information.
Data considered included data submitted to DEA after the initial
assessment of annual needs had been established. DEA notes that the
inventory, acquisition (purchases), and disposition (sales) data proved
by DEA registered manufacturers and importers reflects the most current
information available. In developing the proposed 2012 revision, DEA
has used the calculation methodology described previously in the 2010
and 2011 assessment of annual needs (74 FR 60294 and 75 FR 79407,
respectively).
As of June 6, 2012, DEA registered manufacturers of dosage form
products containing pseudoephedrine requested quota for 322,385 kg of
pseudoephedrine. DEA registered manufacturers of pseudoephedrine
reported sales totaling approximately 189,030 kg in 2010 and 268,669 kg
in 2011; this represents a 30 percent increase in sales reported by
these firms from 2010 to 2011. Additionally, DEA considered information
on trends in the national rate of net disposals from sales data
provided by IMS Health. The initial assessment of annual needs was
based on data received by DEA as of October 17, 2011. Based on the
updated information provided to DEA as of June 6, 2012, DEA is
proposing to increase the 2011 assessment of annual needs for
pseudoephedrine from 258,000 kg to 278,000 kg.
As of June 6, 2012, DEA registered manufacturers of dosage form
products containing ephedrine requested quota for 4,221 kg of ephedrine
(for sale) in 2012. DEA registered manufacturers of ephedrine reported
sales totaling approximately 1,598 kg in 2010 and 3,158 kg in 2011;
this represents a 49 percent increase in sales reported by these firms
from 2010 to 2011. Additionally, DEA considered information on trends
in the national rate of net disposals from sales data provided by IMS
Health. The initial assessment of annual needs was based on data
received by DEA as of October 17, 2011. Based on the updated
information provided to DEA as of June 6, 2012, DEA is proposing to
increase the 2012 assessment of annual needs for ephedrine (for sale)
from 4,000 kg to 4,300 kg.
As of June 6, 2012, DEA registered manufacturers of
phenylpropanolamine (for sale) requested quota for 7,763 kg of
phenylpropanolamine (for sale). DEA registered manufacturers of
phenylpropanolamine reported sales totaling approximately 4,790 kg in
2010 and 5,289 kg in 2011; this represents a nine percent increase in
sales reported by these firms from 2010 to 2011. DEA notes that
phenylpropanolamine is sold primarily as a veterinary product and is
not approved for human consumption. IMS Health's NSP Data does not
capture sales of phenylpropanolamine to veterinary channels and is,
therefore, not considered. The initial assessment of annual needs was
based on data received by DEA as of October 17, 2011. DEA is proposing
to increase the 2012 assessment of annual needs for phenylpropanolamine
(for sale) from 5,200 kg to 5,800 kg.
As of June 6, 2012, the data provided to DEA for review of
phenylpropanolamine (for conversion) and ephedrine (for conversion)
demonstrated no significant changes in demand or net disposals. DEA has
thus determined that the assessment of annual needs for these
chemicals--phenylpropanolamine (for conversion) and ephedrine (for
conversion)--shall remain unchanged.
The Administrator, therefore, proposes the following adjustment of
the 2012 assessment of annual needs for the list I chemicals ephedrine,
pseudoephedrine, and phenylpropanolamine as follows:
------------------------------------------------------------------------
Proposed
2012 adjustment to
assessment of the 2012
List I chemicals annual needs assessment of
(kg) annual needs
(kg)
------------------------------------------------------------------------
Ephedrine (for sale).................... 4,000 4,300
Phenylpropanolamine (for sale).......... 5,200 5,800
Pseudoephedrine......................... 258,000 278,000
Phenylpropanolamine (for conversion).... 26,200 No Change
Ephedrine (for conversion).............. 12,000 No Change
------------------------------------------------------------------------
In finalizing the adjustment of the 2012 assessment of annual needs
for ephedrine, pseudoephedrine, and phenylpropanolamine, DEA will
consider any additional changes in demand, changes in the national rate
of net disposal, or changes in the rate of net disposal by the
registrants holding individual manufacturing or import quotas for the
chemical, in accordance with 21 CFR Part 1315.
Comments
Pursuant to 21 CFR 1315.13, any interested person may submit
written comments on or objections to these proposed determinations.
Based on comments received in response to this Notice, the
Administrator may hold a public hearing on one or more issues raised.
In the event the Administrator decides in her sole discretion to hold
such a hearing, the Administrator will publish a notice of any such
hearing in the Federal Register. After consideration of any comments
and after a hearing, if one is held, the Administrator will publish in
the Federal Register a Final Order determining any adjustment of the
assessment of annual needs.
Dated: July 13, 2012.
Michele M. Leonhart,
Administrator.
[FR Doc. 2012-17522 Filed 7-17-12; 8:45 am]
BILLING CODE 4410-09-P