Manufacturer of Controlled Substances Notice of Application, 4828-4829 [2012-1975]
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4828
Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
Summary of Information Collection
DEPARTMENT OF JUSTICE
(1) Type of Information Collection:
Revision of a currently approved
collection.
(2) Title of the Form/Collection: FFL
Out-of-Business Records Request.
(3) Agency form number, if any, and
the applicable component of the
Department of Justice sponsoring the
collection: Form Number: ATF F
5300.3A. Bureau of Alcohol, Tobacco,
Firearms and Explosives.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Business or other forprofit. Other: None.
Bureau of Alcohol, Tobacco, Firearms
and Explosives
Need for Collection
Firearms licensees are required to
keep records of acquisition and
disposition. These records remain with
the licensee as long as they are in
business. The ATF F 5300.3A, FFL Outof-Business Records Request is used by
ATF to notify licensees who go out of
business. When discontinuance of the
business is absolute, such records shall
be delivered within thirty days
following the business discontinuance
to the ATF Out-of-Business Records
Center.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: It is estimated that 2,285
respondents will take approximately 5
minutes to complete the form.
(6) An estimate of the total public
burden (in hours) associated with the
collection: There are an estimated 190.4
annual total burden hours associated
with this collection.
If additional information is required
contact: Jerri Murray, Department
Clearance Officer, Policy and Planning
Staff, Justice Management Division,
Department of Justice, Two Constitution
Square, Room 2E–508, 145th Street NE.,
Washington, DC 20530.
Jerri Murray,
Department Clearance Officer, PRA, U.S.
Department of Justice.
[FR Doc. 2012–2030 Filed 1–30–12; 8:45 am]
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Agency Information Collection
Activities: Proposed Collection;
Comments Requested: Firearms
Disabilities for Nonimmigrant Aliens
The last notification was filed with
the Department on April 4, 2011. A
notice was published in the Federal
Register pursuant to Section 6(b) of the
Act on April 28, 2011 (76 FR 23839).
Patricia A. Brink,
Director of Civil Enforcement, Antitrust
Division.
[FR Doc. 2012–2041 Filed 1–30–12; 8:45 am]
BILLING CODE P
Correction
In notice document 2012–1057
appearing on page 3006 in the issue of
Friday, January 20, 2012 make the
following correction:
In the first column, in the next to last
paragraph, starting in the third line
‘‘[insert the date 30 days from the date
this notice is published in the Federal
Register]’’ should read ‘‘February 21,
2012’’.
[FR Doc. C1–2012–1057 Filed 1–30–12; 8:45 am]
BILLING CODE 1505–01–P
DEPARTMENT OF JUSTICE
Antitrust Division
Notice Pursuant to the National
Cooperative Research and Production
Act of 1993—OPENSAF Foundation
Notice is hereby given that, on
January 4, 2012, pursuant to Section 6(a)
of the National Cooperative Research
and Production Act of 1993, 15 U.S.C.
4301 et seq. (‘‘the Act’’), OpenSAF
Foundation has filed written
notifications simultaneously with the
Attorney General and the Federal Trade
Commission disclosing changes in its
membership. The notifications were
filed for the purpose of extending the
Act’s provisions limiting the recovery of
antitrust plaintiffs to actual damages
under specified circumstances.
Specifically, GoAhead Software,
Bellevue, WA; and Huawei Industrial
Base, Shenzhen, Guangdong, PEOPLE’S
REPUBLIC OF CHINA, have withdrawn
as parties to this venture.
No other changes have been made in
either the membership or planned
activity of the group research project.
Membership in this group research
project remains open, and OpenSAF
Foundation intends to file additional
written notifications disclosing all
changes in membership.
On April 8, 2008, OpenSAF
Foundation filed its original notification
pursuant to Section 6(a) of the Act. The
Department of Justice published a notice
in the Federal Register pursuant to
Section 6(b) of the Act on May 16, 2008
(73 FR 28508).
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances Notice of Application
Pursuant to § 1301.33(a), Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on November 7, 2011,
Mallinckrodt, LLC, 3600 North Second
Street, St. Louis, Missouri 63147, made
application by renewal to the Drug
Enforcement Administration (DEA) to
be registered as a bulk manufacturer of
the following basic classes of controlled
substances:
Drug
Tetrahydrocannabinols (7370) .....
Codeine-N-oxide (9053) ...............
Dihydromorphine (9145) ...............
Difenoxin (9168) ...........................
Morphine-N-oxide (9307) .............
Normorphine (9313) .....................
Norlevorphanol (9634) ..................
Amphetamine (1100) ....................
Methamphetamine (1105) ............
Methylphenidate (1724) ................
Nabilone (7379) ............................
4-Anilino-N-phenethyl-4-piperidine
(8333).
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Diphenoxylate (9170) ...................
Ecgonine (9180) ...........................
Hydrocodone (9193) .....................
Levorphanol (9220) ......................
Meperidine (9230) ........................
Methadone (9250) ........................
Methadone intermediate (9254) ...
Metopon (9260) ............................
Dextropropoxyphene, bulk.
(non-dosage forms) (9273) ..........
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Opium tincture (9630) ..................
Opium, powdered (9639) .............
Oxymorphone (9652) ...................
Noroxymorphone (9668) ..............
Alfentanil (9737) ...........................
Remifentanil (9739) ......................
Sufentanil (9740) ..........................
Fentanyl (9801) ............................
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Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
The firm plans to manufacture the
listed controlled substances for internal
use and for sale to other companies.
Any other such applicant, and any
person who is presently registered with
DEA to manufacture such substances,
may file comments or objections to the
issuance of the proposed registration
pursuant to 21 CFR 1301.33(a).
Any such written comments or
objections should be addressed, in
quintuplicate, to the Drug Enforcement
Administration, Office of Diversion
Control, Federal Register Representative
(ODL), 8701 Morrissette Drive,
Springfield, Virginia 22152; and must be
filed no later than April 2, 2012.
Dated: January 23, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2012–1975 Filed 1–30–12; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
wreier-aviles on DSK5TPTVN1PROD with NOTICES
Emilio Luna, M.D.; Decision and Order
On July 12, 2011, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Emilio Luna, M.D.
(Registrant), of Phoenix, Arizona. The
Show Cause Order proposed the
revocation of Registrant’s DEA
Certificate of Registration as a
practitioner, on the grounds that he does
not possess authority to handle
controlled substances in Arizona, the
State in which he is registered with
DEA, and that his continued registration
is inconsistent with the public interest.
Show Cause Order at 1 (citing 21 U.S.C.
824(a)(3) & (4)).
More specifically, the Show Cause
Order alleged that on September 1,
2010, the Federal Bureau of
Investigation arrested and charged
Registrant with distributing child
pornography in interstate commerce. Id.
The Order further alleged that on
September 3, 2010, the Arizona Medical
Board issued an Interim Order for
Practice Restriction and Consent Order,
under which Registrant is prohibited
‘‘from prescribing any form of treatment
including prescription medications.’’ Id.
The Show Cause Order also notified
Registrant of his right to request a
hearing on the allegations or to submit
a written statement in lieu of a hearing,
the procedures for doing either, and the
consequence for failing to do either. Id.
at 2 (citing 21 CFR 1301.43).
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The Government initially attempted
to serve the Show Cause Order on
Registrant by certified mail, return
receipt requested, addressed to him at
his registered location. However, the
mailing was returned to the Agency and
stamped ‘‘Returned to Sender
Attempted Not Known’’; in addition, the
word ‘‘Refused’’ was handwritten on the
envelope. GX 4. Simultaneously, the
Show Cause Order was emailed to
Registrant at the email address he had
previously provided to the Agency. GX
5. Thereafter, the Government did not
receive back either an error or
undeliverable message. See Gov.
Statement Re: Service of the Order to
Show Cause. In addition, several weeks
later, Diversion Investigators attempted
to personally serve Registrant at his
registered location. GX 6, at 1. However,
the DIs were told that Registrant ‘‘was
not present and no longer practices at
the clinic.’’ Id.
Before proceeding to the merits, it is
necessary to determine whether the
means employed by the Government to
serve the Show Cause Order on
Registrant were constitutionally
sufficient. The Supreme Court has long
held ‘‘that due process requires the
government to provide ‘notice
reasonably calculated, under all the
circumstances, to apprise interested
parties of the pendency of the action
and afford them an opportunity to
present their objections.’ ’’ Jones v.
Flowers, 547 U.S. 220, 226 (2006)
(quoting Mullane v. Central Hanover
Bank & Trust Co., 339 U.S. 306, 314
(1950)). Moreover, ‘‘ ‘when notice is a
person’s due * * * [t]he means
employed must be such as one desirous
of actually informing the absentee might
reasonably adopt to accomplish it.’ ’’
Jones, 547 U.S. at 229 (quoting Mullane,
339 U.S. at 315).
In Jones, the Court further noted that
its cases ‘‘require[] the government to
consider unique information about an
intended recipient regardless of whether
a statutory scheme is reasonably
calculated to provide notice in the
ordinary case.’’ Id. at 230. The Court
cited with approval its decision in
Robinson v. Hanrahan, 409 U.S. 38
(1972), where it ‘‘held that notice of
forfeiture proceedings sent to a vehicle
owner’s home address was inadequate
when the State knew that the property
owner was in prison.’’ Jones, 547 U.S.
at 230.1 See also Robinson, 409 U.S. at
1 The CSA states that ‘‘[b]efore taking action
pursuant to [21 U.S.C. 824(a)] * * * the Attorney
General shall serve upon the * * * registrant an
order to show cause why registration should not be
* * * revoked[] or suspended.’’ 21 U.S.C. 824(c). In
contrast to the schemes challenged in Jones and
Robinson, which provided for service to the
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4829
40 (‘‘[T]he State knew that appellant
was not at the address to which the
notice was mailed * * * since he was
at that very time confined in * * * jail.
Under these circumstances, it cannot be
said that the State made any effort to
provide notice which was ‘reasonably
calculated’ to apprise appellant of the
pendency of the * * * proceedings.’’);
Covey v. Town of Somers, 351 U.S. 141
(1956) (holding that notice by mailing,
publication, and posting was inadequate
when officials knew that recipient was
incompetent).
The Jones Court further explained that
‘‘under Robinson and Covey, the
government’s knowledge that notice
pursuant to the normal procedure was
ineffective triggered an obligation on the
government’s part to take additional
steps to effect notice.’’ 547 U.S. at 230.
The Court also noted that ‘‘a party’s
ability to take steps to safeguard its own
interests [such as by updating his
address] does not relieve the State of its
constitutional obligation.’’ Id. at 232
(quoting Brief for United States as
Amicus Curiae 16 n.5 (quoting
Mennonite Bd. of Missions v. Adams,
462 U.S. 791, 799 (1983))). However, the
Government is not required to
undertake ‘‘heroic efforts’’ to find a
registrant. Dusenbery v. United States,
534 U.S. 161, 170 (2002). Nor is actual
notice required. Id.
Thus, in Jones, the Court held that
where the State had received back a
certified mailing of process as
unclaimed and took ‘‘no further action’’
to notify the property owner, the State
did not satisfy due process. 547 U.S. at
230. Rather, the State was required to
‘‘take further reasonable steps if any
were available.’’ Id.
I conclude that the Government has
satisfied its obligation under the Due
Process Clause ‘‘to provide ‘notice
reasonably calculated, under all the
circumstances, to apprise interested
parties of the pendency of the action
and afford them an opportunity to
present their objections.’ ’’ Id. at 226
(quoting Mullane, 339 U.S. at 314). Even
assuming that the Government’s
attempts to serve Registrant by certified
mail and personal service 2 did not
property owner’s address as listed in state records,
neither the CSA nor Agency regulations state that
service shall be made at any particular address such
as the registered location. In any event, while in
most cases, service to a registrant’s registered
location provides adequate notice, the Supreme
Court’s clear instruction is that the Government
cannot ignore ‘‘unique information about an
intended recipient’’ when its seeks to serve that
person with notice of a proceeding that it is
initiating. Jones, 547 U.S. at 230.
2 As for the use of mail, after Jones, it seems
relatively clear that when certified mail is returned
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Agencies
[Federal Register Volume 77, Number 20 (Tuesday, January 31, 2012)]
[Notices]
[Pages 4828-4829]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-1975]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances Notice of Application
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal
Regulations (CFR), this is notice that on November 7, 2011,
Mallinckrodt, LLC, 3600 North Second Street, St. Louis, Missouri 63147,
made application by renewal to the Drug Enforcement Administration
(DEA) to be registered as a bulk manufacturer of the following basic
classes of controlled substances:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)............... I
Codeine-N-oxide (9053)..................... I
Dihydromorphine (9145)..................... I
Difenoxin (9168)........................... I
Morphine-N-oxide (9307).................... I
Normorphine (9313)......................... I
Norlevorphanol (9634)...................... I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Methylphenidate (1724)..................... II
Nabilone (7379)............................ II
4-Anilino-N-phenethyl-4-piperidine (8333).. II
Codeine (9050)............................. II
Dihydrocodeine (9120)...................... II
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Diphenoxylate (9170)....................... II
Ecgonine (9180)............................ II
Hydrocodone (9193)......................... II
Levorphanol (9220)......................... II
Meperidine (9230).......................... II
Methadone (9250)........................... II
Methadone intermediate (9254).............. II
Metopon (9260)............................. II
Dextropropoxyphene, bulk...................
(non-dosage forms) (9273).................. II
Morphine (9300)............................ II
Oripavine (9330)........................... II
Thebaine (9333)............................ II
Opium tincture (9630)...................... II
Opium, powdered (9639)..................... II
Oxymorphone (9652)......................... II
Noroxymorphone (9668)...................... II
Alfentanil (9737).......................... II
Remifentanil (9739)........................ II
Sufentanil (9740).......................... II
Fentanyl (9801)............................ II
------------------------------------------------------------------------
[[Page 4829]]
The firm plans to manufacture the listed controlled substances for
internal use and for sale to other companies.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substances, may file comments
or objections to the issuance of the proposed registration pursuant to
21 CFR 1301.33(a).
Any such written comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than April 2, 2012.
Dated: January 23, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-1975 Filed 1-30-12; 8:45 am]
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