Substances Prohibited From Use in Animal Food or Feed; Confirmation of Effective Date of Final Rule; Correction, 20583 [E9-10138]
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Federal Register / Vol. 74, No. 85 / Tuesday, May 5, 2009 / Rules and Regulations
‘‘Substances Prohibited From Use in
Animal Food or Feed’’ (referred to
herein as the April 25, 2008, final rule),
that would become effective 1 year after
that publication.’’
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 589
Dated: April 28, 2009.
Jeffrey Shuren,
Associate Commissioner for Policy and
Planning.
[FR Doc. E9–10138 Filed 5–4–09; 8:45 am]
[Docket No. FDA–2002–N–0031] (formerly
Docket No. 2002N–0273)
RIN 0910–AF46
Substances Prohibited From Use in
Animal Food or Feed; Confirmation of
Effective Date of Final Rule; Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION: Final rule; confirmation of
effective date; correction.
VerDate Nov<24>2008
22:59 May 04, 2009
Jkt 217001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
The Food and Drug
Administration (FDA) is correcting a
final rule; confirmation of effective date,
that appeared in the Federal Register of
Friday, April 24, 2009 (74 FR 18626)
(the April 24, 2009, final rule;
confirmation of effective date). That
document had confirmed the effective
date of April 27, 2009, for a final rule
that published in the Federal Register of
April 25, 2008 (73 FR 22720), entitled
‘‘Substances Prohibited From Use in
Animal Food or Feed.’’ In the April 24,
2009, final rule; confirmation of
effective date, the agency also
established a compliance date of
October 26, 2009, in order to allow
additional time for renderers to comply
with the new requirements. The April
24, 2009, final rule; confirmation of
effective date was published with an
inadvertent error in the ‘‘Background’’
section. This document corrects that
error.
DATES: This correction is effective: May
5, 2009.
FOR FURTHER INFORMATION CONTACT:
Joyce A. Strong, Office of Policy,
Planning, and Preparedness (HF–27),
Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857,
301–827–7010.
SUPPLEMENTARY INFORMATION: In FR Doc.
E9–9466, appearing on page 18626 in
the Federal Register of Friday, April 24,
2009, the following correction is made:
On page 18626, in the third column,
under ‘‘I. Background,’’ in the first
paragraph, the first sentence ‘‘In the
Federal Register of April 25, 2008, FDA
published a final rule entitled
‘‘Substances Prohibited From Use in
Animal Food or Feed)’’ (referred to
herein as the April 25, 2008, final rule),
that would become effective 1 year after
the April 27, 2009, date of publication.’’
is corrected to read ‘‘In the Federal
Register of April 25, 2008, FDA
published a final rule entitled
SUMMARY:
BILLING CODE 4160–01–S
21 CFR Part 601
[Docket No. FDA–2009–N–0100]
Revision of the Requirements for
Publication of License Revocation
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Direct final rule.
SUMMARY: The Food and Drug
Administration (FDA) is clarifying the
regulatory procedures for notifying the
public about the revocation of a
biologics license to be consistent with
current practices. FDA is amending the
regulations in accordance with the
agency’s direct final rule procedures.
Elsewhere in this issue of the Federal
Register, we are publishing a
companion proposed rule under FDA’s
usual procedures for notice and
comment rulemaking to provide a
procedural framework to finalize the
rule in the event that we receive any
significant adverse comments on the
direct final rule. If we receive any
significant adverse comments that
warrant terminating the direct final rule,
we will consider such comments on the
proposed rule in developing the final
rule.
DATES: This rule is effective September
17, 2009. Submit written or electronic
comments on or before July 20, 2009. If
FDA receives no significant adverse
comments within the specified
comment period, the agency will
publish a document confirming the
effective date of the final rule in the
Federal Register within 30 days after
the comment period on this direct final
rule ends. If timely significant adverse
comments are received, the agency will
publish a document in the Federal
Register withdrawing this direct final
rule.
ADDRESSES: You may submit comments,
identified by Docket No. FDA–2009–N–
0100, by any of the following methods:
PO 00000
Frm 00025
Fmt 4700
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20583
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Written Submissions
Submit written submissions in the
following ways:
• FAX: 301–827–6870.
• Mail/Hand delivery/Courier [For
paper, disk, or CD–ROM submissions]:
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
To ensure more timely processing of
comments, FDA is no longer accepting
comments submitted to the agency by email. FDA encourages you to continue
to submit electronic comments by using
the Federal eRulemaking Portal, as
described previously, in the ADDRESSES
portion of this document under
Electronic Submissions.
Instructions: All submissions received
must include the agency name and
docket number for this rulemaking. All
comments received may be posted
without change to https://
www.regulations.gov, including any
personal information provided. For
additional information on submitting
comments, see the ‘‘Request for
Comments’’ heading of the
SUPPLEMENTARY INFORMATION section of
this document.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Paul
E. Levine, Jr., Center for Biologics
Evaluation and Research (HFM–17),
Food and Drug Administration, 1401
Rockville Pike, suite 200N, Rockville,
MD 20852–1448, 301–827–6210.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of January 25,
1977 (42 FR 4680), FDA issued a final
rule revising, among other things, the
procedures under part 601 (21 CFR part
601) for issuing, revoking, and
suspending biologics licenses, and
publishing license revocations. FDA
revised these procedures in order to
simplify and codify existing practices,
establish new requirements where
appropriate, and ensure that practices
and procedures would be consistently
applied throughout the agency.
E:\FR\FM\05MYR1.SGM
05MYR1
]]>Agencies
[Federal Register Volume 74, Number 85 (Tuesday, May 5, 2009)]
[Rules and Regulations]
[Page 20583]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-10138]
[[Page 20583]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 589
[Docket No. FDA-2002-N-0031] (formerly Docket No. 2002N-0273)
RIN 0910-AF46
Substances Prohibited From Use in Animal Food or Feed;
Confirmation of Effective Date of Final Rule; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; confirmation of effective date; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is correcting a final
rule; confirmation of effective date, that appeared in the Federal
Register of Friday, April 24, 2009 (74 FR 18626) (the April 24, 2009,
final rule; confirmation of effective date). That document had
confirmed the effective date of April 27, 2009, for a final rule that
published in the Federal Register of April 25, 2008 (73 FR 22720),
entitled ``Substances Prohibited From Use in Animal Food or Feed.'' In
the April 24, 2009, final rule; confirmation of effective date, the
agency also established a compliance date of October 26, 2009, in order
to allow additional time for renderers to comply with the new
requirements. The April 24, 2009, final rule; confirmation of effective
date was published with an inadvertent error in the ``Background''
section. This document corrects that error.
DATES: This correction is effective: May 5, 2009.
FOR FURTHER INFORMATION CONTACT: Joyce A. Strong, Office of Policy,
Planning, and Preparedness (HF-27), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-827-7010.
SUPPLEMENTARY INFORMATION: In FR Doc. E9-9466, appearing on page 18626
in the Federal Register of Friday, April 24, 2009, the following
correction is made:
On page 18626, in the third column, under ``I. Background,'' in the
first paragraph, the first sentence ``In the Federal Register of April
25, 2008, FDA published a final rule entitled ``Substances Prohibited
From Use in Animal Food or Feed)'' (referred to herein as the April 25,
2008, final rule), that would become effective 1 year after the April
27, 2009, date of publication.'' is corrected to read ``In the Federal
Register of April 25, 2008, FDA published a final rule entitled
``Substances Prohibited From Use in Animal Food or Feed'' (referred to
herein as the April 25, 2008, final rule), that would become effective
1 year after that publication.''
Dated: April 28, 2009.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.
[FR Doc. E9-10138 Filed 5-4-09; 8:45 am]
BILLING CODE 4160-01-S
