Defining Small Number of Animals for Minor Use Determination; Periodic Reassessment, 56681-56682 [2022-19955]
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lotter on DSK11XQN23PROD with NOTICES1
Federal Register / Vol. 87, No. 178 / Thursday, September 15, 2022 / Notices
to the drug. However, in 1984, the AntiInfective Drugs Advisory Committee
concluded that intramuscular
administration of bacitracin was not safe
and effective. In addition, in April 2019,
FDA’s Antimicrobial Drugs Advisory
Committee advised that the benefits of
bacitracin for injection do not outweigh
its risks for the drug’s only approved
indication.
Bacitracin for injection poses serious
risks, including nephrotoxicity and
anaphylactic reactions. Healthcare
professionals generally no longer use
bacitracin for injection to treat infants
with pneumonia and empyema because
other effective FDA-approved
treatments are available that do not have
these risks. Out of concern about these
risks, on January 31, 2020, FDA
requested that all application holders of
bacitracin for injection voluntarily
request withdrawal of approval of their
applications under § 314.150(d) (21 CFR
314.150(d)). Two approved applications
for bacitracin for injection had been
withdrawn prior to January 31, 2020
(see 61 FR 40649, August 5, 1996, and
57 FR 6228, February 21, 1992) and
therefore FDA did not need to request
their withdrawal. In a letter dated
February 7, 2020, Pfizer requested
withdrawal of approval of ANDA
060733 (originally NDA 6–483) for
bacitracin for injection under
§ 314.150(d) and waived its opportunity
for a hearing. In separate letters dated
February 5, 2020, Akorn Inc. and Mylan
ASI LLC requested that FDA withdraw
approval of ANDAs 206719 and 090211,
respectively, under § 314.150(d) and
waived their opportunity for a hearing.
Additionally, in separate letters dated
February 7, 2020, X–GEN
Pharmaceuticals, Inc. and Fresenius
Kabi USA, LLC requested that FDA
withdraw approval of ANDAs 064153
and 065116, respectively, under
§ 314.150(d) and waived their
opportunity for a hearing. In the Federal
Register of March 12, 2021 (86 FR
14127), FDA announced that it was
withdrawing approval of ANDAs
060733 (originally NDA 6–483), 206719,
090211, 064153, and 065116, and all
amendments and supplements thereto,
effective March 12, 2021.
In a letter dated June 14, 2021, the
only remaining application holder,
Xellia Pharmaceuticals USA, LLC,
requested that FDA withdraw approval
of ANDA 203177 under § 314.150(d)
and waived its opportunity for a
hearing. In the Federal Register of July
11, 2022 (87 FR 41135), FDA announced
that it was withdrawing approval of
ANDA 203177, and all supplements
thereto, effective July 11, 2022.
Accordingly, the Agency has withdrawn
VerDate Sep<11>2014
16:56 Sep 14, 2022
Jkt 256001
approval of all ANDAs for bacitracin for
injection.
After reviewing Agency records and
based on the information we have at this
time, FDA has determined under
§ 314.161 that bacitracin for injection,
10,000 units/vial and 50,000 units/vial,
was withdrawn for reasons of safety or
effectiveness. We have reviewed our
files for records concerning the
withdrawal of bacitracin for injection
from sale. We have also independently
evaluated relevant literature and data
for possible postmarketing adverse
events. Based on a thorough evaluation
of this information, including
information presented to FDA’s
Antimicrobial Drugs Advisory
Committee and the recommendations of
that committee, and an evaluation of the
latest version of the drug product’s
labeling, we have determined that
bacitracin for injection, 10,000 units/
vial and 50,000 units/vial, would not be
considered safe and effective if it were
introduced to the market today in the
absence of new preclinical or clinical
studies to address safety or effectiveness
concerns identified during our review.
Accordingly, the Agency will remove
bacitracin for injection, 10,000 units/
vial and 50,000 units/vial, from the list
of drug products published in the
Orange Book. FDA will not accept or
approve ANDAs that refer to this drug
product.
Dated: September 9, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022–19995 Filed 9–14–22; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0176]
Defining Small Number of Animals for
Minor Use Determination; Periodic
Reassessment
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA, the Agency, or
we) is announcing the availability of its
most recent periodic reassessment of the
definition of ‘‘small number of animals’’
for minor use in major species
(contained in our existing regulation for
new animal drugs for minor use and
minor species). We also are announcing
that the small number of animals upper
limit thresholds (small numbers) for
SUMMARY:
PO 00000
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Fmt 4703
Sfmt 4703
56681
horses and the food-producing major
species (cattle, pigs, turkeys, and
chickens) will remain the same. We are
separately issuing a direct final rule and
a companion proposed rule to revise
(i.e., increase) the small numbers for
dogs and cats.
DATES: Submit either electronic or
written comments on the notice at any
time.
ADDRESSES: You may submit comments
as follows.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2008–N–0176 for ‘‘Defining Small
Numbers of Animals for Minor Use
Determination; Periodic Reassessment.’’
Received comments will be placed in
the docket and, except for those
submitted as ‘‘Confidential
E:\FR\FM\15SEN1.SGM
15SEN1
56682
Federal Register / Vol. 87, No. 178 / Thursday, September 15, 2022 / Notices
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper 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 Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
FOR FURTHER INFORMATION CONTACT:
Margaret Oeller, Center for Veterinary
Medicine (HVF–50), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240–402–0566,
email: margaret.oeller@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
lotter on DSK11XQN23PROD with NOTICES1
I. Background
The Minor Use and Minor Species
Animal Health Act of 2004 (Pub. L. 108–
282) (the MUMS Act) amended the
Federal Food, Drug, and Cosmetic Act
(FD&C Act) to provide incentives for the
development of new animal drugs for
use in minor animal species and for
VerDate Sep<11>2014
16:56 Sep 14, 2022
Jkt 256001
minor uses in major animal species. The
MUMS Act defines ‘‘minor use’’ as the
intended use of a drug in a major
species for an indication that occurs
infrequently and in only a small number
of animals or in limited geographical
areas and in only a small number of
animals annually (see section 201(pp) of
the FD&C Act (21 U.S.C. 321(pp)).
In the Federal Register of August 26,
2009 (74 FR 43043), we issued a final
rule to define the term ‘‘small number
of animals’’ by establishing for each
major species of animal (horses, dogs,
cats, cattle, pigs, turkeys, and chickens)
an upper limit threshold (i.e., small
number) to provide a means of
determining whether any particular
intended use of a new animal drug in
one of these species would qualify as a
minor use under the MUMS Act. The
small numbers for the seven major
species of animals as established in the
‘‘small number of animals’’ definition at
21 CFR 516.3(b) are 50,000 horses,
70,000 dogs, 120,000 cats, 310,000
cattle, 1,450,000 pigs, 14,000,000
turkeys, and 72,000,000 chickens.
In our final rule, in response to
comments, we agreed that periodic
reassessment of the small numbers is
appropriate and that such reassessments
should occur approximately every 5
years. We conducted our first
reassessment in 2013 and published the
results in the Federal Register on May
19, 2014 (79 FR 28736). We concluded,
based on that reassessment, that no
changes to the definition of ‘‘small
number of animals’’ were needed.
II. Current Reassessment
We conducted our second
reassessment of the ‘‘small number of
animals’’ definition in 2018–2019
(current reassessment), and the results
of that reassessment are summarized in
our memorandum ‘‘2018–2019
Reassessment of Small Numbers of
Animals for Minor Use Determination’’
(Ref. 1). FDA developed different
processes for establishing small
numbers for the major species of
companion animals and the major
species of food-producing animals, and
we continue to use those processes for
our periodic reassessments of the small
numbers. Both processes are described
in detail in the preamble to the
proposed rule that published in the
Federal Register on March 18, 2008 (73
FR 14411) and in our memorandum for
the current reassessment (Ref. 1).
Based on our current reassessment,
there is not an adequate basis to propose
revisions to the currently published
small numbers for horses and the foodproducing major species. The small
numbers for horses and the four food-
PO 00000
Frm 00063
Fmt 4703
Sfmt 9990
producing major species as established
in the current ‘‘small number of
animals’’ definition in § 516.3(b) are
listed in table 1.
TABLE 1—CURRENT SMALL NUMBERS
FOR HORSES AND THE FOOD-PRODUCING MAJOR SPECIES
[21 CFR 516.3(b)]
Species
Horses ......................................
Cattle ........................................
Pigs ...........................................
Turkeys .....................................
Chickens ...................................
Small No.
50,000
310,000
1,450,000
14,000,000
72,000,000
In separate documents published
elsewhere in this issue of the Federal
Register, we are publishing a direct final
rule to revise (i.e., increase) the ‘‘small
numbers’’ for dogs and cats, and a
proposed rule as a companion to the
direct final rule under FDA’s usual
procedures for notice and comment.
III. Paperwork Reduction Act of 1995
While this notice of reassessment of
the small numbers contains no
collection of information, it does refer to
previously approved FDA collections of
information. Therefore, clearance by the
Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995 (PRA) (44 U.S.C. 3501–
3521) is not required for this notice. The
previously approved collections of
information are subject to review by
OMB under the PRA. The collections of
information in 21 CFR 516.20 have been
approved under OMB control number
0910–0605.
IV. References
The following reference is on display
at the Dockets Management Staff (see
ADDRESSES) and is available for viewing
by interested persons between 9 a.m.
and 4 p.m., Monday through Friday; it
is also available electronically at https://
www.regulations.gov.
1. FDA Memorandum, ‘‘2018–2019
Reassessment of Small Numbers of
Animals for Minor Use Determination,’’
2021.
Dated: September 9, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022–19955 Filed 9–14–22; 8:45 am]
BILLING CODE 4164–01–P
E:\FR\FM\15SEN1.SGM
15SEN1
Agencies
[Federal Register Volume 87, Number 178 (Thursday, September 15, 2022)]
[Notices]
[Pages 56681-56682]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-19955]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2008-N-0176]
Defining Small Number of Animals for Minor Use Determination;
Periodic Reassessment
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA, the Agency, or we) is
announcing the availability of its most recent periodic reassessment of
the definition of ``small number of animals'' for minor use in major
species (contained in our existing regulation for new animal drugs for
minor use and minor species). We also are announcing that the small
number of animals upper limit thresholds (small numbers) for horses and
the food-producing major species (cattle, pigs, turkeys, and chickens)
will remain the same. We are separately issuing a direct final rule and
a companion proposed rule to revise (i.e., increase) the small numbers
for dogs and cats.
DATES: Submit either electronic or written comments on the notice at
any time.
ADDRESSES: You may submit comments as follows.
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to https://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2008-N-0176 for ``Defining Small Numbers of Animals for Minor Use
Determination; Periodic Reassessment.'' Received comments will be
placed in the docket and, except for those submitted as ``Confidential
[[Page 56682]]
Submissions,'' publicly viewable at https://www.regulations.gov or at
the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through
Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will
review this copy, including the claimed confidential information, in
its consideration of comments. The second copy, which will have the
claimed confidential information redacted/blacked out, will be
available for public viewing and posted on https://www.regulations.gov.
Submit both copies to the Dockets Management Staff. If you do not wish
your name and contact information to be made publicly available, you
can provide this information on the cover sheet and not in the body of
your comments and you must identify this information as
``confidential.'' Any information marked as ``confidential'' will not
be disclosed except in accordance with 21 CFR 10.20 and other
applicable disclosure law. For more information about FDA's posting of
comments to public dockets, see 80 FR 56469, September 18, 2015, or
access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper 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 Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
FOR FURTHER INFORMATION CONTACT: Margaret Oeller, Center for Veterinary
Medicine (HVF-50), Food and Drug Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240-402-0566, email: [email protected].
SUPPLEMENTARY INFORMATION:
I. Background
The Minor Use and Minor Species Animal Health Act of 2004 (Pub. L.
108-282) (the MUMS Act) amended the Federal Food, Drug, and Cosmetic
Act (FD&C Act) to provide incentives for the development of new animal
drugs for use in minor animal species and for minor uses in major
animal species. The MUMS Act defines ``minor use'' as the intended use
of a drug in a major species for an indication that occurs infrequently
and in only a small number of animals or in limited geographical areas
and in only a small number of animals annually (see section 201(pp) of
the FD&C Act (21 U.S.C. 321(pp)).
In the Federal Register of August 26, 2009 (74 FR 43043), we issued
a final rule to define the term ``small number of animals'' by
establishing for each major species of animal (horses, dogs, cats,
cattle, pigs, turkeys, and chickens) an upper limit threshold (i.e.,
small number) to provide a means of determining whether any particular
intended use of a new animal drug in one of these species would qualify
as a minor use under the MUMS Act. The small numbers for the seven
major species of animals as established in the ``small number of
animals'' definition at 21 CFR 516.3(b) are 50,000 horses, 70,000 dogs,
120,000 cats, 310,000 cattle, 1,450,000 pigs, 14,000,000 turkeys, and
72,000,000 chickens.
In our final rule, in response to comments, we agreed that periodic
reassessment of the small numbers is appropriate and that such
reassessments should occur approximately every 5 years. We conducted
our first reassessment in 2013 and published the results in the Federal
Register on May 19, 2014 (79 FR 28736). We concluded, based on that
reassessment, that no changes to the definition of ``small number of
animals'' were needed.
II. Current Reassessment
We conducted our second reassessment of the ``small number of
animals'' definition in 2018-2019 (current reassessment), and the
results of that reassessment are summarized in our memorandum ``2018-
2019 Reassessment of Small Numbers of Animals for Minor Use
Determination'' (Ref. 1). FDA developed different processes for
establishing small numbers for the major species of companion animals
and the major species of food-producing animals, and we continue to use
those processes for our periodic reassessments of the small numbers.
Both processes are described in detail in the preamble to the proposed
rule that published in the Federal Register on March 18, 2008 (73 FR
14411) and in our memorandum for the current reassessment (Ref. 1).
Based on our current reassessment, there is not an adequate basis
to propose revisions to the currently published small numbers for
horses and the food-producing major species. The small numbers for
horses and the four food-producing major species as established in the
current ``small number of animals'' definition in Sec. 516.3(b) are
listed in table 1.
Table 1--Current Small Numbers for Horses and the Food-Producing Major
Species
[21 CFR 516.3(b)]
------------------------------------------------------------------------
Species Small No.
------------------------------------------------------------------------
Horses..................................................... 50,000
Cattle..................................................... 310,000
Pigs....................................................... 1,450,000
Turkeys.................................................... 14,000,000
Chickens................................................... 72,000,000
------------------------------------------------------------------------
In separate documents published elsewhere in this issue of the
Federal Register, we are publishing a direct final rule to revise
(i.e., increase) the ``small numbers'' for dogs and cats, and a
proposed rule as a companion to the direct final rule under FDA's usual
procedures for notice and comment.
III. Paperwork Reduction Act of 1995
While this notice of reassessment of the small numbers contains no
collection of information, it does refer to previously approved FDA
collections of information. Therefore, clearance by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3521) is not required for this notice. The
previously approved collections of information are subject to review by
OMB under the PRA. The collections of information in 21 CFR 516.20 have
been approved under OMB control number 0910-0605.
IV. References
The following reference is on display at the Dockets Management
Staff (see ADDRESSES) and is available for viewing by interested
persons between 9 a.m. and 4 p.m., Monday through Friday; it is also
available electronically at https://www.regulations.gov.
1. FDA Memorandum, ``2018-2019 Reassessment of Small Numbers of
Animals for Minor Use Determination,'' 2021.
Dated: September 9, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022-19955 Filed 9-14-22; 8:45 am]
BILLING CODE 4164-01-P