New Animal Drugs; Change of Sponsor, 21058-21060 [2013-07542]
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21058
Federal Register / Vol. 78, No. 68 / Tuesday, April 9, 2013 / Rules and Regulations
Note. The Commission has the power
under Section 19(b)(3)(C) of the Act
summarily to temporarily suspend within
sixty days of its filing any proposed rule
change which has taken effect upon filing
pursuant to Section 19(b)(3)(A) of the Act or
was put into effect summarily by the
Commission pursuant to Section 19(b)(3)(B)
of the Act. In exercising its summary power
under Section 19(b)(3)(B), the Commission is
required to make one of the findings
described above but may not have a full
opportunity to make a determination that the
proposed rule change otherwise is consistent
with the requirements of the Act and the
rules and regulations thereunder. The
Commission will generally exercise its
summary power under Section 19(b)(3)(B) on
condition that the proposed rule change to be
declared effective summarily shall also be
subject to the filing procedures of Section
19(b)(1) of the Act, for approval pursuant to
Section 19(b)(2). Accordingly, in most cases,
a summary order under Section 19(b)(3)(B)
shall be effective until such time as the
Commission enters an order, pursuant to
Section 19(b)(2)(A) of the Exchange Act, to
approve such proposed rule change or,
depending on the circumstances, until such
time as the Commission summarily
temporarily suspends the rule change
pursuant to Section 19(b)(3)(C) or,
alternatively, until such time as the
Commission, at the conclusion of
proceedings to determine whether to approve
or disapprove the proposed rule change,
enters an order, pursuant to Section
19(b)(2)(B), approving or disapproving such
proposed rule change. Similarly, the
Commission requires that any proposed rule
change which has taken effect upon filing
pursuant to paragraph (B)(II) of Rule 19b–
4(f)(4)(ii) shall also be subject to the filing
procedures of Section 19(b)(1) of the Act, for
approval pursuant to Section 19(b)(2) of the
Act. Accordingly, such rule change shall be
effective until such time as the Commission
enters an order, pursuant to Section
19(b)(2)(A) of the Exchange Act, to approve
such proposed rule change or, depending on
the circumstances, until such time as the
Commission summarily temporarily
suspends the rule change pursuant to Section
19(b)(3)(C) or, alternatively, until such time
as the Commission, at the conclusion of
proceedings to determine whether to approve
or disapprove the proposed rule change,
enters an order, pursuant to Section
19(b)(2)(B), approving or disapproving such
proposed rule change.
By the Commission.
Dated: April 3, 2013.
Elizabeth M. Murphy,
Secretary.
[FR Doc. 2013–08141 Filed 4–8–13; 8:45 am]
BILLING CODE 8011–01–P
ACTION:
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
animal drug regulations to reflect a
change of sponsor for 43 approved new
animal drug applications (NADAs) and
3 approved abbreviated new animal
drug applications (ANADAs) from
Boehringer Ingelheim Vetmedica, Inc. to
Strategic Veterinary Pharmaceuticals,
Inc.
DATES:
This rule is effective April 9,
2013.
FOR FURTHER INFORMATION CONTACT:
Steven D. Vaughn, Center for Veterinary
Medicine (HFV–100), Food and Drug
Administration, 7520 Standish Pl.,
Rockville, MD 20855, 240–276–8300,
email: steven.vaughn@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 510, 520, 522, 524, 526,
529, and 558
[Docket No. FDA–2013–N–0002]
Boehringer Ingelheim Vetmedica, Inc.,
2621 North Belt Highway, St. Joseph,
MO 64506–2002 has informed FDA that
it has transferred ownership of, and all
rights and interest in, the following 43
approved NADAs and 3 approved
ANADAs to Strategic Veterinary
Pharmaceuticals, Inc., 100 NW. Airport
Rd., St. Joseph, MO 64503:
New Animal Drugs; Change of Sponsor
AGENCY:
Food and Drug Administration,
HHS.
TABLE 1.—APPLICATIONS TRANSFERRED
tkelley on DSK3SPTVN1PROD with RULES
Application No.
11–531 .......................
11–674 .......................
12–469 .......................
31–512 .......................
33–803 .......................
35–918 .......................
38–200 .......................
39–483 .......................
40–848 .......................
43–606 .......................
45–143 .......................
47–278 .......................
47–712 .......................
48–010 .......................
48–237 .......................
48–271 .......................
49–032 .......................
55–097 .......................
65–178 .......................
65–461 .......................
65–481 .......................
65–486 .......................
65–491 .......................
65–496 .......................
92–837 .......................
93–516 .......................
97–452 .......................
98–569 .......................
99–618 .......................
108–963 .....................
VerDate Mar<15>2010
Trade name
DIZAN (dithiazanine iodide) Tablets.
DIZAN (dithiazanine iodide) Powder.
DIZAN Suspension With Piperazine.
ATGARD (dichlovos) Swine Wormer Type A Medicated Article.
TASK (dichlovos) Dog Anthelmintic.
EQUIGARD (dichlovos).
MEDAMYCIN (oxytetracycline hydrochloride) Soluble Antibiotic.
BIO-TAL (thiamylal sodium) Injectable Solution.
ATGARD C (dichlovos) Swine Wormer Type A Medicated Article.
ATGARD V (dichlovos) Swine Wormer Type A Medicated Article.
OXYJECT (oxytetracycline hydrochloride) Injectable Solution.
OXY-TET 50 (oxytetracycline hydrochloride) Injectable Solution.
BIZOLIN-100 (phenylbutazone) Tablets.
ANAPLEX (dichlorophene and toluene) Capsules.
EQUIGEL (dichlovos) Oral Gel.
TASK (dichlovos) Tablets.
ATGARD C (dichlovos) 9.6% Type A Medicated Article.
DRY-MAST (penicillin G procaine/dihydrostreptomycin sulfate) Intramammary Infusion.
FERMYCIN (chlortetracycline hydrochloride or chlortetracycline bisulfate) Soluble Powder.
ANACETIN (chloramphenicol) Tablets.
Chlortetracycline Pneumonia/Calf Scour Boluses.
Chlortetracycline Bisulfate Soluble Powder.
MEDICHOL (chloramphenicol) Tablets.
Tetracycline Soluble Powder.
NEMACIDE (diethylcarbamazine citrate) Oral Syrup.
BIZOLIN (phenylbutazone) Injection 20%.
OXYJECT 100 (oxytetracycline hydrochloride) Injectable Solution.
MEDACIDE-SDM (sulfadimethoxine) Injection 10%.
BIZOLIN (phenylbutazone) 1–G Tablets.
MEDAMYCIN (oxytetracycline hydrochloride) Injectable Solution.
16:04 Apr 08, 2013
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Federal Register / Vol. 78, No. 68 / Tuesday, April 9, 2013 / Rules and Regulations
21059
TABLE 1.—APPLICATIONS TRANSFERRED—Continued
Application No.
109–305
117–689
125–797
126–236
126–676
127–627
128–069
132–028
135–771
136–212
137–310
138–869
140–442
200–023
200–029
200–165
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
Trade name
Oxytocin Injection.
NEUROSYN (primidone) Tablets.
Nitrofurazone Dressing.
Nitrofurazone Soluble Powder.
D & T (dichlorophene and toluene) Worm Capsules.
NEMACIDE-C (diethylcarbamazine citrate) Tablets.
NEMACIDE (diethylcarbamazine citrate) Chewable Tablets.
ANESTATAL (thiamylal sodium) Powder for Injection.
Methylprednisolene Tablets.
Methylprednisolone Acetate Injectable Suspension.
Gentamicin Sulfate Injectable Solution.
Triamcinolone Acetonide Injectable Suspension.
Xylazine HCl Injection.
Gentamicin Sulfate Intrauterine Solution.
Ketamine Hydrochloride Injection.
SDM (sulfadimethoxine) 12.5% Oral Solution.
Accordingly, the Agency is amending
the regulations in 21 CFR parts 510, 520,
522, 524, 526, 529, and 558 to reflect the
transfer of ownership.
This rule does not meet the definition
of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because
it is a rule of ‘‘particular applicability.’’
Therefore, it is not subject to the
congressional review requirements in 5
U.S.C. 801–808.
§ 510.600 Names, addresses, and drug
labeler codes of sponsors of approved
applications.
List of Subjects
*
*
*
Strategic Veterinary Pharmaceuticals, Inc., 100 NW.
Airport Rd., St. Joseph,
MO 64503 .........................
21 CFR Part 510
Administrative practice and
procedure, Animal drugs, Labeling,
Reporting and recordkeeping
requirements.
*
*
*
(c) * * *
(1) * * *
*
§ 520.443
6. In paragraph (b) of § 520.443,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
*
§ 520.580
Drug labeler
code
Firm name and address
*
*
*
*
054628
*
*
Drug labeler
code
Firm name and address
21 CFR Part 558
Animal drugs, Animal feeds.
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs and redelegated to
the Center for Veterinary Medicine, 21
CFR parts 510, 520, 522, 524, 526, 529,
and 558 are amended as follows:
*
*
*
*
*
054628 ........ Strategic Veterinary Pharmaceuticals, Inc., 100 NW. Airport Rd., St. Joseph, MO
64503
*
*
[Amended]
8. In paragraph (c) of § 520.600,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
[Amended]
9. In paragraph (a)(6) of § 520.622a,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
§ 520.622b
[Amended]
10. In paragraph (c)(2) of § 520.622b,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
§ 520.390a
11. In paragraph (b)(6) of § 520.622c,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
[Amended]
Frm 00045
Fmt 4700
12. In § 520.763a, remove and reserve
paragraph (a); in paragraph (c), remove
‘‘000010’’ and in its place add
‘‘054628’’; and remove paragraph (e).
■
[Amended]
13. In § 520.763b, remove and reserve
paragraph (a); and in paragraph (c),
remove ‘‘000010’’ and in its place add
‘‘054628’’.
§ 520.763c
[Amended]
14. In paragraph (b) of § 520.763c,
remove ‘‘000010’’ and in its place add
‘‘054628’’; and remove and reserve
paragraph (c).
■
5. In paragraph (b)(3) of § 520.441,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
PO 00000
[Amended]
■
[Amended]
4. In paragraph (b)(1)(i) of § 520.390a,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
§ 520.441
[Amended]
■
§ 520.763b
■
2. In the table in paragraph (c)(1) of
§ 510.600, alphabetically add an entry
for ‘‘Strategic Veterinary
Pharmaceuticals, Inc.’’; and in the table
in paragraph (c)(2), numerically add an
entry for ‘‘054628’’ to read as follows:
§ 520.622c
§ 520.763a
Authority: 21 U.S.C. 360b.
Authority: 21 U.S.C. 321, 331, 351, 352,
353, 360b, 371, 379e.
tkelley on DSK3SPTVN1PROD with RULES
*
3. The authority citation for 21 CFR
part 520 continues to read as follows:
1. The authority citation for 21 CFR
part 510 continues to read as follows:
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*
PART 520—ORAL DOSAGE FORM
NEW ANIMAL DRUGS
■
■
*
■
PART 510—NEW ANIMAL DRUGS
16:04 Apr 08, 2013
§ 520.600
■
Animal drugs.
VerDate Mar<15>2010
7. In paragraph (b)(2), remove
‘‘000010 and 000061’’ and in its place
add ‘‘Nos. 000061 and 054628’’.
■
(2) * * *
21 CFR Parts 520, 522, 524, 526, and
529
[Amended]
■
§ 520.622a
*
[Amended]
Sfmt 4700
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09APR1
21060
§ 520.1408
Federal Register / Vol. 78, No. 68 / Tuesday, April 9, 2013 / Rules and Regulations
[Amended]
§ 522.1662a
15. In paragraph (b) of § 520.1408,
remove ‘‘000010’’ and in its place add
‘‘054628’’; and remove and reserve
paragraph (c).
■
§ 520.1660d
[Amended]
16. In § 520.1660d:
a. In paragraph (b)(3), remove
‘‘000010’’ and in its place add
‘‘054628’’.
■ b. In paragraph (d)(1)(ii)(A)(3), remove
‘‘000010’’ and in its place add
‘‘054628’’.
■ c. In paragraph (d)(1)(ii)(B)(3), remove
‘‘000010’’ and in its place add
‘‘054628’’.
■ d. In paragraph (d)(1)(ii)(C)(3), remove
‘‘000010’’ and in its place add
‘‘054628’’.
■
■
§ 520.1720a
17. In paragraph (b)(2) of § 520.1720a,
remove ‘‘000010 and 000859’’ and in its
place add ‘‘000859 and 054628’’.
[Amended]
[Amended]
19. In paragraph (a)(1) of § 520.2220a,
remove ‘‘000010, 000069, 000859,
054925, and 057561’’ and in its place
add ‘‘000069, 000859, 054628, 054925,
and 057561’’.
■
§ 520.2345d
§ 522.1680
Oxytocin.
*
*
*
*
*
27. In § 522.1720, revise the section
heading to read as set forth below; and
in paragraph (b)(2), remove ‘‘000010’’
and in its place add ‘‘054628’’.
■
§ 522.1720
*
*
*
*
28. In § 522.2220, revise the section
heading as set forth below; and in
paragraph (c)(2), remove ‘‘000010’’ and
in its place add ‘‘054628’’.
■
Sulfadimethoxine.
*
*
*
*
*
■ 29. In § 522.2424, revise the section
heading as set forth below; and in
paragraph (b), remove ‘‘000010 and
000856’’ and in its place add ‘‘000856
and 054628’’; and remove paragraph
(c)(4).
§ 522.2424
*
*
§ 522.2483
[Amended]
20. In paragraph (b)(2) of § 520.2345d,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
*
[Amended]
30. In paragraph (b) of § 522.2483,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
[Amended]
[Amended]
36. In paragraph (b) of § 526.1696b,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
PART 529—CERTAIN OTHER DOSAGE
FORM NEW ANIMAL DRUGS
37. The authority citation for 21 CFR
part 529 continues to read as follows:
■
Authority: 21 U.S.C. 360b.
[Amended]
38. In paragraph (b) of § 529.1044a,
remove ‘‘000010, 000061, 000856,
000859 057561, 058005, and 061623’’
and in its place add ‘‘000061, 000856,
000859, 054628, 057561, 058005, and
061623’’.
■
PART 558—NEW ANIMAL DRUGS FOR
USE IN ANIMAL FEEDS
39. The authority citation for 21 CFR
part 558 continues to read as follows:
■
Authority: 21 U.S.C. 360b, 371.
§ 558.205
[Amended]
Dated: March 26, 2013.
Steven D. Vaughn,
Director, Office of New Animal Drug
Evaluation, Center for Veterinary Medicine.
[FR Doc. 2013–07542 Filed 4–8–13; 8:45 am]
31. In paragraph (b)(1) of § 522.2662,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
21. The authority citation for 21 CFR
part 522 continues to read as follows:
Authority: 21 U.S.C. 360b.
PART 524—OPHTHALMIC AND
TOPICAL DOSAGE FORM NEW
ANIMAL DRUGS
[Amended]
32. The authority citation for 21 CFR
part 524 continues to read as follows:
22. In paragraph (b)(3) of § 522.1044,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
§ 522.1222a
§ 524.1580b
DEPARTMENT OF THE INTERIOR
National Indian Gaming Commission
25 CFR Parts 581, 584, and 585
RIN 3141–AA47
■
■
[Amended]
Authority: 21 U.S.C. 360b.
■
§ 522.1410
§ 524.1580c
[Amended]
24. In paragraph (b) of § 522.1410,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
VerDate Mar<15>2010
16:04 Apr 08, 2013
Jkt 229001
[Amended]
34. In paragraph (b) of § 524.1580c,
remove ‘‘000010 and 000069’’ and in its
place add ‘‘000069 and 054628’’.
■
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Appeal Proceedings Before the
Commission
National Indian Gaming
Commission, Interior.
ACTION: Final rule.
AGENCY:
[Amended]
33. In paragraph (b)(1) of § 524.1580b,
remove ‘‘000010, 000069, 050749,
054925, 058005, and 061623’’ and in its
place add ‘‘000069, 050749, 054628,
054925, 058005, and 061623’’.
23. In paragraph (b) of § 522.1222a,
remove ‘‘000010, 000859, 061690,
026637, and 063286’’ and in its place
add ‘‘000859, 026637, 054628, 061690,
and 063286’’.
■
tkelley on DSK3SPTVN1PROD with RULES
§ 526.1696b
BILLING CODE 4160–01–P
■
§ 522.1044
Authority: 21 U.S.C. 360b.
40. In paragraph (a) of § 558.205,
remove ‘‘000010’’ and in its place add
‘‘054628’’.
■
§ 522.2662
PART 522—IMPLANTATION OR
INJECTABLE DOSAGE FORM NEW
ANIMAL DRUGS
*
35. The authority citation for 21 CFR
part 526 continues to read as follows:
■
■
Sodium thiamylal.
*
PART 526—INTRAMAMMARY DOSAGE
FORM NEW ANIMAL DRUGS
§ 529.1044a
Phenylbutazone.
§ 522.2220
18. In paragraph (b) of § 520.1900,
remove ‘‘000010’’ and in its place add
‘‘054628’’; and in paragraphs (c)(1),
(c)(2), and (c)(3), remove the footnote.
■
§ 520.2220a
25. In paragraphs (a)(2), (b)(2), (g)(2),
and (h)(2) of § 522.1662a, remove
‘‘000010’’ and in its place add
‘‘054628’’.
■ 26. In § 522.1680, revise the section
heading to read as set forth below; and
in paragraph (b), remove ‘‘000010,
000856, 000859, and 061623’’ and in its
place add ‘‘000856, 000859, 054628, and
061623’’.
■
*
[Amended]
■
§ 520.1900
[Amended]
SUMMARY: The National Indian Gaming
Commission (NIGC or Commission) is
revising its appeals regulations to
include, amongst the appealable actions,
the Chair’s decisions to approve or
object to a tribal gaming regulatory
authority’s adoption of alternate
standards from those required by the
E:\FR\FM\09APR1.SGM
09APR1
Agencies
[Federal Register Volume 78, Number 68 (Tuesday, April 9, 2013)]
[Rules and Regulations]
[Pages 21058-21060]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-07542]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 510, 520, 522, 524, 526, 529, and 558
[Docket No. FDA-2013-N-0002]
New Animal Drugs; Change of Sponsor
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is amending the animal
drug regulations to reflect a change of sponsor for 43 approved new
animal drug applications (NADAs) and 3 approved abbreviated new animal
drug applications (ANADAs) from Boehringer Ingelheim Vetmedica, Inc. to
Strategic Veterinary Pharmaceuticals, Inc.
DATES: This rule is effective April 9, 2013.
FOR FURTHER INFORMATION CONTACT: Steven D. Vaughn, Center for
Veterinary Medicine (HFV-100), Food and Drug Administration, 7520
Standish Pl., Rockville, MD 20855, 240-276-8300, email:
steven.vaughn@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Boehringer Ingelheim Vetmedica, Inc., 2621
North Belt Highway, St. Joseph, MO 64506-2002 has informed FDA that it
has transferred ownership of, and all rights and interest in, the
following 43 approved NADAs and 3 approved ANADAs to Strategic
Veterinary Pharmaceuticals, Inc., 100 NW. Airport Rd., St. Joseph, MO
64503:
Table 1.--Applications Transferred
------------------------------------------------------------------------
Application No. Trade name
------------------------------------------------------------------------
11-531........................... DIZAN (dithiazanine iodide) Tablets.
11-674........................... DIZAN (dithiazanine iodide) Powder.
12-469........................... DIZAN Suspension With Piperazine.
31-512........................... ATGARD (dichlovos) Swine Wormer Type
A Medicated Article.
33-803........................... TASK (dichlovos) Dog Anthelmintic.
35-918........................... EQUIGARD (dichlovos).
38-200........................... MEDAMYCIN (oxytetracycline
hydrochloride) Soluble Antibiotic.
39-483........................... BIO-TAL (thiamylal sodium) Injectable
Solution.
40-848........................... ATGARD C (dichlovos) Swine Wormer
Type A Medicated Article.
43-606........................... ATGARD V (dichlovos) Swine Wormer
Type A Medicated Article.
45-143........................... OXYJECT (oxytetracycline
hydrochloride) Injectable Solution.
47-278........................... OXY-TET 50 (oxytetracycline
hydrochloride) Injectable Solution.
47-712........................... BIZOLIN-100 (phenylbutazone) Tablets.
48-010........................... ANAPLEX (dichlorophene and toluene)
Capsules.
48-237........................... EQUIGEL (dichlovos) Oral Gel.
48-271........................... TASK (dichlovos) Tablets.
49-032........................... ATGARD C (dichlovos) 9.6% Type A
Medicated Article.
55-097........................... DRY-MAST (penicillin G procaine/
dihydrostreptomycin sulfate)
Intramammary Infusion.
65-178........................... FERMYCIN (chlortetracycline
hydrochloride or chlortetracycline
bisulfate) Soluble Powder.
65-461........................... ANACETIN (chloramphenicol) Tablets.
65-481........................... Chlortetracycline Pneumonia/Calf
Scour Boluses.
65-486........................... Chlortetracycline Bisulfate Soluble
Powder.
65-491........................... MEDICHOL (chloramphenicol) Tablets.
65-496........................... Tetracycline Soluble Powder.
92-837........................... NEMACIDE (diethylcarbamazine citrate)
Oral Syrup.
93-516........................... BIZOLIN (phenylbutazone) Injection
20%.
97-452........................... OXYJECT 100 (oxytetracycline
hydrochloride) Injectable Solution.
98-569........................... MEDACIDE-SDM (sulfadimethoxine)
Injection 10%.
99-618........................... BIZOLIN (phenylbutazone) 1-G Tablets.
108-963.......................... MEDAMYCIN (oxytetracycline
hydrochloride) Injectable Solution.
[[Page 21059]]
109-305.......................... Oxytocin Injection.
117-689.......................... NEUROSYN (primidone) Tablets.
125-797.......................... Nitrofurazone Dressing.
126-236.......................... Nitrofurazone Soluble Powder.
126-676.......................... D & T (dichlorophene and toluene)
Worm Capsules.
127-627.......................... NEMACIDE-C (diethylcarbamazine
citrate) Tablets.
128-069.......................... NEMACIDE (diethylcarbamazine citrate)
Chewable Tablets.
132-028.......................... ANESTATAL (thiamylal sodium) Powder
for Injection.
135-771.......................... Methylprednisolene Tablets.
136-212.......................... Methylprednisolone Acetate Injectable
Suspension.
137-310.......................... Gentamicin Sulfate Injectable
Solution.
138-869.......................... Triamcinolone Acetonide Injectable
Suspension.
140-442.......................... Xylazine HCl Injection.
200-023.......................... Gentamicin Sulfate Intrauterine
Solution.
200-029.......................... Ketamine Hydrochloride Injection.
200-165.......................... SDM (sulfadimethoxine) 12.5% Oral
Solution.
------------------------------------------------------------------------
Accordingly, the Agency is amending the regulations in 21 CFR parts
510, 520, 522, 524, 526, 529, and 558 to reflect the transfer of
ownership.
This rule does not meet the definition of ``rule'' in 5 U.S.C.
804(3)(A) because it is a rule of ``particular applicability.''
Therefore, it is not subject to the congressional review requirements
in 5 U.S.C. 801-808.
List of Subjects
21 CFR Part 510
Administrative practice and procedure, Animal drugs, Labeling,
Reporting and recordkeeping requirements.
21 CFR Parts 520, 522, 524, 526, and 529
Animal drugs.
21 CFR Part 558
Animal drugs, Animal feeds.
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs and
redelegated to the Center for Veterinary Medicine, 21 CFR parts 510,
520, 522, 524, 526, 529, and 558 are amended as follows:
PART 510--NEW ANIMAL DRUGS
0
1. The authority citation for 21 CFR part 510 continues to read as
follows:
Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e.
0
2. In the table in paragraph (c)(1) of Sec. 510.600, alphabetically
add an entry for ``Strategic Veterinary Pharmaceuticals, Inc.''; and in
the table in paragraph (c)(2), numerically add an entry for ``054628''
to read as follows:
Sec. 510.600 Names, addresses, and drug labeler codes of sponsors of
approved applications.
* * * * *
(c) * * *
(1) * * *
------------------------------------------------------------------------
Drug labeler
Firm name and address code
------------------------------------------------------------------------
* * * * *
Strategic Veterinary Pharmaceuticals, Inc., 100 NW. 054628
Airport Rd., St. Joseph, MO 64503......................
* * * * *
------------------------------------------------------------------------
(2) * * *
------------------------------------------------------------------------
Drug labeler code Firm name and address
------------------------------------------------------------------------
* * * * *
054628.............................. Strategic Veterinary
Pharmaceuticals, Inc., 100 NW.
Airport Rd., St. Joseph, MO 64503
* * * * *
------------------------------------------------------------------------
PART 520--ORAL DOSAGE FORM NEW ANIMAL DRUGS
0
3. The authority citation for 21 CFR part 520 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 520.390a [Amended]
0
4. In paragraph (b)(1)(i) of Sec. 520.390a, remove ``000010'' and in
its place add ``054628''.
Sec. 520.441 [Amended]
0
5. In paragraph (b)(3) of Sec. 520.441, remove ``000010'' and in its
place add ``054628''.
Sec. 520.443 [Amended]
0
6. In paragraph (b) of Sec. 520.443, remove ``000010'' and in its
place add ``054628''.
Sec. 520.580 [Amended]
0
7. In paragraph (b)(2), remove ``000010 and 000061'' and in its place
add ``Nos. 000061 and 054628''.
Sec. 520.600 [Amended]
0
8. In paragraph (c) of Sec. 520.600, remove ``000010'' and in its
place add ``054628''.
Sec. 520.622a [Amended]
0
9. In paragraph (a)(6) of Sec. 520.622a, remove ``000010'' and in its
place add ``054628''.
Sec. 520.622b [Amended]
0
10. In paragraph (c)(2) of Sec. 520.622b, remove ``000010'' and in its
place add ``054628''.
Sec. 520.622c [Amended]
0
11. In paragraph (b)(6) of Sec. 520.622c, remove ``000010'' and in its
place add ``054628''.
Sec. 520.763a [Amended]
0
12. In Sec. 520.763a, remove and reserve paragraph (a); in paragraph
(c), remove ``000010'' and in its place add ``054628''; and remove
paragraph (e).
Sec. 520.763b [Amended]
0
13. In Sec. 520.763b, remove and reserve paragraph (a); and in
paragraph (c), remove ``000010'' and in its place add ``054628''.
Sec. 520.763c [Amended]
0
14. In paragraph (b) of Sec. 520.763c, remove ``000010'' and in its
place add ``054628''; and remove and reserve paragraph (c).
[[Page 21060]]
Sec. 520.1408 [Amended]
0
15. In paragraph (b) of Sec. 520.1408, remove ``000010'' and in its
place add ``054628''; and remove and reserve paragraph (c).
Sec. 520.1660d [Amended]
0
16. In Sec. 520.1660d:
0
a. In paragraph (b)(3), remove ``000010'' and in its place add
``054628''.
0
b. In paragraph (d)(1)(ii)(A)(3), remove ``000010'' and in its place
add ``054628''.
0
c. In paragraph (d)(1)(ii)(B)(3), remove ``000010'' and in its place
add ``054628''.
0
d. In paragraph (d)(1)(ii)(C)(3), remove ``000010'' and in its place
add ``054628''.
Sec. 520.1720a [Amended]
0
17. In paragraph (b)(2) of Sec. 520.1720a, remove ``000010 and
000859'' and in its place add ``000859 and 054628''.
Sec. 520.1900 [Amended]
0
18. In paragraph (b) of Sec. 520.1900, remove ``000010'' and in its
place add ``054628''; and in paragraphs (c)(1), (c)(2), and (c)(3),
remove the footnote.
Sec. 520.2220a [Amended]
0
19. In paragraph (a)(1) of Sec. 520.2220a, remove ``000010, 000069,
000859, 054925, and 057561'' and in its place add ``000069, 000859,
054628, 054925, and 057561''.
Sec. 520.2345d [Amended]
0
20. In paragraph (b)(2) of Sec. 520.2345d, remove ``000010'' and in
its place add ``054628''.
PART 522--IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS
0
21. The authority citation for 21 CFR part 522 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 522.1044 [Amended]
0
22. In paragraph (b)(3) of Sec. 522.1044, remove ``000010'' and in its
place add ``054628''.
Sec. 522.1222a [Amended]
0
23. In paragraph (b) of Sec. 522.1222a, remove ``000010, 000859,
061690, 026637, and 063286'' and in its place add ``000859, 026637,
054628, 061690, and 063286''.
Sec. 522.1410 [Amended]
0
24. In paragraph (b) of Sec. 522.1410, remove ``000010'' and in its
place add ``054628''.
Sec. 522.1662a [Amended]
0
25. In paragraphs (a)(2), (b)(2), (g)(2), and (h)(2) of Sec.
522.1662a, remove ``000010'' and in its place add ``054628''.
0
26. In Sec. 522.1680, revise the section heading to read as set forth
below; and in paragraph (b), remove ``000010, 000856, 000859, and
061623'' and in its place add ``000856, 000859, 054628, and 061623''.
Sec. 522.1680 Oxytocin.
* * * * *
0
27. In Sec. 522.1720, revise the section heading to read as set forth
below; and in paragraph (b)(2), remove ``000010'' and in its place add
``054628''.
Sec. 522.1720 Phenylbutazone.
* * * * *
0
28. In Sec. 522.2220, revise the section heading as set forth below;
and in paragraph (c)(2), remove ``000010'' and in its place add
``054628''.
Sec. 522.2220 Sulfadimethoxine.
* * * * *
0
29. In Sec. 522.2424, revise the section heading as set forth below;
and in paragraph (b), remove ``000010 and 000856'' and in its place add
``000856 and 054628''; and remove paragraph (c)(4).
Sec. 522.2424 Sodium thiamylal.
* * * * *
Sec. 522.2483 [Amended]
0
30. In paragraph (b) of Sec. 522.2483, remove ``000010'' and in its
place add ``054628''.
Sec. 522.2662 [Amended]
0
31. In paragraph (b)(1) of Sec. 522.2662, remove ``000010'' and in its
place add ``054628''.
PART 524--OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS
0
32. The authority citation for 21 CFR part 524 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 524.1580b [Amended]
0
33. In paragraph (b)(1) of Sec. 524.1580b, remove ``000010, 000069,
050749, 054925, 058005, and 061623'' and in its place add ``000069,
050749, 054628, 054925, 058005, and 061623''.
Sec. 524.1580c [Amended]
0
34. In paragraph (b) of Sec. 524.1580c, remove ``000010 and 000069''
and in its place add ``000069 and 054628''.
PART 526--INTRAMAMMARY DOSAGE FORM NEW ANIMAL DRUGS
0
35. The authority citation for 21 CFR part 526 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 526.1696b [Amended]
0
36. In paragraph (b) of Sec. 526.1696b, remove ``000010'' and in its
place add ``054628''.
PART 529--CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS
0
37. The authority citation for 21 CFR part 529 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 529.1044a [Amended]
0
38. In paragraph (b) of Sec. 529.1044a, remove ``000010, 000061,
000856, 000859 057561, 058005, and 061623'' and in its place add
``000061, 000856, 000859, 054628, 057561, 058005, and 061623''.
PART 558--NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
0
39. The authority citation for 21 CFR part 558 continues to read as
follows:
Authority: 21 U.S.C. 360b, 371.
Sec. 558.205 [Amended]
0
40. In paragraph (a) of Sec. 558.205, remove ``000010'' and in its
place add ``054628''.
Dated: March 26, 2013.
Steven D. Vaughn,
Director, Office of New Animal Drug Evaluation, Center for Veterinary
Medicine.
[FR Doc. 2013-07542 Filed 4-8-13; 8:45 am]
BILLING CODE 4160-01-P