[Federal Register: June 27, 2002 (Volume 67, Number 124)]
[Rules and Regulations]
[Page 43247-43248]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27jn02-9]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 510 and 520
New Animal Drugs; Change of Sponsor
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
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SUMMARY: The Food and Drug Administration (FDA) is amending the animal
drug regulations to reflect a change of sponsor for two approved new
animal drug applications (NADAs) and an approved abbreviated new animal
drug application (ANADA) from Lambert-Kay, A Division of Carter-
Wallace, Inc., to Church & Dwight Co., Inc. The drug labeler code for
Church & Dwight Co., Inc., is also being listed.
DATES: This rule is effective June 27, 2002.
FOR FURTHER INFORMATION CONTACT: Lonnie W. Luther, Center for
Veterinary Medicine (HFV-101), Food and Drug Administration, 7500
Standish Pl., Rockville, MD 20855, 301-827-0209, e-mail:
lluther@cvm.fda.gov.
SUPPLEMENTARY INFORMATION: Lambert-Kay, A Division of Carter-Wallace,
Inc., P.O. Box 1001, Half Acre Rd., Cranbury, NJ 08512-0181, has
informed FDA that it has transferred ownership of, and all rights and
interest in, NADA 101-497 for TINY TIGER (dichlorophene/toluene)
Worming Capsules, NADA 101-498 for LK (dichlorophene/toluene) Worming
Capsules, and ANADA 200-028 for EVICT (pyrantel pamoate) Liquid Wormer
to Church & Dwight Co., Inc., 469 North Harrison St., Princeton, NJ
08543-5297. Accordingly, the agency is amending the regulations in
Secs. 520.580 and 520.2043 (21 CFR 520.580 and 520.2043) to reflect the
transfer of ownership.
Church & Dwight Co., Inc., has not been previously listed in the
animal drug regulations as a sponsor of an approved application.
Following these changes of sponsorship, Lambert-Kay is no longer the
sponsor of any approved applications. Accordingly, 21 CFR 510.600(c)(1)
and (c)(2) is being amended to add entries for Church & Dwight Co.,
Inc., and to remove the entries for Lambert-Kay. Also, Sec. 520.2043 is
being revised to reflect a current format.
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 Part 520
Animal drugs.
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 and
520 are amended as follows:
PART 510--NEW ANIMAL DRUGS
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.
2. Section 510.600 is amended in the table in paragraph (c)(1) by
removing the entry for ``Lambert-Kay, A Division of Carter-Wallace,
Inc.'' and by alphabetically adding an entry for ``Church & Dwight Co.,
Inc.'' and in the table in paragraph (c)(2) by removing the entry
``011615'' and by numerically adding an entry for ``010237'' to read as
follows:
[[Page 43248]]
Sec. 510.600 Names, addresses, and drug labeler codes of sponsors of
approved applications.
* * * * *
(c) * * *
(1) * * *
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Firm name and address Drug labeler code
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* * * * * *
*
Church & Dwight Co., Inc., 469 North Harrison St., 010237
Princeton, NJ 08543-5297
* * * * * *
*
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(2) * * *
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Drug labeler code Firm name and address
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* * * *
* * *
010237 Church & Dwight Co., Inc., 469 North Harrison
St., Princeton, NJ 08543-5297
* * * *
* * *
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PART 520--ORAL DOSAGE FORM NEW ANIMAL DRUGS
3. The authority citation for 21 CFR part 520 continues to read as
follows:
Authority: 21 U.S.C. 360b.
Sec. 520.580 [Amended]
4. Section 520.580 Dichlorophene and toluene capsules is amended by
removing footnote 1 every place it appears in the section and in
paragraph (b)(1) by removing ``011615'' and by adding in its place
``010237''.
5. Section 520.2043 is revised to read as follows:
Sec. 520.2043 Pyrantel pamoate suspension.
(a) Specifications. (1) Each milliliter (mL) contains pyrantel
pamoate equivalent to 50 milligrams (mg) pyrantel base.
(2) Each mL contains pyrantel pamoate equivalent to 2.27 or 4.54 mg
pyrantel base.
(3) Each mL contains pyrantel pamoate equivalent to 4.54 mg
pyrantel base.
(b) Sponsors. See sponsors in Sec. 510.600(c) of this chapter for
uses as in paragraph (d) of this section.
(1) Nos. 000069 and 059130 for use of the product described in
paragraph (a)(1) as in paragraph (d)(1) of this section.
(2) Nos. 000069, 010237, and 059130 for use of the products
described in paragraph (a)(2) as in paragraph (d)(2) of this section.
(3) No. 023851 for use of the product described in paragraph (a)(3)
as in paragraph (d)(2) of this section.
(c) Special considerations. See Sec. 500.25 of this chapter.
(d) Conditions of use--(1) Horses and ponies. It is used as
follows:
(i) Amount. 3 mg per pound (/lb) body weight as a single dose mixed
with the usual grain ration, or by stomach tube or dose syringe.
(ii) Indications for use. For the removal and control of infections
from the following mature parasites: Large strongyles (Strongylus
vulgaris, S. edentatus, S. equinus), small strongyles, pinworms
(Oxyuris), and large roundworms (Parascaris).
(iii) Limitations. Not for use in horses and ponies to be
slaughtered for food purposes. When the drug is for administration by
stomach tube, it shall be labeled: ``Federal law restricts this drug to
use by or on the order of a licensed veterinarian.''
(2) Dogs. It is used as follows:
(i) Dogs and puppies--(A) Amount. 2.27 mg/lb body weight as a
single dose in the animal's feed bowl by itself or mixed in a small
quantity of food.
(B) Indications for use. For the removal of large roundworms
(Toxocara canis and Toxascarias leonina) and hookworms (Ancylostoma
caninum and Uncinaria stenocephala).
(C) Limitations. Additional treatment may be required and should be
confirmed by fecal examination within 2 to 4 weeks.
(ii) Dogs, puppies, and lactating bitches after whelping--(A)
Amount. 2.27 mg/lb body weight.
(B) Indications for use. To prevent reinfections of T. canis.
(C) Limitations. Administer to puppies at 2, 3, 4, 6, 8, and 10
weeks of age. Administer to lactating bitches 2 to 3 weeks after
whelping. Adult dogs kept in heavily contaminated quarters may be
treated at monthly intervals.
Dated: May 24, 2002.
Andrew J. Beaulieu,
Acting Director, Office of New Animal Drug Evaluation, Center for
Veterinary Medicine.
[FR Doc. 02-16050 Filed 6-26-02; 8:45 am]
BILLING CODE 4160-01-S