New Animal Drugs; Change of Sponsor; Zinc Gluconate
Federal Register, Volume 76 Issue 245 (Wednesday, December 21, 2011)
Federal Register Volume 76, Number 245 (Wednesday, December 21, 2011)
Rules and Regulations
Page 79064
From the Federal Register Online via the Government Printing Office www.gpo.gov
FR Doc No: 2011-32591
Page 79064
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 510 and 522
Docket No. FDA-2011-N-0003
New Animal Drugs; Change of Sponsor; Zinc Gluconate
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 a new animal drug application (NADA) for zinc gluconate injectable solution from Technology Transfer, Inc., to Ark Sciences, Inc.
DATES: This rule is effective December 21, 2011.
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: Technology Transfer, Inc., 33 East Broadway, suite 190, Columbia, MO 65203 has informed FDA that it has transferred ownership of, and all rights and interest in, NADA 141-217 for NEUTERSOL (zinc gluconate) Injectable Solution to Ark Sciences, Inc., 1101 East 33rd St., suite B304, Baltimore, MD 21218. Accordingly, the Agency is amending the regulations in 21 CFR 522.2690 to reflect the transfer of ownership.
Following this change of sponsorship, Technology Transfer, Inc., is no longer the sponsor of an approved application. Accordingly, Sec. 510.600 (21 CFR 510.600) is being amended to remove the entries for this firm.
In addition, Ark Sciences, Inc., is not currently listed in the animal drug regulations as a sponsor of an approved application. Accordingly, Sec. 510.600 is being amended to add entries for this sponsor.
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
Administrative practice and procedure, Animal drugs, Labeling, Reporting and recordkeeping requirements.
21 CFR Part 522
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 522 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.
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2. In Sec. 510.600, in the table in paragraph (c)(1), remove the entry for ``Technology Transfer, Inc.''; alphabetically add a new entry for ``Ark Sciences, Inc.''; and in the table in paragraph (c)(2), remove the entry for ``067647''; and in numerical sequence add a new entry for ``076175'' to read as follows:
Sec. 510.600 Names, addresses, and drug labeler codes of sponsors of approved applications.
* * * * *
(c) * * *
(1) * * *
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Drug
Firm name and address labeler
code
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* * * * *
Ark Sciences, Inc., 1101 East 33rd St., suite B304, 076175
Baltimore, MD 21218.......................................
* * * * *
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(2) * * *
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Drug labeler code Firm name and address
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* * * * *
076175............................ Ark Sciences, Inc., 1101 East 33rd
St., suite B304, Baltimore, MD
21218.
* * * * *
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PART 522--IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS
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3. The authority citation for 21 CFR part 522 continues to read as follows:
Authority: 21 U.S.C. 360b.
Sec. 522.2690 Amended
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4. In paragraph (b) of Sec. 522.2690, remove ``067647'' and in its place add ``076175''.
Dated: December 8, 2011.
Steven D. Vaughn,
Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.
FR Doc. 2011-32591 Filed 12-20-11; 8:45 am
BILLING CODE 4160-01-P
