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Implantation or Injectable Dosage Form New Animal Drugs; Change of Sponsor

---
identifier: "/us/fr/03-14547"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Implantation or Injectable Dosage Form New Animal Drugs; Change of Sponsor"
title_number: 0
title_name: "Federal Register"
section_number: "03-14547"
section_name: "Implantation or Injectable Dosage Form New Animal Drugs; Change of Sponsor"
positive_law: false
currency: "2003-06-10"
last_updated: "2003-06-10"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "03-14547"
document_type: "rule"
publication_date: "2003-06-10"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
cfr_references:
  - "21 CFR Part 522"
fr_citation: "68 FR 34533"
fr_volume: 68
effective_date: "2003-06-10"
fr_action: "Final rule."
---

#  [Amended]

**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 two approved new  animal drug applications (NADAs) from Anthony Products Co. to Cross Vetpharm Group Ltd.

**DATES:**

This rule is effective June 10, 2003.

**FOR FURTHER INFORMATION CONTACT:**

David R. Newkirk, Center for Veterinary Medicine (HFV-100), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 301-827-6967; e-mail: *[email protected]* .

**SUPPLEMENTARY INFORMATION:**

Anthony Products Co., 5600 Peck Rd., Arcadia, CA 91006, has informed FDA that it has transferred ownership of, and all rights and interest in, the following two approved NADAs to Cross Vetpharm Group, Ltd., Broomhill Rd., Tallaght, Dublin 24, Ireland:

| NADA Number | Trade Name |
| --- | --- |
| 065-505 | MICROCILLIN Injectable Suspension |
| 065-506 | COMBICILLIN Injectable Suspension |

Accordingly, the agency is amending the regulations in 21 CFR 522.1696a and 522.1696b 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 in 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 part 522 is amended as follows:

**PART 522—IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS**

**21 CFR Part 522**

1. The authority citation for 21 CFR part 522 continues to read as follows:

**Authority:**

21 U.S.C. 360b.

§ 522.1696a

**21 CFR Part 522**

2. Section 522.1696a *Penicillin G benzathine and penicillin G procaine sterile suspension* is amended in paragraph (b)(1) by removing “000864, 010515, and 049185” and by adding in its place “010515, 049185, and 061623”; and in paragraph (b)(3) by removing “000864, 010515, and 059130” and by adding in its place “010515, 059130, and 061623”.

§ 522.1696b

**21 CFR Part 522**

3. Section 522.1696b *Penicillin G procaine aqueous suspension* is amended in paragraph (b)(2) by removing “000864 and 055529” and by adding in its place “055529 and 061623”; in paragraph (d)(2)(i)(A) by removing “000864, 010515, 053501, and 059130” and by adding in its place “010515, 053501, 059130, and 061623”; and in paragraph (d)(2)(iii)(A) by removing “000864, 010515, 053501, and 059130” and by adding in its place “010515, 053501, and 059130”.

Dated: May 19, 2003.

Steven D. Vaughn,

Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.