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New Animal Drugs; Change of Sponsor's Name

---
identifier: "/us/fr/2012-13409"
source: "fr"
legal_status: "authoritative_unofficial"
title: "New Animal Drugs; Change of Sponsor's Name"
title_number: 0
title_name: "Federal Register"
section_number: "2012-13409"
section_name: "New Animal Drugs; Change of Sponsor's Name"
positive_law: false
currency: "2012-06-04"
last_updated: "2012-06-04"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2012-13409"
document_type: "rule"
publication_date: "2012-06-04"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
cfr_references:
  - "21 CFR Part 510"
fr_citation: "77 FR 32897"
fr_volume: 77
docket_ids:
  - "Docket No. FDA-2012-N-0002"
effective_date: "2012-06-04"
fr_action: "Final rule."
---

#  Names, addresses, and drug labeler codes of sponsors of approved applications.

**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's name from Novopharm Ltd. to Teva Canada Ltd.

**DATES:**

This rule is effective June 4, 2012.

**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: *[email protected].*

**SUPPLEMENTARY INFORMATION:**

Novopharm Ltd., 30 Novopharm Ct., Toronto, Ontario, Canada M1B 2K9 has informed FDA of a change of name to Teva Canada Ltd. Accordingly, the Agency is amending the regulations in 21 CFR 510.600(c) to reflect these changes.

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 510**

Administrative practice and procedure, Animal drugs, Labeling, Reporting and recordkeeping requirements.

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 510 is amended as follows:

**21 CFR Part 510**

**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.

**21 CFR Part 510**

2. In § 510.600, in the table in paragraph (c)(1), remove the entry for “Novopharm Ltd.” and alphabetically add a new entry for “Teva Canada Ltd.”; and in the table in paragraph (c)(2), revise the entry for “043806” to read as follows:

§ 510.600

(c) * * *

(1) * * *

| Firm name and address | Drug |
| --- | --- |
|  |  |
| *    *    *    *    * |  |
| Teva Canada Ltd., 30 Novopharm Ct., Toronto, Ontario, Canada M1B 2K9 | 043806 |
|  |  |
| *    *    *    *    * |  |

(2) * * *

| Drug labeler code | Firm name and |
| --- | --- |
|  |  |
| *    *    *    *    * |  |
| 043806 | Teva Canada Ltd., 30 Novopharm Ct., Toronto, Ontario, Canada M1B 2K9. |
|  |  |
| *    *    *    *    * |  |

Dated: May 29, 2012.

Bernadette Dunham,

Director, Center for Veterinary Medicine.