# [Amended]
**AGENCY:**
Food and Drug Administration, HHS.
**ACTION:**
Final rule; technical amendment.
**SUMMARY:**
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval actions for new animal drug applications (NADAs) and abbreviated new animal drug applications (ANADAs) during December 2012. FDA is also informing the public of the availability of summaries of the basis of approval and of environmental review documents, where applicable.
**DATES:**
This rule is effective January 28, 2013.
**FOR FURTHER INFORMATION CONTACT:**
George K. Haibel, Center for Veterinary Medicine (HFV-6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9019, *[email protected].*
**SUPPLEMENTARY INFORMATION:**
FDA is amending the animal drug regulations to reflect approval actions for several original ANADAs during December 2012, as listed in table 1. In addition, FDA is informing the public of the availability, where applicable, of documentation of environmental review required under the National Environmental Policy Act (NEPA) and, for actions requiring review of safety or effectiveness data, summaries of the basis of approval (FOI Summaries) under the Freedom of Information Act (FOIA). These public documents may be seen in the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852, between 9 a.m. and 4 p.m., Monday through Friday. Persons with access to the Internet may obtain these documents at the Center for Veterinary Medicine FOIA Electronic Reading Room: *http://www.fda.gov/AboutFDA/CentersOffices/OfficeofFoods/CVM/CVMFOIAElectronicReadingRoom/default.htm.*
| NADA/ANADA | Sponsor | New animal drug product name | Action | 21 CFR section | FOIA summary | NEPA review |
| --- | --- | --- | --- | --- | --- | --- |
| 200-485 | Accord Healthcare, Inc., 1009 Slater Rd., suite 210-B, Durham, NC 27703 | Meloxicam Injection | Original approval as a generic copy of NADA 141-219 | 522.1367 | yes | CE |
| 200-491 | Norbrook Laboratories, Ltd., Station Works, Newry BT35 6JP, Northern Ireland | LOXICOM (meloxicam) Solution for Injection | Original approval as a generic copy of NADA 141-219 | 522.1367 | yes | CE |
| 200-543 | Putney, Inc., 400 Congress St., suite 200, Portland, ME 04101 | Cefpodoxime Proxetil Tablets | Original approval as a generic copy of NADA 141-232 | 520.370 | yes | CE |
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.
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, 520, and 522 are 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**
§ 510.600
2. In § 510.600, in the table in paragraph (c)(1), alphabetically add an entry for “Accord Healthcare, Inc.” and revise the entry for “Jurox Pty. Ltd.”; and in the table in paragraph (c)(2), numerically add an entry for “016729” and revise the entry for “049480” to read as follows:
(1) * * *
| Firm name and address | Drug |
| --- | --- |
| | |
| * * * * * | |
| Accord Healthcare, Inc., 1009 Slater Rd., suite 210-B, Durham, NC 27703 | 016729 |
| | |
| * * * * * | |
| Jurox Pty. Ltd., 85 Gardiner St., Rutherford, NSW 2320, Australia | 049480 |
| | |
| * * * * * | |
(2) * * *
| Drug labeler code | Firm name and address |
| --- | --- |
| | |
| * * * * * | |
| 016729 | Accord Healthcare, Inc., 1009 Slater Rd., suite 210-B, Durham, NC 27703 |
| | |
| * * * * * | |
| 049480 | Jurox Pty. Ltd., 85 Gardiner St., Rutherford, NSW 2320, Australia |
| | |
| * * * * * | |
**21 CFR Part 520**
**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.
**21 CFR Part 520**
§ 520.370
4. In paragraph (b) of § 520.370, remove “No. 000009” and in its place add “Nos. 000009 and 026637”.
**21 CFR Part 522**
**PART 522—IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS**
5. The authority citation for 21 CFR part 522 continues to read as follows:
**Authority:**
21 U.S.C. 360b.
**21 CFR Part 522**
§ 522.1367
6. In paragraph (b) of § 522.1367, remove “No. 000010” and in its place add “Nos. 000010, 016729, and 055529”.
Dated: January 22, 2013.
Bernadette Dunham,
Director, Center for Veterinary Medicine.