2012-2103. New Animal Drugs; Chloramphenicol, Diethylcarbamazine Citrate, Hygromycin B, Methoxyflurane, Neomycin Sulfate, Penicillin G, Phenylbutazone, Pyrantel Tartrate, Tylosin Phosphate, and Sulfamethazine
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Start Preamble
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Final rule.
SUMMARY:
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect the withdrawal of approval of 20 new animal drug applications (NADAs).
DATES:
Withdrawal of approval is effective February 13, 2012.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
John Bartkowiak, Center for Veterinary Medicine (HFV-212),Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9079, email: john.bartkowiak@fda.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
The sponsors of the 20 approved NADAs listed in table 1 of this document have requested that FDA withdraw approval because the products are no longer manufactured or marketed:
Table 1—Voluntary Requests for Withdrawal of Approval (WOA) of 20 NADAs
Application No. Trade name (drug) Applicant NADA 014-485 METOPHANE Inhalation (methoxyflurane) Medical Developments, International, Ltd., P.O. Box 21, Sandown Village, 3171 VIC Australia. NADA 032-322 LIQUISONE F with Cerumene (hexamethyltetracosane, prednisolone, tetracaine, neomycin sulfate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 044-655 NEOMYCANE Ophthalmic Ointment (neomycin sulfate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 045-288 OPTISONE (neomycin sulfate, prednisolone acetate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 049-890 NORCO T-2 Pre-Pak (tylosin phosphate) Norco Mills of Norfolk, Inc., P.O. Box 56, Norfolk, NE 68701. NADA 055-034 CHLORASOL (chloramphenicol) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 055-052 Chlora-Tabs 100 (chloramphenicol) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 065-158 CHLORICOL (chloramphenicol) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 065-259 CHLORASONE Ophthalmic Ointment (chloramphenicol, prednisolone acetate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. Start Printed Page 4896 NADA 065-488 BENZA-PEN (penicillin G benzathine, penicillin G procaine) Walco International, Inc., 15 West Putnam, Porterville, CA 93257. NADA 095-953 MOORMABOOST TY 4000 Medicated (tylosin phosphate) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 100-689 DIFIL Syrup (diethylcarbamazine citrate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 100-690 DIFIL Tablets (diethylcarbamazine citrate) Evsco Pharmaceuticals, an Affiliate of IGI, Inc., Box 209, Harding Hwy., Buena, NJ 08310. NADA 107-957 TYLAN 20 Sulfa-G (tylosin phosphate and sulfamethazine) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 111-069 TYLAN 40 Sulfa-G (tylosin phosphate and sulfamethazine) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 131-956 TYLAN Sulfa-G (tylosin phosphate and sulfamethazine) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 131-957 TYLAN 40 (tylosin phosphate) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 133-490 Ban-D-Wormer II BANMINTH (pyrantel tartrate) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 140-842 HYGROMIX 2.4 Premix (hygromycin B) ADM Alliance Nutrition, Inc., 1000 North 30th St., Quincy, IL 62305-3115. NADA 140-958 EQUIPHEN Paste (phenylbutazone) 520.1720c Luitpold Pharmaceuticals, Inc., Animal Health Division, Shirley, NY 11967. In a notice published elsewhere in this issue of the Federal Register, FDA gave notice that approval of NADAs 014-485, 032-322, 044-655, 045-288, 049-890, 055-034, 055-052, 065-158, 065-259, 065-488, 095-953, 100-689, 100-690, 107-957, 111-069, 131-956, 131-957, 133-490, 140-842, and 140-958, and all supplements and amendments thereto, is withdrawn, effective February 13, 2012. As provided in the regulatory text of this document, the animal drug regulations are amended to reflect these withdrawals of approval and a current format.
Following these withdrawals of approval, Evsco Pharmaceuticals, an Affiliate of IGI, Inc.; Medical Developments International, Ltd.; and Norco Mills of Norfolk, Inc., are no longer the sponsor of an approved application. Accordingly, 21 CFR 510.600(c) is being amended to remove the entries for these firms.
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.
Start List of SubjectsList of Subjects
21 CFR Part 510
- Administrative practice and procedure
- Animal drugs
- Labeling
- Reporting and recordkeeping requirements
21 CFR Part 520, 522, 524, and 529
- Animal drugs
21 CFR Part 558
- Animal drugs
- Animal feeds
Therefore, under the Federal Food, Drug, and Cosmetic Act and under the authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, 21 CFR parts 510, 520, 522, 524, 529, and 558 are amended as follows:
Start PartPART 510—NEW ANIMAL DRUGS
End Part Start Amendment Part1. The authority citation for 21 CFR part 510 continues to read as follows:
End Amendment Part[Amended]2. In § 510.600, in the table in paragraph (c)(1), remove the entries for “Evsco Pharmaceuticals, An Affiliate of IGI, Inc.”, “Medical Developments International, Ltd.”, and “Norco Mills of Norfolk, Inc.”; and in the table in paragraph (c)(2), remove the entries for “017030”, “025245”, and “027190”.
End Amendment Part Start PartPART 520—ORAL DOSAGE FORM NEW ANIMAL DRUGS
End Part Start Amendment Part3. The authority citation for 21 CFR part 520 continues to read as follows:
End Amendment Part Start Amendment Part4. Revise § 520.390a to read as follows:
End Amendment PartChloramphenicol tablets.(a) Specifications. Each tablet contains 50, 100, 250, or 500 milligrams (mg); 1 or 2.5 grams (g) of chloramphenicol.
(b) Sponsors. See § 510.600(c) of this chapter:
(1) For use as in paragraphs (c)(1), (c)(2)(i), and (c)(3) of this section:
(i) No. 000010 for 100-, 250-, and 500-mg; and 1- and 2.5-g tablets;
(ii) No. 000856 for 100-, 250-, and 500-mg tablets;
(iii) No. 000069 for 250-mg tablets.
(2) For use as in paragraphs (c)(1), (c)(2)(ii), and (c)(3) of this section:
(i) No. 061623 for 50-, 100-, 250-, and 500-mg; and 1-g tablets;
(ii) [Reserved]
(c) Conditions of use in dogs—(1) Amount. Administer 25 mg per pound of body weight by mouth every 6 hours.
(2) Indications for use—(i) For the treatment of bacterial pulmonary infections, bacterial infections of the urinary tract, bacterial enteritis, and bacterial infections associated with canine distemper caused by susceptible organisms.
(ii) For the treatment of bacterial gastroenteritis associated with bacterial diarrhea, bacterial pulmonary infections, and bacterial infections of the urinary tract caused by susceptible organisms.
(3) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law prohibits the extralabel use of this drug in food-producing animals.
[Amended]5. In § 520.622a, remove and reserve paragraph (a)(4).
End Amendment Part Start Amendment Part6. In § 520.622b, remove and reserve paragraph (b).
End Amendment Part[Amended]7. In § 520.1720c, in paragraph (b)(1), remove “Nos. 000061 and 010797” and in its place add “No. 000061”.
End Amendment Part Start PartPART 522—IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS
End Part Start Amendment Part8. The authority citation for 21 CFR part 522 continues to read as follows:
End Amendment Part Start Amendment Part9. In § 522.1696a, revise paragraphs (b)(1), (b)(3), (d)(1)(iii), and (d)(2)(iii) to read as follows:
End Amendment PartPenicillin G benzathine and penicillin G procaine suspension.* * * * *(b) * * *
(1) Nos. 000856, 055529, and 061623 for use as in paragraph (d)(1) of this section.
* * * * *(3) No. 000856 for use as in paragraphs (d)(2)(i), (d)(2)(ii)(B), and (d)(2)(iii) of this section.
* * * * *(d) * * *
(1) * * *
(iii) Limitations. Not for use in beef cattle within 30 days of slaughter. Do not use in horses intended for human consumption. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
(2) * * *
(iii) Limitations. Not for use within 30 days of slaughter. For Nos. 055529, 059130, and 061623: A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.
PART 524—OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS
End Part Start Amendment Part10. The authority citation for 21 CFR part 524 continues to read as follows:
End Amendment Part Start Amendment Part11. Revise § 524.390 to read as follows:
End Amendment PartChloramphenicol ophthalmic ointment.(a) Specifications. Each gram contains 10 milligrams chloramphenicol.
(b) Sponsors. See Nos. 000856 and 025463 in § 510.600(c) of this chapter.
(c) Conditions of use in dogs and cats—(1) Amount. Apply every 3 hours around the clock for 48 hours, after which night instillations may be omitted.
(2) Indications for use. For treatment of bacterial conjunctivitis caused by pathogens susceptible to chloramphenicol.
(3) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
§§ 524.390a, 524.390b, and 524.390d [Removed]
12. Remove §§ 524.390a, 524.390b, and 524.390d.
End Amendment Part§§ 524.1484a, 524.1484j, and 524.1484k [Removed]
Start Amendment Part13. Remove 524.1484a, 524.1484j, and 524.1484k.
End Amendment Part§§ 524.1880 [Removed]
Start Amendment Part14. Remove 524.1880.
End Amendment Part Start PartPART 529—CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS
End Part Start Amendment Part15. The authority citation for 21 CFR part 529 continues to read as follows:
End Amendment Part[Removed]16. Remove 529.1455.
End Amendment Part Start PartPART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
End Part Start Amendment Part17. The authority citation for 21 CFR part 558 continues to read as follows:
End Amendment Part[Amended]18. In § 558.274, remove and reserve paragraph (a)(7); and in the table in paragraphs (c)(1)(i) and (c)(1)(ii), in the “Sponsor” column, remove “012286”.
End Amendment Part[Amended]19. In paragraph (b)(3) of § 558.485, remove “012286”.
End Amendment Part[Amended]20. In § 558.625, remove and reserve paragraphs (b)(10), (b)(12), and (b)(67).
End Amendment Part[Amended]21. In § 558.630, remove and reserve paragraph (b)(2) and in paragraph (b)(5), remove “012286”.
End Amendment Part Start SignatureDated: January 26, 2012.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. 2012-2103 Filed 1-31-12; 8:45 am]
BILLING CODE 4160-01-P
Document Information
- Effective Date:
- 2/13/2012
- Published:
- 02/01/2012
- Department:
- Food and Drug Administration
- Entry Type:
- Rule
- Action:
- Final rule.
- Document Number:
- 2012-2103
- Dates:
- Withdrawal of approval is effective February 13, 2012.
- Pages:
- 4895-4897 (3 pages)
- Docket Numbers:
- Docket No. FDA-2011-N-0003
- Topics:
- Administrative practice and procedure, Animal drugs, Animal feeds, Labeling, Reporting and recordkeeping requirements
- PDF File:
- 2012-2103.pdf
- Supporting Documents:
- » Freedom of Information Summary NADA 141-324 Phenylpropanolamine
- » Freedom of Information Summary NADA 141-331 Pergolide
- » Freedom of Information Summary NADA 141-333 - Milbemycin Oxime, Lufenuron, and Praziquantel
- » Freedom of Information Summary NADA 095-735 - Monensin
- » Freedom of Information Summary NADA 141-207 - Danofloxacin
- » Freedom of Information Summary NADA 141-322 - Gonadotropin Releasing Factor Analog-Diphtheria Toxoid Conjugate
- » Freedom of Information Summary ANDA 200-494 - Gentamicin Sulfate
- » reedom of Information Summary NADA 141-203 Deracoxib
- » Gentamicin Topical Spray (gentamicin sulfate, betamethasone valerate- ANADA 200-416; Freedom of Information Summary
- » Freedom of Information Summary ANDA 200-318 Bimectin Pour-On (Ivermectin)
- CFR: (12)
- 21 CFR 510.600
- 21 CFR 524.390
- 21 CFR 529.1455
- 21 CFR 558.274
- 21 CFR 558.485
- More ...