2013-20616. Withdrawal of Approval of New Animal Drug Applications; Quali-Tech Products, Inc.; Bambermycins; Pyrantel; Tylosin; Virginiamycin
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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 four new animal drug applications (NADAs), held by Quali-Tech Products, Inc., at the sponsor's request because the products are no longer manufactured or marketed.
DATES:
The rule is effective September 3, 2013.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
David Alterman, Center for Veterinary Medicine (HFV-212), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-453-6843, david.alterman@fda.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
Quali-Tech Products, Inc., has requested that FDA withdraw approval of the following four NADAs because the products, used to manufacture Type C medicated feeds, are no longer manufactured or marketed: NADA 097-980 for Quali-Tech TYLAN-10 (tylosin phosphate) Premix, NADA 118-815 for Q.T. BAN-TECH (pyrantel tartrate), NADA 132-705 for FLAVOMYCIN (bambermycins), and NADA 133-335 for STAFAC (virginiamycin) Swine Pak 10.
Elsewhere in this issue of the Federal Register, FDA gave notice that approval of NADAs 097-980, 118-815, 132-705, and 133-335, and all supplements and amendments thereto, is withdrawn. As provided in the regulatory text of this document, the animal drug regulations are amended to reflect these voluntary withdrawals of approval.
Following these withdrawals of approval, Quali-Tech Products, Inc., will no longer be the sponsor of an approved application. Accordingly, 21 CFR 510.600(c) is being amended to remove the entries for this firm.
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 Parts 558
- Animal drugs
- Animal feeds
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 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 entry for “Quali-Tech Products, Inc.”; and in the table in paragraph (c)(2), remove the entry for “016968”.
End Amendment Part Start PartPART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
End Part Start Amendment Part3. The authority citation for 21 CFR part 558 continues to read as follows:
End Amendment Part Start Amendment Part4. In § 558.95, revise paragraphs (a), (d)(1), (d)(2), (d)(3), (d)(4)(i), and (d)(4)(ii) to read as follows:
End Amendment PartBambermycins.(a) Approvals. See sponsors in § 510.600(c) of this chapter for use of Type A medicated articles as in paragraph (d) of this section:
(1) No. 016592: 2, 4, and 10 grams per pound for use as in paragraphs (d)(1), (d)(2), (d)(3), and (d)(4) of this section.
(2) Nos. 012286 and 017790: 2 grams for use as in paragraph (d)(2) of this section and 0.4 and 2 grams per pound for use as in paragraph (d)(3).
* * * * *(d) * * *
(1) Chickens. Use in medicated feed as follows:
Bambermycins in grams/ton Indications for use Limitations Sponsor (i) 1 to 2 Broiler chickens: For increased rate of weight gain and improved feed efficiency Feed continuously as the sole ration 016592. (ii) [Reserved] (2) Turkeys. Use in medicated feed as follows:
Start Printed Page 52431Bambermycins in grams/ton Indications for use Limitations Sponsor (i) 1 to 2 Growing turkeys: For improved feed efficiency Feed continuously as the sole ration 012286, 016592, 017790. (ii) 2 Growing turkeys: For increased rate of weight gain and improved feed efficiency Feed continuously as the sole ration 012286, 016592, 017790. (3) Swine. Use in medicated feed as follows:
Bambermycins in grams/ton Indications for use Limitations Sponsor (i) 2 Growing-finishing swine: For increased rate of weight gain and improved feed efficiency Feed continuously as the sole ration 012286, 016592, 017790. (ii) 2 to 4 Growing-finishing swine: For increased rate of weight Feed continuously as the sole ration 012286, 016592, 017790. (4) Cattle. Use in medicated feed as follows:
Bambermycins in grams/ton Indications for use Limitations Sponsor (i) 1 to 4 Cattle fed in confinement for slaughter: For increased rate of weight gain and improved feed efficiency Feed continuously at a rate of 10 to 20 milligrams per head per day 016592. (ii) 2 to 40 Pasture cattle (slaughter, stocker, and feeder cattle, and dairy and beef replacement heifers): For increased rate of weight gain Feed continuously at a rate of 10 to 40 milligrams per head per day in at least 1 pound and not more than 10 pounds of feed. Daily bambermycins intakes in excess of 20 mg/head/day have not been shown to be more effective than 20 mg/head/day 016592. * * * * *[Amended]5. In paragraph (b)(3) of § 558.485, remove “Nos. 016968, and 017790” and in its place add “No. 017790”.
End Amendment Part[Amended]6. In § 558.625, remove and reserve paragraph (b)(14).
End Amendment Part[Amended]7. In paragraph (a)(2) of § 558.635, remove “046573, 016968, and 017790” and in its place add “046573 and 017790”.
End Amendment Part Start SignatureDated: August 20, 2013.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. 2013-20616 Filed 8-22-13; 8:45 am]
BILLING CODE 4160-01-P
Document Information
- Effective Date:
- 9/3/2013
- Published:
- 08/23/2013
- Department:
- Food and Drug Administration
- Entry Type:
- Rule
- Action:
- Final rule.
- Document Number:
- 2013-20616
- Dates:
- The rule is effective September 3, 2013.
- Pages:
- 52430-52431 (2 pages)
- Docket Numbers:
- Docket No. FDA-2013-N-0002
- Topics:
- Administrative practice and procedure, Animal drugs, Animal feeds, Labeling, Reporting and recordkeeping requirements
- PDF File:
- 2013-20616.pdf
- Supporting Documents:
- » FREEDOM OF INFORMATION SUMMARY NADA 130-185 AMPROL 25% and FLAVOMYCIN Amprolium and Bambermycins
- » FREEDOM OF INFORMATION SUMMARY Application Number 141-422 PACCAL VET-CA1 Paclitaxel for injection Powder for Injection Dog
- » FREEDOM OF INFORMATION SUMMARY NADA141-420 TILDREN tiludronate disodium Powder for injection Horse
- » FREEDOM OF INFORMATION SUMMARY NADA 141-361 PULMOTIL AC Tilmicosin Phosphate Aqueous Concentrate Swine
- » FREEDOM OF INFORMATION SUMMARY NADA 141-246 AQUAFLOR Florfenicol
- » Freedom of Information Summary NADA 141-288 EXCENEL RTU EZ Ceftiofur Hydrochloride
- » Freedom of Information Summary NADA 095-735 RUMENSIN 90 Monensin
- » Freedom of Information Summary NADA 141-406 NEXGARD Afoxolaner Chewable Tablet
- » Freedom of Information Summary ANADA 200-548 ACTOGAIN 45 Ractopamine Hydrochloride Cattle fed in confinement for slaughter
- » Freedom of Information Summary ANADA 200-542 ENGAIN 9 and ENGAIN 5 Ractopamine Hydrochloride Finishing Swine
- CFR: (5)
- 21 CFR 510.600
- 21 CFR 558.95
- 21 CFR 558.485
- 21 CFR 558.625
- 21 CFR 558.635