94-3714. American Cyanamid Co.; Withdrawal of Approval of NADA
[Federal Register Volume 59, Number 34 (Friday, February 18, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-3714]
[[Page Unknown]]
[Federal Register: February 18, 1994]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 93N-0471]
American Cyanamid Co.; Withdrawal of Approval of NADA
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is withdrawing approval
of a new animal drug application (NADA) held by American Cyanamid Co.
The NADA provides for the use of maduramicin ammonium in combination
with chlortetracycline in the feed of broiler chickens for prevention
of coccidiosis and as an aid in the reduction of mortality due to
Escherichia coli infections. The firm requested the withdrawal of the
approval of the NADA. In a final rule published elsewhere in this issue
of the Federal Register, FDA is amending the regulations by removing
the portion of the regulation which reflects approval of the NADA.
EFFECTIVE DATE: February 28, 1994.
FOR FURTHER INFORMATION CONTACT: Mohammad I. Sharar, Center for
Veterinary Medicine (HFV-216), Food and Drug Administration, 7500
Standish Pl., Rockville MD 20855, 301-594-0749.
SUPPLEMENTARY INFORMATION: American Cyanamid Co., Agricultural Research
Division, Box 400, Princeton, NJ 08450, is the sponsor of NADA 140-837
that provides for the use of 4.54 to 5.45 grams (g) per ton of
maduramicin ammonium combination with 500 g per ton of
chlortetracycline in the feed of broiler chickens for the prevention of
coccidiosis and as an aid in the reduction of mortality due to E. coli
infections. American Cyanamid requested withdrawal of the NADA
approval.
Therefore, under authority delegated to the Commissioner of Food
and Drugs (21 CFR 5.10) and redelegated to the Center for Veterinary
Medicine (21 CFR 5.84), and in accordance with Sec. 514.115 Withdrawal
of approval of applications (21 CFR 514.115), notice is given that
approval of NADA 140-837 and all supplements and amendments thereto is
hereby withdrawn, effective February 28, 1994.
In a final rule published elsewhere in this issue of the Federal
Register, FDA is amending 21 CFR 558.128(c)(5)(xiii) and 558.340(c)(2)
to reflect withdrawal of the approval.
Dated: February 9, 1994.
Richard H. Teske,
Acting Director, Center for Veterinary Medicine.
[FR Doc. 94-3714 Filed 2-17-94; 8:45 am]
BILLING CODE 4160-01-F
Document Information
- Published:
- 02/18/1994
- Department:
- Food and Drug Administration
- Entry Type:
- Uncategorized Document
- Action:
- Notice.
- Document Number:
- 94-3714
- Dates:
- February 28, 1994.
- Pages:
- 0-0 (1 pages)
- Docket Numbers:
- Federal Register: February 18, 1994, Docket No. 93N-0471