CORID- amprolium granule

CORID by

Drug Labeling and Warnings

CORID by is a Animal medication manufactured, distributed, or labeled by Huvepharma, Inc, Huvepharma EOOD, Huvepharma, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS

An aid in the prevention and treatment of coccidiosis caused by Eimeria bovis and E. zurnii in calves.

WARNING

Keep this and all drugs out of the reach of children. NOT FOR HUMAN USE.

The Material Safety Data Sheet (MSDS) contains more detailed occupational safety information. To report adverse effects, obtain an MSDS or for assistance, contact 1-888-994-4883

RESIDUE WARNING

Withdraw 24 hours before slaughter. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

CAUTION

For satisfactory diagnosis, a microscopic examination of the feces should be done by a veterinarian or diagnostic laboratory before treatment. When treating outbreaks, drug should be administered promptly after diagnosis is determined.

Do not use in feeds containing bentonite.
Use as the sole source of amprolium.
Restricted Drug – Use only as directed (California).

MIXING DIRECTIONS

CORID 25% should be thoroughly and evenly mixed in the feed. CORID 25% may be used to manufacture a Type B medicated feed with a concentration of 2.5% amprolium or a Type C medicated feed in the concentration range of 0.0125% to 1.25% amprolium.

• Use 200 pounds of CORID 25% per ton of feed to produce Type B medicated feed containing 2.5% amprolium.
• Use 1 pound of CORID 25% per ton of feed to produce Type C medicated feed containing 0.0125% amprolium.1
• Use 100 pounds of CORID 25% per ton of feed to produce Type C medicated feed containing 1.25% amprolium.
• Use 10 pounds of 2.5% Type B per ton of feed to produce Type C medicated feed containing 0.0125% amprolium.
• Use 1000 pounds of 2.5% Type B per ton of feed to produce Type C medicated feed containing 1.25% amprolium.

1 To aid in even distribution of CORID 25% in the finished feed, prepare a mixture of CORID 25% in a portion of complete feed ingredient before mixing into the finished ration. Blend the mixture with the remainder of the finished feed and mix thoroughly.

AMOUNT AND DIRECTIONS FOR USE

Prevention

227 mg amprolium/100 lb (5 mg/kg) body weight per day for 21 days during periods of exposure of when experience indicates that coccidiosis is likely to be a hazard.

Treatment

454 mg amprolium/100 lb (10 mg/kg) body weight per day for 5 days. Use on a herd basis only; when one or more calves show signs of coccidiosis, it is likely that the rest of the group has been exposed and all calves in the group should be treated.

The proper amount of amprolium supplement is mixed with the amount of ration usually consumed in one day. The tables below give suggested examples for using Type C medicated feed.

21 DAY PREVENTIVE PROGRAM

DMI (as % Body Weight)		4	3	2
Body Weight (lb)	Amprolium per Day (mg)	0.0125% Amprolium	0.0167% Amprolium	0.025% Amprolium
		Amount of Feed per Day in Pounds
100	227	4	3	2
200	454	8	6	4
300	681	12	9	6
400	908	16	12	8
500	1134	20	15	10
600	1361	24	18	12

5 DAY TREATMENT PROGRAM

DMI (as % Body Weight)		4	3	2
Body Weight (lb)	Amprolium per Day (mg)	0.025% Amprolium	0.033% Amprolium	0.05% Amprolium
		Amount of Feed per Day in Pounds
100	454	4	3	2
200	908	8	6	4
300	1362	12	9	6
400	1816	16	12	8
500	2268	20	15	10
600	2722	24	18	12

Bag Back Panel

PRINCIPAL DISPLAY PANEL - 22.68 kg Bag Label

INGREDIENTS AND APPEARANCE

CORID 
amprolium granule

Product Information
Product Type	OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG	Item Code (Source)	NDC: 23243-9704
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
amprolium (UNII: 95CO6N199Q) (AMPROLIUM ION - UNII:H2T307KMZR)	amprolium	250 mg  in 0.001 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 23243-9704-1	22.68 kg in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NADA	NADA012350	11/30/2017

Labeler - Huvepharma, Inc (619153559)

Registrant - Huvepharma EOOD (552691651)

Establishment
Name	Address	ID/FEI	Business Operations
Huvepharma, Inc.		883128204	medicated animal feed manufacture, analysis, pack, label, manufacture