AmproMed FOR CALVES description, usages, side effects, indications, overdosage, supplying and lots more!

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AmproMed FOR CALVES

Bimeda Inc., Division of Cross Vetpharm Group
Bimeda, Inc., Division of Cross Vetpharm Group




FULL PRESCRIBING INFORMATION

Uses

AmproMed™ FOR CALVES

(amprolium)

9.6% Oral Solution

Coccidiostat

FOR ORAL USE IN ANIMAL ONLY

KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN

Restricted Drug (California) – Use Only as Directed

ANADA 200-482, Approved by FDA


Net Contents:

1Gallon (128 fl oz) (3.785 L)

ACTIVE INGREDIENT: amprolium..............9.6%


INDICATIONS: An aid in the treatment and prevention of coccidiosis caused by Eimeria bovis and E. zuernii in calves. For a satisfactory diagnosis a microscopic examination of the feces should be done before treatment. When treating outbreaks, drug should be administered promptly after diagnosis is determined.

DOSAGE AND ADMINISTRATION:

USE DIRECTIONS: There are 96 mg of Amprolium in every 1 ml of AmproMed™ FOR CALVES

 5 Day Treatment Protocol  21 Day Prevention Protocol

Daily Dosage: 10 mg Amprolium/kg

(10 mg per 2.2 lb body weight)

1 fl oz = 29.57 mL

1 fl oz = 2 measuring tablespoonfuls

Daily Dosage: 5 mg Amprolium/kg

(5 mg per 2.2 lb body weight)

8 fl oz = ½ pint (236.56 mL)

16 fl oz = 1 pint (473.12 mL)

IN DRINKING WATER

Mix AmproMed™ FOR CALVES daily with fresh drinking water.

5-DAY TREATMENT: Add AMPROMED™ FOR CALVES to drinking water at the rate of 16 fl oz/100 gallon. At the usual rate of water consumption this will provide an intake of approximately 10 mg Amprolium/kg (2.2 lb) body weight. Offer this solution as the only source of water 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.

21-DAY PREVENTION: During periods of exposure or when experience indicates that coccidiosis is likely to be a hazard, add AMPROMED™ FOR CALVES to drinking water at the rate of 8 fl oz/100 gallon. At usual rates of water consumption, this will provide an intake of approximately 5 mg amprolium/kg (2.2 lb) body weight. Offer this solution as the only source of water for 21 days.


AS A DRENCH: AMPROMED™ FOR CALVES drench solutions may be stored in a clean, labeled container for up to 3 days.

5-DAY TREATMENT: Add 3 fl oz AMPROMED™ FOR CALVES to 1 pt (16 oz) of water and, with a dosage syringe, give 1 fl oz of this drench solution for each 100 lb (45 kg) body weight. This will provide a dose of approximately 10 mg amprolium/kg (2.2) body weight. Give daily 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 should be Treated.

21-DAY PREVENTION: During periods of exposure or when experience indicates that coccidiosis is likely to be a hazard, add 1 1/2 fl oz of AMPROMED™ FOR CALVES to 1 pt (16 fl oz) of water and, with a dose syringe, give 1 fl oz of this solution for each 100 lb (45 kg) body weight. This will provide a dose of approximately 5 mg amprolium/kg (2.2 lb) body weight. Give daily for 21 days.

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.

WARNING: Not for Human Use. Keep this and all drugs out of reach of children.

The Material Safety Data Sheet (MSDS) contains more detailed occupational safety information. To report adverse reaction in users, to obtain more information, or to obtain a MSDS contact Bimeda at 1-888-524-6332.

PRECAUTIONS:MAY CAUSE EYE IRRITATION. For irritation, flush with plenty of water; get medical attention. Sodium Benzoate 0.1% add as preserve.

STORAGE: Store container in an upright position. Store between 5°C - 25°C (41°F - 77°F), with brief excursions to 40°C.

AmproMed FOR  CALVES

AmproMed FOR CALVES

AMPROLIUM SOLUTION

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:61133-8251
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AMPROLIUM AMPROLIUM 96 mg

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61133-8251-3 3785 in 1 JUG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANADA ANADA200482 2012-07-30


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