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EQUIZONE

A&G Pharmaceuticals

EQUIZONE 50/100 phenylbutazone) Powder


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

INDICATIONS



EQUIZONE DOSAGE AND ADMINISTRATION





Each 10 grams of powder contains:
Phenylbutazone ............................. 1 gram
One level scoop delivers 10 grams of powder.


WARNING: Do not use in horses intended for human consumption.

HUMAN WARNINGS: Keep this and all medications out of reach of children. Dispense in tight, child resistant containers.

PRECAUTION: Concomitant use with other anti-inflammatory drugs, such as NSAIDs or corticosteroids, should be avoided or closely monitored.



Store at room temperature, 15o-30oC (59o-86oF)

Powder
For Oral Use in Horses Only



CAUTION


EQUIZONE DESCRIPTION




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INDICATIONS

Phenylbutazone is for the relief of inflammatory conditions associated with the musculoskeletal system in horses. In the treatment of inflammatory conditions associated with infections, specific anti-infective therapy should be used concurrently.

EQUIZONE DOSAGE AND ADMINISTRATION

For Horses Only: Administer orally (using the 0.6 ounce (18 mL) scoop provided) on a small amount of palatable feed and mix well. Give 1 to 2 level scoops per 500 pounds of body weight, but do not exceed 4 scoops per animal daily. Use the high dose for the first 48 hours, then gradually reduce to a maintenance dose.

EQUIZONE CONTRAINDICATIONS

Use with caution in patients who have history of drug allergy.

CLINICAL PHARMACOLOGY








HOW SUPPLIED

EQUIZONE 50 Powder is supplied in 1.1 lb (0.5 kg) jars each containing a dispensing scoop. One level scoop delivers 10 grams of powder containing 1 gram of phenylbutazone.

EQUIZONE 100 Powder is supplied in 2.2 lb (1 kg) jars each containing a dispensing scoop. One level scoop delivers 10 grams of powder containing 1 gram of phenylbutazone.

REFERENCES

















For Oral Use in Horses Only

NON-STEROIDAL ANTI-INFLAMMATORY DRUG (NSAID)

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law prohibits the extralabel use of this product in female dairy cattle 20 months of age or older.

EQUIZONE
EQUIZONE


EQUIZONE

PHEYNLBUTAZONE POWDER

Product Information

Product Type Prescription animal drug label Item Code (Source) NDC:57699-001
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHENYLBUTAZONE Phenylbutazone 1 g

Product Characteristics

Color
orange (Light orange powder)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57699-001-11 500 in 1 JAR
2 NDC:57699-001-22 1000 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANADA ANADA200334 2009-02-18


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Be sure to consult your doctor before taking any medication!
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