Label: PRIBUTAZONE- phenylbutazone tablet

  • NDC Code(s): 58829-334-10
  • Packager: FIRST PRIORITY INCORPORATED
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Animal Drug Application

Drug Label Information

Updated November 16, 2023

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    For Oral Use in Horses Only.

    Non-steroidal anti-inflammatory drug (NSAID)

  • CAUTION:

    Federal law restricts this drug to use by closed when not in use. or on the order of a licensed veterinarian. Federal law prohibits the extra-label use of this product in female dairy cattle 20 months of age or older.

    Not for Use in Humans • Keep Out of Reach of Children

    Approved by FDA under ANADA # 200-433

  • DESCRIPTION & PHARMACOLOGY:

    Phenylbutazone chemically is 4-butyl-1, 2- diphenyl-3, 5-pyrazolidinedione. It has the following structural formula:

    image of phenylbute structure

    Phenylbutazone was first synthesized in 1948 and introduced into human medicine in 1949, Kuzell1,2,3, Payne4, Fleming5, and Denko6, demonstrated the clinical effectiveness of phenylbutazone in gout, gouty arthritis, acute arthritis, acute rheumatism and various other rheumatoid disorders in humans. Fabre7, Domenjoz8, Wilhelmi9, and Yourish10, have established the anti-rheumatic and anti-inflammatory activity of phenylbutazone. It is entirely unrelated to the steroid hormones.
    Toxicity of phenylbutazone has been investigated in rats and mice11, Ogilvie and Sutter12, have also made a study on the chronic toxicity of phenylbutazone in dogs. They have shown that dogs receiving 10 mg. and 100 mg. per Kg. body weight, per day for 90 days, maintain good appetites, excrete normal feces, gain weight and maintain a normal blood picture. They also report no abnormal macroscopic or microscopic changes in sacrificed animals which could have been attributed to the drug.
    Phenylbutazone has been used by Camberos13 in thoroughbred horses. Favorable results were reported in cases of traumatism, muscle rupture, strains and inflammations of the third phalanx. Results were not as favorable in the periodic treatment of osteo-arthritis of medial and distal bones of the hock, arthritis of the stifle and hip, arthrosis of the trapezious muscles, and generalized arthritis. Sutter14 reported a favorable response in chronic equine arthritis of long duration, fair results in a severely bruised mare, and poor results in two cases where the condition was limited to the third phalanx.

  • INDICATIONS:

    Phenylbutazone is for the relief of inflammatory conditions associated with the musculoskeletal system in horses.

  • DOSAGE & ADMINISTRATION:

    For horses only.
    HORSES: Orally - 1 to 2 boluses per 500 lb. body weight. Do not exceed 4 grams daily. Reduce dosage as symptoms regress. Intermittent
    treatment given only when symptoms appear may be indicated.

    image of eye clock

  • INGREDIENTS:

    Each bolus contains:
    Phenylbutazone, U.S.P. ............................. 1 gram
    Plus excipients.

  • CONTRAINDICATIONS:

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

  • PRECAUTION:

    Concomitant use with other antiinflammatory drugs, such as NSAIDS or corticosteroids, should be avoided or closely monitored. In the treatment of inflammatory conditions associated with infections, specific anti-infective therapy should be used concurrently.

  • WARNING:

    Not for use in humans. Keep out of reach of children.


    Keep Phenylbutazone Boluses in a secure location out of reach of dogs, cats, and other animals to prevent accidental ingestion or overdose.


    Do not use in horses intended for human consumption.

  • CONTACT INFORMATION:

    To report suspected adverse events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact First Priority, Inc. at (800) 650-4899 or www.prioritycare.com. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae

  • CAUTION:

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

  • AVAILABILITY:

    Available in 1 gm. boluses - 100 boluses per bottle.

    Reorder No. OM036PC

  • STORAGE:

    Store at controlled room temperature between 15°-30°C (59°-86°F). Keep container tightly closed when not in use.

    Lot No. Exp. Date

  • REFERENCES

    1. Kuzell, W.C., Schafferzick, R.W., Naughler, W.E., Gandia, G. and Mankle, E.A.: A.M.A. Arch. Inst. Med., 92; 646 (1953).
    2. Kuzell, W.C., Schafferzick, R.W., Brown, B. and Mankle, E.A.: J.A.M.A. 149; 729 (1952).
    3. Kuzell, W.C., and Schafferzick, R.W.: Calif. Med. 77; 319 (1952).
    4. Payne, R.W., Shelter, M.R., Farr, C.H., Hellbaum, A.A. and Ishmall, W.K.: J. Lab. Clin. Med., 45; 331 (1955).
    5. Fleming, J., and Will, G.: Ann. Rheumat. Dist., 12; 95 (1953).
    6. Denko, C.W., and Rumi, D.: American Pract. 6; 1865 (1956).
    7. Fabre, J., et al: Semain. Hop. (Paris) 31; 87 (1955).
    8. Domenjoz, R., et al: Arzneimittel-Forsch, 5; 488 (1955).
    9. Wilhelmi, G. and Pulver, R.: Arzneimittel- Forsch, 5; 221 (1955).
    10. Yourish, W., Paton, B., Brodie, B., Burns, J.: A.M.A. Arch. Ophth., 53; 264 (1955).
    11. Hazelton, L.W., Tusing, T.W. and Hollana, E.G.: J. Pharmacol. Exper. Ther., 109; 387 (1953).
    12. Ogilvie, F.B. and Sutter, M.D.: Vet. Med. 52; 492-4 (1957).
    13. Camberos, H.R.: Rev. Med. Vet. (Buenos Aires) 38; 9 (1956).
    14. Sutter, M.D.: Vet. Med., 53; 83 (Feb. 1958).

  • INFORMATION FOR OWNERS/CAREGIVERS

    Priority Care and Pributazone are registered trademarks of First Priority, Inc.

    Rev. 10-22

    Made in U.S.A.

    Manufactured By: FIRST PRIORITY, INC., Elgin, IL 60123

    www.prioritycare.com

    NOT RETURNABLE IF OUTDATED

  • Net Contents: 100 Boluses

    image of bottle/case label

  • INGREDIENTS AND APPEARANCE
    PRIBUTAZONE  
    phenylbutazone tablet
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:58829-334
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHENYLBUTAZONE (UNII: GN5P7K3T8S) (PHENYLBUTAZONE - UNII:GN5P7K3T8S) PHENYLBUTAZONE1 g
    Product Characteristics
    Colorwhite (WHITE) Score2 pieces
    ShapeROUND (ROUND) Size18mm
    FlavorImprint Code BUTE;1GM
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58829-334-1012 in 1 CASE
    1100 in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20043309/21/2023
    Labeler - FIRST PRIORITY INCORPORATED (179925722)
    Establishment
    NameAddressID/FEIBusiness Operations
    FIRST PRIORITY INCORPORATED179925722manufacture