EQUISUL-SDT (Sulfadiazine/Trimethoprim)

EQUISUL-SDT
135ml - bottle
280ml - bottle
900ml - bottle
SKU : 3042135_-RX
Price: $30.95
Price: $30.95
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Veterinarian Prescription (RX) Required
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  • NEW! Oral Liquid Antibacterial for horses -- great for foals!
  • 400mg/ml (333mg sulfadiazine and 67mg of trimethoprim)
  • FDA approved product
  • As an oral sulfa antibiotic, this product works great for treating foals.
  • Similar to the previous Tribissen paste

How to Order Prescriptions

Description

    • Give at a rate of 2.7 ml or cc per 100 lbs.
    • For treatment of respiratory or other bacterial infections.
    • Don’t have to worry about getting them to eat it like the powder or tablets

Product Features

    • EQUISUL-SDT is proven effective in horses for the treatment of lower respiratory tract infections caused by susceptible strains of Streptococcus equi subsp. zooepidemicus in controlled field trials.
    • EQUISUL-SDT safety was demonstrated in a controlled study in horses at 1X, 3X and 5X the  recommended dose for 30 days.
    • Easy-to-use liquid formulation.
    • Significantly higher bioavailability on a mg-to-mg basis compared to an existing approved paste product, based on a pharmacokinetic crossover study.
    • Low incidence of side effects in our controlled safety studies.
How to Order Prescriptions

Description

    • Give at a rate of 2.7 ml or cc per 100 lbs.
    • For treatment of respiratory or other bacterial infections.
    • Don’t have to worry about getting them to eat it like the powder or tablets

Product Features

    • EQUISUL-SDT is proven effective in horses for the treatment of lower respiratory tract infections caused by susceptible strains of Streptococcus equi subsp. zooepidemicus in controlled field trials.
    • EQUISUL-SDT safety was demonstrated in a controlled study in horses at 1X, 3X and 5X the  recommended dose for 30 days.
    • Easy-to-use liquid formulation.
    • Significantly higher bioavailability on a mg-to-mg basis compared to an existing approved paste product, based on a pharmacokinetic crossover study.
    • Low incidence of side effects in our controlled safety studies.
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