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Draxxin KP
Draxxin KP
Pharmaceutical

Injection

Zoetis

Tulathromycin, Ketoprofen

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Attribute Draxxin KP
Image Draxxin KP
Trade Name Draxxin KP

دراكسين كيه بي

Product Type Pharmaceutical
Dosage Form Injection
Manufacturer Zoetis
Active Ingredients
Diseases
Package Size 50 mL, 100 mL, 250 mL, and 500 mL multi-dose glass vials
Storage Conditions Store at controlled room temperature 20°C to 25°C (68°F to 77°F). Use within 28 days of first broaching.
Dosages

Cattle

  • 2.5 mg tulathromycin and 3.0 mg ketoprofen per kg body weight (1.0 mL per 40 kg / 88 lbs) (Subcutaneous (SC)) — Single subcutaneous injection in the neck
Withdrawal Periods

Cattle

Meat: 18 days
Indications
  • Treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis.
  • Control of pyrexia (fever) associated with bovine respiratory disease in beef and non-lactating dairy cattle.
Contraindications
  • Do not use in animals with known hypersensitivity to tulathromycin, macrolides, ketoprofen, or other NSAIDs.
  • Do not use in female dairy cattle 20 months of age or older (including dry dairy cows).
  • Do not use in calves to be processed for veal.
Precautions
  • Subcutaneous injection can cause transient local tissue irritation and swelling at the injection site that may persist for up to 30 days.
  • Use with caution in animals that are dehydrated or hypovolemic, due to potential risk of renal toxicity from the NSAID component.
  • Not approved for lactating dairy cattle.
Side Effects
  • Transient pain and subcutaneous swelling at the injection site.
  • Mild gastrointestinal irritation or reduced appetite in rare instances.

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