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Draxxin IM 20 ml
Draxxin IM 20 ml
Solution for injection.
Indication(s)
Cattle: Treatment and metafylaxe of respiratory disease in cattle (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis sensitive to tulathromycine.
Treatment of infectious bovine keratoconjunctivitis (IBK) associated with Moraxella bovis sensitive to tulathromycine.
Pigs: Treatment and metafylaxe van respiratory disease in cattle in pigs (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Mycoplasma hyopneumoniae, Haemophilus parasuis and Bordetella bronchiseptica that are sensitive to tulathromycine. Draxxin should only be used when it is expected that the pigs will become ill in 2-3 days.
Route of administration and dosage
Cattle: A single subcutaneous injection of 2,5 mg tulathromycine / kg bodyweight (equivalent to 1 ml/40 kg bodyweight). For treatment of cattle over 300 kg bodyweight should be divided so that one place is not injected more than 7,5 ml.
Pigs: A single intramuscular injection of 2,5 mg tulathromycine / kg bodyweight (equivalent to 1 ml/40 kg bodyweight) in the neck.
For the treatment of pigs over 80kg bodyweight, the dose should be divided that there will be not injected more than 2ml at one place.
Nr. | 10021070 |
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Registration number | REG NL 10183 |
Brand | Zoetis |
Chilled item | No |
Active Ingredient | Tulathromycin |
Target species | Cattle, Pig, Sheep |
Legal status of supply | UDD |
Route of administration | Intramuscular Injection (IM), Subcutaneous Injection (SC) |
Withdrawal period | 0 days |
Batch | Z566809 |
Expiry date | Jun 30, 2021 |
Units per outer box | 0 |
Ingredients | Tulathromycine 100 mg/ml |