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Enrolen Solution for Injection is yellow – pale yellow coloured clear solution containing
enrofloxacin base 100mg per each ml
used in cattle and sheep for the treatment of respiratory, digestive and urogenital system infections caused by bacteria sensitive to enrofloxacin and also for skin and soft tissue infections additionally for secondary infections accompanied by viral infections developed by sensitive bacteria
Unless otherwise recommended by the veterinary surgeon
It is administered parenterally through subcutaneous (SC), intramuscular (IM) and intravenous (IV) routes Daily general administerd dose of enrofloxacin is 2.5mg/kg live weight
Practically applied dose: 2,5ml/100kg live weight/day
The treatment should be continued for 3-5 days
For the severe and chronic infections the administered dose should be increased to 5mg/kg
The purgation period for drug residues
The cattle and sheep should not be sent for slaughter before 10 days, respectively, following the final drug administration and during the treatment.
The cow milk produced should not be offered for human consumption during the treatment and for 4 days (8 milkings) following the final administration It should not be administered to sheep from which milk is produced for human consumption
GENERAL WARNINGS
Read package insert before using.
Consult your veterinary surgeon before using and in case an unexpected effect is observed.
Keep Enrolen away from foodstuff and out of reach of children.
Avoid purchasing and using products with damaged packages
Shelf life is 3 years as of the production date
Do not store Enrolen above 30°C
Protect from the light
Opened vials should be used within 28 days.
Keep in its carton box and comply with the usage conditions
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