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  • Tilmex Animal & Veterinary Products
  • Tilmex Animal & Veterinary Products

Tilmex Animal & Veterinary Products

NFA İLAÇ KİMYA SAN. TİC. LTD. ŞTİ.
  • Not Verified
  • Istanbul / Turkey
  • Established
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Description

    Explanation

TİLMEX

INJECTION SOLUTION

COMPOSITION

Each 1 ml contains 334 mg Tilmicosin Phosphate equivalent to 300 mg Tilmicosin Base.

 USAGE AREA / INDICATIONS

Cattle:

Mannheimia haemolytica and Pasteurella multocida with cattle respiratory diseases and interdigital necrobasillosis treatment.

Sheep:

Mannheimia haemolytica and Pasteurella multocida in the treatment of respiratory diseases, Dichelobacter nodosus  and  Fusobacterium necrophorum'un used in the treatment of foot caries, Staphylococcus aureus and Mycoplasma agalacticae is used in the treatment of mastitis diseases.

 

DOSAGE AND ADMINISTRATION

Unless otherwise recommended by the veterinarian;

It is administered subcutaneously only and 10 mg of tylmycosine per kg (equivalent to 1 ml per 30 kg of body weight).

Cattle:

Remove the required dose from the vial and leave the needle of the syringe in the vial. When treating animals in groups, leave the syringe in the vial and withdraw the dose to be used. After zapping, inject the animal preferably from the back of the shoulder into the base of the skin fold on the rib cage. No more than 20 ml of substance are ejected into one injection site.

Sheep:

Dosage is important according to the weight of the lambs, so the use of 2 ml syringes ensures accurate dosing. Leave the injection needle in the vial after removing the required dose from the vial. After the animal's zapping has been taken, insert the injection needle under the curled skin east into the rib cage from behind the arm and shoulder and apply the dose to the skin base. Do not apply more than 2 ml dose to each injection site. If no improvement occurs within 48 hours, re-diagnose.

Contamination of the bottle contents during use should be avoided. The bottle should be checked for any foreign matter or abnormal physical appearance, and if there is an abnormal condition, the bottle should be destroyed.

 

PHARMACEUTICAL RESIDUE PURIFICATION TIME

Cattle:

Meat: 70 days

Milk: 36 days

If medication is administered during the dry period or in the pregnant animal, the milk should not be made available to human use for 36 days.

Sheep:

Meat: 42 days

Milk: 18 days

If medication is applied to the dry animal or pregnant animal, the milk obtained should be offered to human consumption after 18 days.

 

PACKING

It is presented in cardboard boxes in 50 ml, 100 ml and 250 ml honey colored glass bottles.

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