Flunitrue

Flunixin injection( A New age NSAID)

Flunitrue is based on Flunixin which is a non-steroidal anti-inflammatory drug (NSAID), analgesic, and antipyretic used in horses, cattle and pigs. It targets the inflamed tissue, is mainly used for colic pain, muscle pain and joint disease, as well as to alleviate fevers and pain, and prevent endotoxemia. It is also effective in injuries of the eye.

The full analgesic and antipyretic effects usually occur 1-2 hours following treatment, but there is often an effective analgesic effect within approximately 15 minutes.

COMPOSITION

Each milliliter of FLUNIXIN INJECTION contains:

  1. Flunixin meglumine equivalent to 50 mg flunixin,
  2. 0.1 mg edetate disodium,
  3. 2.5 mg sodium formaldehyde sulfoxylate,
  4. 4.0 mg diethanolamine,
  5. 207.2 mg propylene glycol,
  6. 5.0 mg phenol as preservative,
  7. Hydrochloric acid,
  8. Water for injection q.s.

USES

Cattle:
Control of pyrexia associated with bovine respiratory disease, endotoxaemia and bovine mastitis, as well as control of inflammation in endotoxaemia. 

DOSAGE / Administration
Cattle:
The recommended dose for the control of pyrexia associated with bovine respiratory disease and endotoxaemia and the control of inflammation in endotoxaemia is 1.1 mg/kg to 2.2 mg/kg (0.5 mg to 1 mg/lb; 1 to 2 mL per 100 lbs) of bodyweight given by slow intravenous administration either once a day as a single dose or divided into two doses at 12 hour intervals for up to 3 days. The total daily dose should not exceed 2.2 mg/kg (1.0 mg/lb) of bodyweight. Avoid rapid intravenous administration of the drug.
The recommended dose rate for acute bovine mastitis is 2.2 mg/kg (1.0 mg/lb; 2mL per 100 lbs) of bodyweight given once by intravenous administration.

Withdrawal Period

Cattle:
Cattle must not be slaughtered for human consumption within 4 days of the last treatment. Milk that has been taken during treatment and for 36 hours after the last treatment must not be used for food. Not for use in dry dairy cows. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. 
Horses:
Not for use in horses intended for food.  

Contraindictions, Warnings etc

Cattle:
There are no known contraindications to this drug in cattle when used as directed. Do not use in animals showing hypersensitivity to flunixin meglumine. Use judiciously when renal impairment or gastric ulceration are suspected.inflammatory drugs should be avoided or closely monitored. Rare instances of anaphylactic-like reactions, some of which have been fatal, have been reported. See product labeling for full product information.

Pharmaceutical Precautions

Store between 2° and 30°C (36° and 86°F).

PACKING

30 ml pack size

    1. Flunixin meglumine equivalent to 50 mg flunixin
    2. 0.1 mg edetate disodium
    3. 2.5 mg sodium formaldehyde sulfoxylate
    4. 4.0 mg diethanolamine
    5. 207.2 mg propylene glycol
    6. 5.0 mg phenol as preservative
    7. Hydrochloric acid
    8. Water for injection q.s.





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