Product Description :
TULAXINE Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass triamilide.
TULAXINE consists of an equilibrated mixture of two isomeric forms of tulathromycin in a 9:1 ratio.

Indications:
Beef and Non-Lactating Dairy Cattle
BRD – TULAXINE Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis.
and for the control of respiratory disease in cattle at high risk of developing BRD caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni,
and Mycoplasma bovis.
IBK – TULAXINE Injectable Solution is indicated for the treatment of infectious bovine keratoconjunctivitis (IBK) caused by Moraxella bovis.
Foot Rot – TULAXINE Injectable Solution is indicated for the treatment of bovine foot rot (interdigital necrobacillosis) caused by Fusobacterium necrophorum and Porphyromonas levii.
Suckling Calves, Dairy Calves, and Veal Calves
BRD – TULAXINE Injectable Solution is indicated for the treatment of BRD caused by M. haemolytica, P. multocida, H. somni, and M. bovis.
Swine
TULAXINE Injectable Solution is indicated for the treatment of swine respiratory disease (SRD) caused by Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica, Haemophilus parasuis, and Mycoplasma hyopneumoniae; and for the control of SRD caused by Actinobacillus pleuropneumoniae, Pasteurella multocida, and Mycoplasma hyopneumoniae in groups of pigs where SRD has been diagnosed.

DOSAGE:
Cattle: Inject subcutaneously as a single dose in the neck at a dosage of 2.5 mg/kg (1.1 mL/100 lb) body weight (BW) .
Do not inject more than 10 mL per injection site.
Swine: Inject intramuscularly as a single dose in the neck at a dosage of 2.5 mg/kg (0.25 mL/22lb) BW. Do not inject more than 2.5 mL per injection site.

Contraindications :
Do not use in case of hypersensitivity of the target animals to macrolide antibiotics.
Do not use simultaneously with other macrolides or lincosamides.
Do not use in lactating animals producing milk for human consumption.
Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition.

Target species:
cattle, pigs and sheep

Withdrawal periods:
Cattle (meat and offal): 22 days.
Pigs (meat and offal): 13 days.
Sheep (meat and offal): 16 days.

Presentation:
50 ml multi-dose vial, packed in single box.

Storage conditions:
Keep out of the sight and reach of children.
Store at or below 77°F (25°C) with excursions between 59-86°F (15-30°C).

Description : Procam is a non-steroidal anti-inflammatory drug (NSAID) of the oxicam class.

Indications Cattle: For use in acute respiratory infection with appropriate antibiotic therapy to reduce clinical signs in cattle. For use in diarrhea in combination with oral re-hydration therapy to reduce clinical signs in calves of over one week of age and young, non-lactating cattle. For adjunctive therapy in the treatment of acute mastitis, in combination with antibiotic therapy. For the relief of post-operative pain following dehorning in calves. Sheep: For single dose use in sheep and lambs 14 days of age or older for the alleviation of pain and inflammation. Pigs: For use in non-infectious locomotor disorders to reduce the symptoms of lameness and inflammation. For adjunctive therapy in the treatment of puerperal septicemia and toxaemia (mastitis–metritis–agalactia syndrome) with appropriate antibiotic therapy. Horses: For use in the alleviation of inflammation and relief of pain in both acute and chronic Musculo-skeletal disorders. For the relief of pain associated with equine colic.

DOSAGE AND ADMINISTRATION: Cattle: Single subcutaneous or intravenous injection of 0.5 mg meloxicam / kg body weight (ie. 2.5 ml / 100 kg body weight) in combination with antibiotic therapy or oral rehydration therapy, as appropriate. Sheep: SINGLE USE ONLY by subcutaneous injection high on the neck behind the ear. For sheep and lambs from 14 days of age 1.0 mg meloxicam/kg bodyweight (i.e. 1.0 mL/20 kg bodyweight). Pigs: A single intramuscular injection of a dose of 0.4 mg meloxicam / kg body weight (ie 2.0 ml / 100 kg body weight) in combination with appropriate antibiotic therapy. If necessary, re-administration of meloxicam can be done after 24 hours. Horses: A single intravenous injection of 0.6 mg meloxicam / kg body weight (ie 3.0 ml / 100 kg body weight). Avoid contamination during use. The plug should not be punctured more than 20 times.

Contraindications : Do not use in horses less than 6 weeks of age. Do not use in animals suffering from impaired hepatic, cardiac or renal function and hemorrhagic disorders, or where there is evidence of ulcerogenic gastrointestinal lesions. Do not use in case of hypersensitivity to the active substance or to any of the excipients. For the treatment of diarrhea in cattle, do not use in animals of less than one week of age.

Target species: Cattle, sheep, horses and pigs.

Withdrawal periods : Cattle: Meat and offal: 15 days, Milk: 5 days. Sheep: meat or offal :11 days. Pigs: Meat and offal: 5 days. Horses: Meat and offal: 5 days.

Presentation: Colorless glass injection vials of 100 mL.

Storage: Keep out of the sight and reach of children. This veterinary medicinal product does not require any special storage conditions. Shelf life after first opening the container: 28 days.

USAGE AND DOSAGE

For subcutaneous injection

Cattle – pneumonia: 1 ml per 30 kg body weight (10 mg/kg).
Cattle – interdigital necrobacillosis: 0.5 ml per 30 kg body weight (5 mg/kg).
Sheep – pneumonia and mastitis: 1 ml per 30 kg body weight (10 mg/kg).
Sheep – footrot: 0.5 ml per 30 kg body weight (5 mg/kg).

CONTRA-INDICATIONS

Administration to equine, porcine or caprine species, or to lambs weighing 15 kg or less.
Administration to cattle producing milk for human consumption.
Do not use in heifers within 60 days of calving.
Do not use together with adrenalin or β-adrenergic antagonists such as propranolol.

WITHDRAWAL TIMES

For meat: Cattle: 60 days.

Sheep: 42 days.

For milk: Sheep: 15 days.

Presentation

Multidose vials of 250 mL.

Multidose vials of 100 mL.

Storage

Store in a cool, dry place, protected from light. store among 15º to 30ºC (59°-86°F).

Keep out of reach of children and domestic animals.

Reseal after each use.

Do not smoke or eat while handling the product.

Target Species

Cattle, camels, sheep, goats and dogs.

Applied parenterally, oxytetracycline penetrates quickly into the blood and tissues, but the advanced effect of this preparation is the extremely long therapeutic effect.

Oxytetracycline acts synergistic with polymyxin.

Indicated with infections caused by microorganisms susceptible to oxytetracycline, like infections of the respiratory tract (pneumonia, bronchopneumonia), infections of the urinary tract, enteritis, (endo)metritis, mastitis, foot rot and Bedsoniasis in sheep.

Contra‑Indications:

Hypersensitivity to tetracyclines, serious kidney and/or liver disturbances, combination with penicillins or cephalosporins.

Side-effects:

Hypersensitivity reactions, irritation at injection site.

Recommendations and Warnings:

Oxytetracycline is incompatible with preparations containing polyvalent cations (Ca ++, Mg++, Fe++), because of their known interference with tetracyclines.

Do not use between 5 days before till 5 days after vaccination.

Dosage and Administration:

The general dose is 20 mg/kg body weight, (= 1 ml solution per 10 kg body weight), deep intramuscular (3 days action). Avoid application of more than 10 ml per injection site. In severe cases the injection can be repeated after 3 days. Piglets till 10 kg maximal 1 ml subcutaneous.

Withdrawal time:

21 days before slaughtering and 7 days before milking.

Storage:

Store in a cool, dry place, protected from light. Store among 15º to 30ºC (59°-86°F).

Keep out of reach of children and domestic animals.

Reseal after each use.

Target Species:

Cattle, horses, swine and dogs.

Indications

• For prevention and treatment of disease associated with parturition and puerperal tetany in cows, leaky teats, metabolic diseases of liver, anoestrus, nonspecific endometritis etc.

  As a tonic in general metabolic disorders, debility, exhaustion, repeat breeding and infertility due to phosphorus deficiency.

• For disorders of bone formation as in rickets and osteomalacia. To promote callus formation in fractures in combination with calcium and vitamin D.

• For treatment of tetany and paresis resulting from calcium, magnesium and phosphorus imbalance ( as in milk fever).

Administration and Dosage:
In acute conditions :
Large Animals : 5-20 ml. according to species and size
Small Animals : 1-3 ml.
One half of the dose should be given by intravenous route and the half by subcutaneous or intramuscular injection, divided over several sites. Injections should be repeated at short intervals until there is evidence of improvement.

In chronic conditions :
For chronic conditions, 5-10 subcutaneous or intramuscular injections should be given at 48 hour intervals with following dose rates:
Large animals : 2.5-5 ml
Small animals : 1-2 ml

Withdrawal Period

(zero) days.

Storage

Store in a cool, dry place, protected from light. Store among 15º to 30ºC.

Keep out of reach of children and domestic animals.

Reseal after each use.

Target Species

Cattle, horses, swine, camels, sheep, goats, dogs and cats.

Presentation

Multidose vials of 100 mL.

Action on the mammary gland stimulates milk let down.

Indications

Uterine inertia during parturition, postpartum bleeding, retained placenta and metritis, uterine involution after manual correction of prolapsed uterus.

Contraindications

Do not use in case of dystocia caused by abnormal presentation or foetal size or in other situations where vaginal delivery is contraindicated.

Dosage and administration

Administration by deep intramuscular injection:

Mares, cows, sows ……… 1 – 4 ml

Ewes, goats …………….. 0.2 – 1 ml

Dogs ………………………. 0.2 – 1 ml

Cats …………………….. 0.2 – 0.5 ml

Recommended dose for intravenous injection: 25% of intramuscular dose, diluted 1:10 in sterile water for injections.

Where speed of onset is not a priority, the product may be given by the subcutaneous route.

Precautions and warnings

Only administer when cervix is confirmed to be dilated, either naturally or by prior administration of oestrogens. Care should be taken to avoid accidental self-injection. Should self-injection occur, medical advice should be sought immediately. Women, particularly during lactation or the later stages of pregnancy, should avoid handling the product as it could cause smooth muscle (e.g. uterine) contraction.

Withdrawal times

None.

Storage conditions:

Store in a cool, dry place, protected from light. Store among 15º to 30ºC (59°-86°F). Do not freeze.

Keep out of reach of children and domestic animals.

Reseal after each use.

Presentation

Multidose vials of 100 mL.

Target Species

Cattle, horses, swine, camels, sheep, goats, dogs and cats.