Veterinary Injection

Product Details:

COMPOSITION :

Each ml contains :

Dexamethasone Sodium Phosphate B.P.

eq. to Dexamethasone Phosphate 4 mg.

Methyl Hydroxybenzoate B.P. 0.15% w/v

(As Preservative)

Propyl Hydroxybenzoate B.P. 0.02% w/v

(As Preservative)

Water for Injection B.P. q.s.

 

INDICATIONS :

Horse, Cattle, Pigs, Dogs and Cats :

Treatment of anti-inflammatory or allergic conditions.

Cattle : Induction of parturition. Treatment of primary ketosis (acetonaemia).

Horses : Treatment of arthritis, bursitis or tenosynovitis.

 

CONTRA-INDICATIONS :

Except in Emergency Situations, Do not use in animals suffering from diabetes mellitus, Renal Insufficiency, Cardiac in sufficiency, hyperadrenocorticism or osteoporosis. Do not use in viral infections during the viraemic stage or in cases of systemic mycotic infections. 

Do not use in animals suffering from gastrointestinal or comeal ulcers or demodicosis. Do not administer Intra-articularly where there is evidence of fractures, bacterial joint infections and aseptic bone necrosis. Do not use in known cases of hypersensitivity to the active substance, to corticosteroids and to any other ingredient of the product.

 

DOSAGE AND ADMINISTRATION :

Dose according to body weight :

For the treatment of Inflammatory or allergic conditions the following average dose are advised

SPECIES       DOSAGE

Horse, Cattle, Pigs  0.06 mg/kg Body Weight

Dogs, Cats  0.1 mg/kg Body Weight

DEXACIN can be administered by Intravenous or Intramuscular injection in Horses and by Intramuscular Injection in Cattle, Pigs, Dogs and Cats.

 

WITHDRAWAL PERIOD :

Milk  : 4 days

Meat : 8 days

 

PACK SIZE :

5 ml, 30 ml, 50 ml, 100 ml Vial

COMPOSITION :
Each Vial contains :
1. Amoxicillin Sodium B.P equi. to   
Anhydrous amoxicillin 1.5 g   
Cloxacillin Sodium B.P equi. to   
Cloxacillin 1.5 g
2. Sterilised Water for Injection I.P 10 ml 1- Ampoule

INDICATIONS :
CLOX-M 3 g is indicated for the treatment of Respiratory tract infections, Brucellosis, Pyelonephritis, Hemorrhagic septicemia, Retained placenta, Black Quarter, Calf Scours. Mastitis, Metritis, Pyometra, Leptospirosis, Listeriosis, Bacterial Gastroenteritis, Dermatitis, Cystitis, Otitis and Abscesses, also it is recommended for surgical wounds and postoperative care.

DOSAGE AND ADMINISTRATION :
To prepare the Injectable solution, dissolve the contents of vial in 10 ml Sterilised water for Injection I.P.
Large animals : 7 mg/kg body weight or 1 ml of for 40-45 kg body weight (Practical Dosage) once daily for up to five days.
Administration : Intramuscular
Small animals : 15-25 mg/kg body weight once daily for up to five days.
Administration : Intramuscular
The reconstituted solution should be used immediately after preparation.
Do not allow to freeze.

WITHDRAWAL PERIOD :
Cattle       : Meat : 21 days             
  Milk  : 48 hours
Sheep & Goats : Meat : 35 days
Pig             : Meat : 14 days

PACK SIZE :
3 g in 20 ml Vial

COMPOSITION :
Each vial contains :
1. Amoxicillin Sodium B.P. equi. to   
Anhydrous amoxicillin 2 g   
Cloxacillin Sodium B.P. equi. to   
Cloxacillin 2 g
2. Sterilised Water for Injection I.P. 20 ml 1- Ampoule

INDICATIONS :
CLOX-M 4 g is indicated for the treatment of respiratory tract infections. Brucellosis, Pyelonephritis, Hemorrhagic septicemia, Retained placenta, Black Quarter, Calf Scours. Mastitis, Metritis, Pyometra, Leptospirosis, Listeriosis, Bacterial Gastroenteritis, Dermatitis, Cystitis, Otitis and Abscesses, also it is recommended for surgical wounds and postoperative care.

DOSAGE AND ADMINISTRATION :
To prepare the injectable solution, dissolve the contents of vial in 20 ml Sterile water for Injection I.P.
Large animals : 7 mg/kg body weight or 1 ml of 40-45 kg body weight (Practical Dosage) once daily for up to five days.
Administration : Intramuscular
Small animals : 15-25 mg/kg body weight once daily for up to five days.
Administration : Intramuscular
The reconstituted solution should be used immediately after preparation. 
Do not allow to freeze.

WITHDRAWAL PERIOD :
Animals must not be slaughtered and milk may not be used for human consumption during treatment.
The withdrawal periods after the last treatment are as follows:
Cattle       : Meat : 21 days       
   Milk  : 48 hours
Sheep & Goat  : Meat : 35 days
Pig       : Meat : 14 days

PACK SIZE :
4 g in 20 ml Vial

COMPOSITION :

Each ml contains :

Diminazene Aceturate 70 mg

Phenazone B.P (antipyrine) 375 mg

Water for Injection B.P q.s.

 

INDICATIONS :

Tryptansomiasis due to Trypanosoma congolense, T. Vivax and Brucei, Pyroplasmosis due to Babesia bovis, B. bigemina, B. ovis, B. motasi, B. canis, Theileriosis due to theileria annulata.

 

CONTRA-INDICATIONS :

Hypersensitivity to diminazene or phenazone.

Administration to animals with an impaired renal and/or hepatic function.

 

ADVERSE REACTIONS :

Multiple doses may cause severe nervous disturbances in dogs and camels.

 

DOSAGE AND ADMINISTRATION :

The Recommended dosage is 3.5 mg of Diminazene aceturate per kg body weight as a single Injection which is 5 ml per 100 kg body weight.

Do not exceed a total dose of 4 g of active ingredient in any animal (or 56 ml of DIMINACIN).

 

ADMINISTRATION :

Deep Intramuscular Injection.

 

WITHDRAWAL PERIOD :

Meat : 21 days

Milk  : 3 days

 

PACK SIZE :

30 ml, 100 ml Vial

COMPOSITION :

Each ml contains :

Vitamin A (as Palmitate) B.P. 2,50,000 IU

Vitamin D3 B.P. 25,000 IU

Vitamin E (dl-α-Tocopheryl Acetate) B.P. 100 IU

Benzyl Alcohol B.P. 2% V/V

Sesame Oil B.P. q.s.

 

INDICATIONS :

ELCINVIT is a well balanced combination of Vitamin A, Vitamin D3 and Vitamin E for Calves, Cattle, Goats, Sheep, Piglets, Swine, Horses, Cats and Dogs.

 

ELCINVIT is used for:

- Prevention or treatment of Vitamin A, Vitamin D3 and Vitamin E deficiencies in farm animals.

- Prevention or treatment of stress (caused by vaccination, diseases, transport, high humidity, high temperatures or extreme temperature changes).

- Improvement of feed conversion.

 

DOSAGE AND ADMINISTRATION :

For Intramuscular or Subcutaneous administration:

Cattle and Horses  : 10 ml.

Calves and Foals   : 5 ml.

Goats and Sheep  : 3 ml.

Swine    : 5 - 8 ml.

Dogs    : 1 - 5 ml.

Piglets    : 1 - 3 ml.

Cats    : 1 - 2 ml.

 

WITHDRAWAL PERIOD : 

Nil

 

PACK SIZE : 

100 ml Vial

COMPOSITION :

Each ml contains :

Flunixin meglumine USP

equi. to flunixin 50 mg

Phenol B.P. 0.5% w/v

(As Preservative)

Water for Injections B.P. q.s.

 

INDICATIONS :

Cattle : For the control of pyrexia and inflammation associated with mastitis, respiratory tract infections, endotoxemia. For the treatment of pain and inflammation associated with musculoskeletal disorders.

Horses : For the alleviation of inflammation and pain associated with musculoskeletal disorders. It is recommended for the alleviation of visceral pain associated with colic.

 

DOSAGE AND ADMINISTRATION :

Cattle : The recommended dose is 2.2 mg/kg (2 ml/45 kg) for the antipyretic effect in acute inflammatory conditions in Cattle. Intravenous administration is recommended. 

The cause of the acute inflammatory condition should be determined and appropriate concomitant therapy initiated.

Horses : The recommended dose for musculoskeletal disorders in Horses is 1.1 mg per kg (1 ml/45 kg) of bodyweight once daily. Treatment may be given by Intravenous or Intramuscular Injection and repeated for up to five days. 

Studies show that onset of activity is within two hours. Peak response occurs between 12 and 16 hours and duration of activity is 24-36 hours. The recommended dose for the alleviation of pain associated with equine colic is 1.1 mg per kg of bodyweight. 

Intravenous administration is recommended for prompt relief. Clinical studies show pain is alleviated in less than 15 minutes in many cases. Treatment may be repeated when signs of colic recur. During clinical studies approximately 10% of the Horses required one or two additional treatments. The cause of colic should be determined and treated with concomitant therapy.

 

WITHDRAWAL PERIOD :

Cattle : Meat : 7 days

   Milk  : 36 days

Horses : Meat : 7 days

All target species : 22 days

 

PACK SIZE :

50 ml, 100 ml Vial

COMPOSITION :

Each ml contains :

Methylcobalamin 500 mcg

Pyridoxine Hydrochloride B.P 50 mg

Nicotinamide B.P 50 mg

Benzyl Alcohol B.P 2% w/v

(as preservative)

Water for Injection B.P q.s.

 

Overanges of vitamins are added to compensate loss on storage.

 

INDICATIONS :

Liver disorders like fatty liver degeneration and hepatitis. Neurological disorders e.g. Nutritional Neuritis, dermatitis, macrocytic anemia.

Debility and exhaustion.

Anorexia, Fatigue.

To prevent anemia and normal RBC production.

As a supportive therapy with antimicrobials and antiparasitic treatment.

 

DOSAGE AND ADMINISTRATION :

Cattle, Buffalo, Horse : 5 to 10 ml IM or IV daily

Dog : 2 to 3 ml IM or IV daily

For normal Condition : 3 days

For Acute Condition : 7 days

 

WITHDRAWAL PERIOD :

Milk : Nil

Meat : Nil

 

PACK SIZE :

30 ml, 100 ml Vial

COMPOSITION :Each ml contains :Buparvaquone 50 mgFurosemide B.P. 55 mgSorbitan mono oleate B.P. 100 mg (as preservative)
Oil base Q.S.
INDICATIONS :For the treatment of theileriosis (east coast fever) particularly for advanced cases with pulmonary oedema. Buparvaquone kills theilerial schizonts (in lymphoid cells) and piroplasms (in red blood cells) and it supresses preschizont stages during the Incubation period of disease. Buparvaquone kill the parasite through its actions on their mitochondrial electron transport (respiratory) system. Furosemide is a diuretic, which resolves pulmonary oedema.
DOSAGE AND ADMINISTRATION :Injection by the Intramuscular route into the neck muscles at the rate of 1 ml/20 kg (2.5 mg per kg of buparvaquone and 2.75 mg/kg of furosemide).Repeat after 48 hours. In cases of exceptionally severe infections with pulmonary oedema, further treatment at half the dosage rate may be required at 24 hour interval.
WITHDRAWAL PERIOD :Milk for human consumption should not be taken from animals treated with BUPACIN PLUS until atleast 48 hours after treatment. Milk for animals treated with BUPACIN PLUS is safe for consumption by calves. Animals should not be slaughtered for human consumption until at least 42 days after treatment with BUPACIN PLUS.
WARNING / PRECAUTION :Localised swelling may occur at Injection sites but it resolves in a few days. BUPACIN PLUS is very safe so overdosage is unlikely to cause significant adverse effect. BUPACIN PLUS must be administered only by the Intramuscular route. Intravenous Injection may cause severe shock. BUPACIN PLUS is poorly mobilised after subcutaneous injection and its curative effect is greatly reduced. Furosemide is chemically similar to the sulphonamides so BUPACIN PLUS should not be used in animal with sulphonamide sensitivity.
PACK SIZE : 20 ml, 50 ml, 100 ml Vial

COMPOSITION :

Each ml contains :

Furosemide Sodium B.P.

equi. to Furosemide 50 mg.

Benzyl Alcohol B.P.1% v/v

(as preservative) 

Water for Injection B.P. q.s.

 

INDICATIONS :

It is used for treatment of congestive cardiomyopathy, pulmonary edema, hypercalcuric nephropathy, uremia and adjunctive therapy in hyperkalemia & occasionally antihypertensive agent. In cattle, it is used for the treatment of post parturient udder edema and associated structures. In race horses, it helps to prevent or to reduce epistaxis (exercise-induced pulmonary hemorrhage).

 

CONTRA-INDICATIONS :

Do not use the product in cases of acute glomerular nephritis, renal failure with anuria, electrolyte deficiency disease or overdosage with digitalis.

Do not use concurrently with aminoglycoside antibiotic treatment.

 

DOSAGE AND ADMINISTRATION :

Dogs and Cat : 1 to 2 mg/kg bodyweight once or twice daily at 6 to 8 hour intervals.

Cattle : 0.5 - 1 mg/kg bodyweight.

Horses : 0.5 - 1 mg/kg bodyweight once or twice daily at 6 to 8 hour intervals.

Administration: Intramuscular (IM) or Intravenous route (IV)

 

WITHDRAWAL PERIOD :

Do not use in horses intended for human consumption. Treated horses may never be slaughtered for human consumption.

Cattle : Meat & Milk : 48 hours.

 

PACK SIZE :

50 ml, 100 ml Vial

COMPOSITION :Each ml contains :Doramectin     10 mg/mlExcipients        q.s.
INDICATIONS :Cattle: For treatment and control of gastrointestinal nematodes, lungworms, eyeworms, warbles, lice, mange mites and ticks.Sheep: For treatment and control of gastrointestinal roundworms, mangemites and nasalbots.Pigs: For treatment of mange mites, gastrointestinal roundworms, lungworms, kidney worms and sucking lice in pigs.
DOSAGE AND ADMINISTRATION :Cattle: 1ml/50kg (200mcg/kg) bodyweight, administered in the region of the neck by subcutaneous injection.Sheep: 1ml/50kg (200mcg/kg) bodyweight, administered in the region of the neck by intramuscular injection.To treat sheep scab, a dosage of 1ml/33kg (300mcg/kg) bodyweight administered in the neck by intramuscular injection.Pigs: A single treatment of 1ml/33kg (300mcg/kg) bodyweight, administered by intramuscular injection.See datasheet for dosage for pigs<16kg
WITHDRAWAL PERIOD :Cattle :Meat and offal: 70 daysMilk: The product is not permitted for use in lactating cows used to produce milk for human cunsumption. Do not use in dry dairy cows including pregnant dairy heifers within 60 days prior to calving.Sheep:Meat and offal: 70 daysMilk:The product is not permitted for use in lactating sheep used to produce milk for human consumption.Pigs:Meat and offal: 77 days
PACK SIZE :50 ml, 100 ml Vial

COMPOSITION :

Each ml Contains :

Marbofloxacin            B.P.           100 mg
m cresol                    B.P.           2 mg
(As Preservatives)
Water for injection      B.P.           q.s.

 
INDICATIONS :
Cattle : Treatment of respiratory infections caused by sensitive strains of Pasteurella multocida, Mannheimia (Pasteurella) haemolytica and Mycoplasma bovis.
Treatment of acute mastitis caused by E. coli strains sensitive to marbofloxacin during the lactation period.
Sows : Treatment of Metritis Mastitis Agalactia Syndrome caused by bacterial strains sensitive to marbofloxacin.

 
CONTRA-INDICATIONS :
Bacterial infections with resistance to other fluoroquinolones (cross resistance). Do not administer to an animal previously found to be hypersensitive to marbofloxacin or other quinolone.

 
DOSAGE  :
Cattle : Treatment of respiratory infections: The recommended dosage is 2 mg/kg (1 ml/50kg bw) in a single daily injection by subcutaneous or intramuscular route, for 3 to 5 days.

Treatment of acute mastitis : The recommended dosage is 2 mg/kg (1 ml/50kg bw) in a single daily injection by subcutaneous or intramuscular route, for 3 consecutive days. The first injection may also be given by the intravenous route.
Sows : The recommended dosage is 2 mg/kg (1 ml/50kg bw) in a single daily injection by the intramuscular route, for 3 days.
Calves : It has been used to treat respiratory infections (bovine respiratory disease) at 2 mg/kg for 3–5 days or a single dose administered once at 8–10 mg/kg.

 
WITHDRAWAL PERIOD :
Cattle :
Meat and offals : 6 days
Milk : 36 hours
Sows :
Meat and offals : 4 days

PACK SIZE :
50 ml, 100 ml Vial