Equine (Horse) Vet Medicines

Equine (Horse) Injectable Veterinary Products

ABXOL - Ambroxol Hydrochloride Injection

COMPOSITION
Each ml contains :
Ambroxol Hydrochloride B.P  6 mg
Water For Injection B.P    q.s.
INDICATIONS
ABXOL is indicated to aid in the treatment of catarrhal inflammation of bronchi and the upper respiratory tract in Horses and Dogs.
specific indications include :
Chest Infections : acute and chronic, bronchopneumonia, catarrhal rhinitis, strangles, post-viral cough.
Uterine infections : pyometron,mucometron.
ACTION
ABXOL is a mucolytic expectorant. Ambroxol is an active metabolite of bromhexine and acts to reduce the viscosity of tenacious mucus secretions by fragmentation of long mucopolysaccharide chains,resulting in a productive cough which aids expectoration of liquefied mucoid respiratory secretions and assist in clearing and maintaining patent bronchioles and alveoli hence reducing dyspnoea. ABXOL enhances the concentrations of chemotherapeutic agents in bronchial secretions to result in a more rapid recovery.
DOSAGE AND ADMINISTRATION
Horses : 0.3 mg/kg (5ml/100kg) bodyweight twice daily.
Dogs : 0.6 mg/kg (1 ml/kg) bodyweight twice daily.
Administer ABXOL by Intravenous Injection.
WITHDRAWAL PERIOD
[Horses] : 28 Days
PACK SIZE
100 ml Vial
ABXOL
























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B-COX - Vitamin B Complex Injection

COMPOSITION
Each ml contains :
Thiamine Hydrochloride (Vitamin B1)   BP 10 mg
Riboflavin Sodium Phosphate(Vitamin B2)   BP 0.1 mg
Pyridoxine Hydrochloride (Vitamin B6)   BP 1 mg
Nicotinamide BP     10 mg
D-Panthenol USP     0.5 mg
Benzyl Alcohol BP     2% v/v
(as preservative)
Water for Injection BP   q.s.
Indication
It provides the water soluble vitamins which are essential to carbohydrate and fat metabolisum, as well as for protein synthesis.
B COMPLEX VITAMINS:
Maintains nerve functions, skin, hair and muscle tone
Are vital to all energy supply system.
Are essential to red blood cell formation.
Help Reduce the effects of stress.
It is used for supportive purposes besides principal treatment of absorption disorders, inflammatory diseases, acute an chronic infections and related recovery period during oral antibiotic and sulfonamides administration.
Dosage & Admin.
FOR IM USE ONLY
SPECIES THERAPEUTIC DOSE

Cattle, Horses   15-30 ml
Calves, Heifer   10-15 ml
Calves, Foals   5-10 ml
Sheep, Goats   5-10 ml
Swine   2-5 ml
Dogs   1-5 ml
Cats   1 ml
Withdrawal Period
Nil
Pack Size
10 ml, 30 ml, 100 ml Vial
B-COX




























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BUTACIN - Butaphosphan and Cyanocobalamin Injection

COMPOSITION
Each ml contains :
Butaphosphan   100 mg
Cyanocobalamin BP   50 mcg
Methyl Hydroxy Benzoate BP   0.1% w/v
Water for Injection BP   q.s.
INDICATIONS
BUTACIN is indicated for debilitation by acute or chronic metabolism disorders that result from poor nutrition, inadequate management or disease (e.g. developmental and nutritional disorders in young animals due to rearing disease, and (secondary) ketosis in cows). It can be used for metaphylaxis of infertility, puerperal diseases and in support of sterility treatment. It acts as a roborant in cases of stress, overexertion, exhaustion and reduced resistance and as a tonic in cases of weakness, secondary anaemia and chilling.
BUTACIN additionally supports muscular physiology, the treatment of infertility, and tetany and paresis as an adjunct to calcium and magnesium therapy.
DOSAGE AND ADMINISTRATION
In the form of Intravenous, Intramuscular and subcutaneous Injection:
Horses and cattle : 10.0 - 25.0 ml.
Foals and calves : 5.0 - 12.0 ml.
Sheep and goats : 2.5 - 8.0 ml.
Lambs : 1.5 - 2.5 ml.
Pigs : 2.5 - 10.0 ml.
Gilts : 1.0 - 2.5 ml.
Dogs : 0.5 - 5.0 ml.
Cats, fur-bearing animals : 0.5 - 2.5 ml
If necessary, repeat the treatment next day.
For birds Butacin added to the drinking water at the rate of:
Chicks and young 1.0 - 1.5 ml to 1 liter
Broilers and laying hens 2.0 - 3.0 ml to 1 liter and fed within 4 - 5 days.
WITHDRAWAL PERIOD
Meat : 0 days
Milk : 0 days
Egg : 0 days
PACK SIZE
100 ml Vial
BUTACIN































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CIT-C - Ascorbic Acid Injection

COMPOSITION
Each ml contains :
Ascorbic Acid (Vitamin C) B.P.   500.0 mg
Methyl Hydroxybenzoate B.P.   0.8 mg
(As Preservatives)
Propyl Hydroxybenzoate B.P.   0.2 mg
(As Preservatives)
Water for Injection B.P.   q.s.
Vitamin C supplement for horses and dogs.
INDICATIONS
In Cattle, Sheep, Goats, Horses, Pigs, Dogs, Cats and Poultry
- Treatment of vitamin C deficiency.
- Adjuvant therapy for asthenia, notably in cases of infection or stress.
CONTRA-INDICATIONS
Do not use in case of hypersensitivity to the active substances or any of the excipients.
DOSAGE AND ADMINISTRATION
Administer by intramuscular injection.
Horses : 5-10 mlDogs : 1-2 ml
Administer twice weekly or as directed by a veterinary surgeon.
WITHDRAWAL PERIOD
Horses Meat : 0 days
PACK SIZE
50 ml, 100 ml Vial
CIT C






















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CLOSIN 5% - Closantel Injection 5% w/v

COMPOSITION
Each ml contains :
Closantel   50 mg
Benzyl alcohol B.P   2% v/v
Propylene glycol B.P   q.s.
INDICATIONS
CLOSIN is used for the control and treatment of internal parasites including adult and juvenile liver flukes (6-8 weeks), and external parasites.
CLOSIN is indicated for the effective treatment and control of the following parasites Gastrointestinal roundworms (adult and fourth-stage larvae), Ostertagia ostertagi, O. lyrata, Haemonchus placei, Trichostongylus axei, T colubriformis, Cooperia oncophora C punctata, C pectinata, Bunostomum phlebotomum, Nematodirus helvetianus (adult only), Napathiger (adult only), Oesophagostomum radiatum.
Lungworms (adult and fourth-stage larvae) : Dictyocaulus viviparous.
Liver flukes (adult and juvenile) (6-8 weeks).
Cattle grub (parasitic stages) : Hypoderma bovis, H lineatum.
Sucking Lice : Linognathus vituli, Haematopinus eurysternus, Solenopotes capillatus.
Mange Mites (Cattle scab) : Psoroptes ovis, Sarcoptes scabiei var. bovis.
DOSAGE AND ADMINISTRATION
2 ml/50 kg of bodyweight by Subcutaneous Injection only
WITHDRAWAL PERIOD
Meat: 49 days
PACK SIZE
100 ml vial
CLOSIN 5%






















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CLOSIN 10% - Closantel Injection 10% w/v

COMPOSITION
Each ml contains :
Closantel   100 mg
Benzyl alcohol B.P   4 % v/v
Propylene glycol B.P   q.s.
INDICATIONS
CLOSIN 10 % is used for the control and treatment of internal parasites including adult and juvenile liver flukes (6-8 weeks), and external parasites.
CLOSIN 10 % is indicated for the effective treatment and control of the following parasites - Gastrointestinal roundworms (adult and fourth-stage larvae), Ostertagia ostertagi, O. lyrata, Haemonchus placei, Trichostongylus axei, T colubriformis, Cooperia oncophora C punctata, C pectinata, Bunostomum phlebotomum, Nematodirus helvetianus (adult only), Napathiger (adult only), Oesophagostomum radiatum.
Lungworms (adult and fourth-stage larvae): Dictyocaulus viviparous.
Liver flukes (adult and juvenile) (6-8 weeks).
Cattle grub (parasitic stages): Hypoderma bovis, H lineatum.
Sucking Lice: Linognathus vituli, Haematopinus eurysternus, Solenopotes capillatus.
Mange Mites (Cattle scab): Psoroptes ovis, Sarcoptes scabiei var. bovis.
DOSAGE AND ADMINISTRATION
Cattle , Sheep :
1ml / 50kg of bodyweight by Subcutaneous Injection only
WITHDRAWAL PERIOD
Meat: 49 days
PACK SIZE
50 ml, 100 ml Vial
CLOSIN 10%






















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CLOX-M 3 g. - Amoxicillin & Cloxacillin Powder For Injection 3 g

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
CLOTIN FORTE




























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CLOX-M 4 g. - Amoxicillin & Cloxacillin Powder For Injection 4 g

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
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COMIN - Cyanocobalamin Injection

COMPOSITION
Each ml contains :
Cyanocobalamin B.P    500 mcg
Benzyl alcohol B.P     1.5% v/v
Water For Injection B.P   q.s.
ACTION
Vitamin B12 is essential B complex vitamins, vitally involved in many critical metabolic processes related to coenzymes for tissue formation,DNA synthesis, complete utillisation of carbohydrates and proteins for nervous tissue maintenance and energy production, and blood counts. Vitamin B12 acts in synergy in the formulation of DNA, and deficiencies can have serious consequences, both in performance Horses with a high tissue turnover rate,and in pregnancy and growth of young foals.Clinically the first sign of deficiency is anaemia. Lack of Vitamin B12 can create anaemias. As the deficiency may be indistinguishable for either of these essential vitamins, they are often grouped in one product for therapeutic and preventive use. Vitamin B12 is an essential B group vitamin which is involved in many metabolic processes as an important coenzyme. Its most important role is in the formation of nucleic acids(DNA) from amino acids. Vitamin B12 is vital to the formation of red and white blood cells and haemoglobin, as well as for rapidly dividing cells which include gastrointestinal epithelial cells, the growing foetus, skin and hair.
DOSAGE AND ADMINISTRATION
Horses : 5-10 ml
Dogs : 1-2 ml
Administer by Intramuscular Injection regularly twice weekly advised by a Veterinary surgeon.
WITHDRAWAL PERIOD
[Horses] : Nil
PACK SIZE
100 ml Vial
COMIN































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CRAMINE - Chlorphenamine Injection B.P. 10 mg/ml

COMPOSITION
Each ml contains :
Chlorphenamine Maleate B.P. 10 mg.
Phenylmercuric Nitrate B.P. 0.002% w/v.
(As Preservative)
Water for Injection B.P. q.s.
INDICATIONS
1. Allergic reactions and allergic disorders with manifestation of acute respiratory signs.
2. Rhinitis, dyspnoea, pulmonary emphysema, pulmonary oedema, asthama and hay fever.
3. Eczema, dermatitis, urticaria, insect bite, tail eczema in Horses, toxic hoof corns.
4. Ruminal atony, tympany and bloat in ruminants.
5. Puerperal toxaemia and secondary placental retention, acute septic metritis and gangrenous mastitis.
6. Reactions and other drug allergies and anaphylactic shock.
CONTRA-INDICATIONS
Do not use in animals known to be hypersensitive to chlorphenamine.
Do not use in rental and hepatic insufficiency.
DOSAGE AND ADMINISTRATION
Cattle & Horse : 5-10 ml
Sheep & Goat : 0.5 - 2 ml. By Intramuscular route.
Canine : 0.5 - 2 ml
Poultry : 0.5 - 1 ml. By Intramuscular route.
Or as directed by Physician.
WITHDRAWAL PERIOD
Nil
PACK SIZE
30ml, 100 ml Vial
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CULANATE - Calcium Levulinate, Vitamin D3 & Vitamin B12 Injection

COMPOSITION
Each ml contains : Calcium Levulinate USP   76.4 mg (equi.to 10 mg of lonic Calcium) *Cholecalciferol (Vit. D3) B.P.   5000 IU *Cyanocobalamin (Vit. D12) B.P.   50 mcg Benzyl alcohol B.P.   1.5% v/v [Preservative] Water for Injection B.P.   q.s. *Required overages are added.
INDICATIONS
Prevention and treatment of hypocalcaemia, debility, weakness. To improve health productivity and milk yield.
DOSAGE AND ADMINISTRATION
For Intramuscular use only: Cattle and Buffalo (Prepartum) 5-10 ml/head/twice a/week Cattle and Buffalo (postpartum) 10-15 ml/head/twice a/week Cattle and Buffalo (for other condition) 10 ml thrice/week Small animals 1-5 ml thrice/week Or as directed by Veterinarian.
WITHDRAWAL PERIOD
Milk : Nil
Meat : Nil
PACK SIZE
100 ml Vial
CULANATE


























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DEXACIN VET - Dexamethasone Sodium Phosphate Injection B.P. 4 mg/ml

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































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DEXACIN-F - Dexamethasone with Furosemide Injection

COMPOSITION
Each ml contains :
Furosemide B.P             20 mg
Dexamethasone Sodium Phosphate B.P  0.63 mg
Phenol B.P               0.5% v/v
Water for Injection B.P          q.s.
INDICATIONS
For treatment of edemas of different etiology in Bovines, Sheep and Horses. Especially indicated for treatment of post partum udder edema in Cows.
ADMINISTRATION ROUTE AND DOSAGE
Administer by intramuscular or subcutaneous route, at 0.5 ml per 20 kg of body weight. Dose can be repeated after 24 hr.
Duration of treatment may vary according to each clinical case; usually 2 doses with a 24 hr interval are sufficient.
WITHDRAWAL PERIOD
Meat & Offals : 3 days
Milk : 2 days
PACK SIZE
50 ml, 100 ml Vial
DEXACIN-F































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DEXAZIDE - Dexamethasone with Hydrochlorothiazide Injection

COMPOSITION
Each ml contains :
Dexamethasone sodium phosphate B.P   0.50 mg
Hydrochlorothiazide B.P          50.00 mg
Propylene glycol B.P            0.15 ml
Benzyl alcohol B.P              0.01 ml
Water for Injection B.P            q.s.
INDICATIONS
CATTLE :
  • Congestion and oedema of the udder.
  • Early persistant lactation edema.
  • Pulmonary congestion and edema.
  • Edematous infiltration of surgical wounds.
  • Edema in allergic conditions.

HORSES :
  • Generalised congestion and oedema
  • Oedema of sheath Anasarca
  • Oedema in allergic conditions

ADMINISTRATION ROUTE AND DOSAGE
Dexazide injection may be administered by Intravenous, intramuscular, subcutaneous injection.
Cattle and ault Horses :
Preventative treatment : 10 ml daily for 3 days.
Curative treatment :
Congestion and mild oedema : 10 ml daily for 2 or 3 days
Congestion and severe oedema : 20 ml daily for 2 days and 10 ml the third day.
Foals - Calves : 2 ml per 40 - 50 kg bodyweight daily for 3 days
WITHDRAWAL PERIOD
Cattle : Meat and offal : 28 days
Milk : 7 days
Treated Horses may never be slaughtered for human consumption.
PACK SIZE
50 ml, 100 ml Vial
DEXAZIDE































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DIMINACIN R.T.U. - Diminazene Aceturate 7% Injection

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.
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
30ml, 100 ml Vial
DIMINACIN R.T.U.






















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DRAMINE - Diphenhydramine (Antihistamine) - Vitamin B & C Injection

COMPOSITION
Each ml contains :
Diphenhydramine hydrochloride  6.25 mg
Thaimine HCL (vit. B1)       20 mg
Ascorbic acid (vit C)        112.4 mg
Glucose              100 mg
Water for Injection B.P      q.s.
INDICATIONS
Cattle : Acidosis of the rumen, necrosis of the cerebral cortex, disturbances of the central nervous system and the metabolism. Also in blood milking.
Pigs : Especially oedema disease, gastric ulcer, Pruritus and all disturbances of metabolism.
Dogs & Cats : Allergies, diseases of the skin, especially in conjunction with itch.
DOSAGE AND ADMINISTRATION
DRAMINE can be administered Subcutaneously, Intramuscularly or Intravenosly.
Dogs & Cats : 1 to 5 ml
Sheep & Goats : 5 to 10 ml
Calf & Pigs : 5 to 10 ml
Cattle & Horses : 20 to 50 ml
WITHDRAWAL PERIOD
Meat & Milk : 5 days.
PACK SIZE
100 ml Vial
DRAMINE

























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FLUXANE - Flunixin Meglumine Injection 5% w/v

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 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 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
FLUXANE


























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FUTIC - Furosemide Injection BP 5% w/v

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 as antihypertensive agent. In Cattle it is used for the treatment of post parturient udder edema & associated structures. In race Horses, it helps to prevent or to reduce epistaxis.(exercise included 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 or Intravenous route
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
FUTIC






















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I-CARE - Levocarnitine Injection

COMPOSITION
Each ml contains :
Levocarnitine B.P     200 mg
Water For Injection B.P   q.s.
INDICATIONS
To improve both sprint and endurance performance.
ACTION
  • Muscle levels of Levocarnitine determine the exercise capacity of muscles.
  • Levocarnitine forms the essential transport system for use of fats as an energy source.
  • Levocarnitine may help delay muscle fatigue and improve endurance.
  • Levocarnitine is essential for normal heart function.
  • Performance Horses recover more effeciently when supplemented with Levocarnitine.

Levocarnitine is an amino acid which helps transport fats into muscle cells. Levocarnitine is essential in the transport of fats into muscle cells for production. The muscle levels of Levocarnitine determine the exercise capacity of muscles. By using fats as energy for muscle contractions, the body is glycogen and delaying the accumulation of lactic acid. Levocarnitine delays muscle fatigue by reducing lactic acid formation and improves performance and endurance. Levocarnitine forms an essential part of the transport system which moves fatty acids into the mitochondria (cell furnaces) for energy production. It thus acts as a buffer by inhibiting lactic acid buildup in muscles, helping to delay fatigue and prevent Tying Up. Demand for Levocarnitine in heavily exercising Horses is often not met from the diet, as large amounts are consumed during exercise. Supplementing with Levocarnitine results improved energy supply, increased use of fatty acids as an energy source, decreased lactate buildup and a significant increase in maximum work output.

DOSAGE AND ADMINISTRATION
Injection: Horses: 3 ml per 100 kg bodyweight ( 15 ml per average horse) by Intravenous or Intramuscular Injection 2-3 times weekly.
Dogs.1 ml/10 kg bodyweight.
Administer 2-3 time weekly or as directed by veterinary surgeon
WITHDRAWAL PERIOD
[Horses] : Nil
PACK SIZE
100 ml Vial
I-CARE




























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I-CLOR - Dichloro Acetic Acid Injection

COMPOSITION
Each ml contains :
Dichloro-acetic acid    120 mcg
Sodium gluconate USP  250 mg
Water For Injection BP  q.s.
INDICATIONS
To help reduce the incidence of Tying Up by reducing the build-up of lactic acid in muscle cells.
ACTION
I-CLOR contains dichloroacetic acid, which is an activator of the enzyme pyruvate dehydrogenase. This enzyme plays a central role in the process of lactic acid production during hard work.
Supplementation with dichloroacetic acid (I-CLOR) results in activation of the enzyme pyruvate dehydrogenase, leading to a reduction in the rate of lactic levels results in a reduction in pH which contributes to muscle fatigue and decreased muscle performance. Supplementation with I-CLOR has been shown to reduce lactic acid accumulation during exercise, and produce a significant delay in muscle fatigue. The pathogenesis of Exertional Rhabdomyolysis(”Tying Up”) in Horses is related to lactic acidosis during exercise, and associated low muscle pH. Sodium bicarbonate and dimethylglycine (DMG), which may help to reduce lactic acid accumulation during exercise, have been used to assist in the prevention of Tying Up in horses. Similarly, I-CLOR results in a reduction in the rate of lactate accumulation, and a delay in the onset of muscle fatigue.
DOSAGE AND ADMINISTRATION
Give 20 - 40 ml by Intravenous Injection(diluted in 1 Litre saline or administer via catheter). Administer once weekly for 4 weeks then discontinue for 4 weeks before repeating the course.
WITHDRAWAL PERIOD
[Horses] : Nil
PACK SIZE
100 ml Vial
I-CLOR

























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I-LIC - Folic Acid Injection

COMPOSITION
Each ml contains :
Folic acid B.P       15 mg
Water For Injections B.P  q.s.
ACTION
Folic Acid is essential B complex vitamins, vitally involved in many critical metabolic processes related to conenzymes for tissue formation, DNA synthesis, complete utillisation of carbohydrates and proteins for nervous tissue maintainance and energy production and blood counts. Folic Acid acts in synergy in the formulation of DNA, and deficiencies can have serious consequences, both in performance Horses with a high tissue turnover rate and in pregnancy and growth of young foals. Clinically the first sign of deficiency is anaemia. Lack of either folic Acid can create anaemias. As the deficiency may be indistinguishable for either of these essential vitamins, they are often grouped in one product for therapeutic and preventive use. Folic Acid is an essential B group vitamin which is involved in many metabolic processes as an important coenzyme. Its most important role is in the formation of nucleic acids(DNA) from amino acids. Folic Acid is vital to the formation of red and white blood cells and haemoglobin, as well as for rapidly dividing cells which include gastrointestinal epitheleal cells, the growing foetus, skin and hair. Folic Acid is involved in the formation of the amino acids methionine and glycine, as well as the vitamin choline. Folic Acid supplementation is highly recommended during pregnancy, as deficiencies in young growing animals are often associated with retardation. Cooking and storage of feeds destroy Folic Acid levels. When antibiotics, particularly sulphur drugs are used for extended periods, the normal synthesis of folic acid in the gut will be reduced and the requirement for folic acid are increased. Supplements of folic acid are reported to improve antibody respective animal.
DOSAGE AND ADMINISTRATION
Horses : 5 - 10 ml
Dogs : 1 - 2 ml
Administer by Intramuscular Injection regularly twice weekly advised by a Veterinary surgeon.
WITHDRAWAL PERIOD
[Horses] : Nil
PACK SIZE
100 ml Vial
I-LIC































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IMIX - Imidocarb Dipropionate Aqueous Injection Solution

COMPOSITION
Each ml contains :
Imidocarb Dipropionate   120 mg
Benzyl Alcohol B.P     2.0% w/v
Water For Injections B.P   q.s.
INDICATIONS
IMIX is used for the treatment of babesiosis in Cattle, Sheep, Horses and Dogs and of anaplasmosis in Cattle. IMIX will also treat ehrlichiosis in Dogs. For Subcutaneous or Intramuscular Injection.
DOSAGE AND ADMINISTRATION
Dose according to body weight:
Cattle : 1 ml per 100 kg bodyweight. In treating mixed infections due to Anaplasma and Babesia, administer 2.5 ml per 100 kg body weight.
Sheep : 0.5 ml per 50 kg bodyweight.
Horses : 2 ml per 100 kg bodyweight. (Intramuscular injection is preferred). In most cases, a single dose will effect a complete cure, but treatment of B. equi infections in Horses may require 2 doses at an interval of 24 hours.
Dogs : 0.25 ml per 10 kg body weight. In treating mixed infection due to Ehrlichina and Babesia, administer 0.5 ml per 10 kg bodyweight, 2 doses at an interval of 14 days.
It is advised to screen the blood after one treatment for presence of the parasite. Repeat treatment for presence of the parasite. Repeat treatment if the test is positive.
WITHDRAWAL PERIOD
Meat : 28 days
Milk : 7 days.
PACK SIZE
20 ml, 50 ml, 100 ml Vial
IMIX






















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IMOLY 5% - Oxytetracycline Hydrochloride Injection 5%

COMPOSITION
Each ml contains :
Oxytetracycline Hydrochloride B.P  50 mg
Propylene Glycol B.P        q.s.
INDICATIONS
The treatment of infections caused by organisms sensitive to oxytetracycline in Horses, Cattle, Camel, Sheep, Goat, Dogs and Cats. In vitro, Oxytetracycline is active against a range of both Gram-positive and Gram-negative microorganisms including Staphyicocccus spp., Listeria monocytogenes, Mannheimia haemolytica, Haemophilus parahaemolyticus, Bordetella bronchiseptica, and against Chlamydophila abortus (Formerly Chlamydia pasittaci), the causative organism of enzootic abortion in Sheep.
CONTRA-INDICATIONS
Do not administer to Horses during concomitant therapy with corticosteroids.
A transient swelling may be observed following Intramuscular administration in Horses and Subcutaneous administration in Dogs.
The use of tetracyclines during the period of tooth and bone development, including late pregnancy, may lead to discolouration.
Not to be used in Sheep producing milk for human consumption.
Not to be used in Horses intended for human consumption.
DOSAGE AND ADMINISTRATION
Large Animal : 5-10 mg Oxyteracycline per Kg Body Weight for 3 to 5 days by IM , IV or SC Injection
Small Animal : 5-10 mg Oxyteracycline per Kg Body Weight for 3 to 5 days by IM or IV Injection
WITHDRAWAL PERIOD
Animal must not be slaughtered and milk should not be used for human consumption during treatment.
The withdrawal periods after the last treatment for Cattle, Sheep are :
Cattle : Milk : 6 days Meat : 35 days
Sheep : Meat : 14 days
PACK SIZE
50 ml, 100 ml Vial
IMOLY 5%




























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IMOLY 10% - Oxytetracycline Injection 10%

COMPOSITION
Each ml contains :
Oxytetracycline Dihydrate B.P eq. to
Anhydrous Oxytetracycline  100 mg
Propylene Glyco B.P     q.s.
INDICATIONS
The treatment of infections caused by organisms sensitive to oxytetracycline in Horses, Cattle, Camel, Sheep, Goat, Dogs and Cats. In vitro, Oxytetracycline is active against a range of both Gram-positive and Gram-negative microorganisms including Staphylcocccus spp., Listeria monocytogenes, Mannheimia haemolytica, Haemophilus parahaemolyticus, Bordetella bronchiseptica, and against Chlamydophila abortus (Formerly Chlamydia psittaci), the causative organism of enzootic abortion in Sheep.
CONTRA-INDICATIONS
Do not administer to Horses during concomitant therapy with corticosteroids.
A transient swelling may be observed following Intramuscular administration in Horses and Subcutaneous administration in Dogs. The use of tetracyclines during the period of tooth and bone development, including late pregnancy, may lead to discolouration. Photodermatitis may occur after treatment if exposure to intense sunlight.
Not for Intravenous administration in Dogs or Cats. It is not recommended to administer bacteriostatic and bactericidal antimicrobials concurrently.
DOSAGE AND ADMINISTRATION
For Intramuscular or Subcutaneous administration:
Full-grown animals : 1 ml per 10 - 20 kg body weight for 3 - 5 days.
Young animals : 2 ml per 10 - 20 kg body weight for 3 - 5 days.
Do not administer more than 20 ml in Cattle, more than 10 ml in Swine and more than 5 ml in Calves, Goats and Sheep per Injection site.
WITHDRAWAL PERIOD
Animal must not be slaughtered and milk should not be used for human consumption during treatment.
The withdrawal periods after the last treatment for Cattle, Sheep, Camel, Goat are :
Cattle & Camel : Milk : 6 days Meat : 35 days
Sheep & Goat : Meat : 14 days
PACK SIZE
50 ml, 100 ml Vial
IMOLY 10%

























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IMOLY 20% LA - Oxytetracycline Injection Long Acting 20%

COMPOSITION
Each ml contains :
Oxytetracycline Dihydrate B.P
eq. to Anhydrous Oxytetracycline  200 mg
in 2-Pyrrolidone Vehicle system  q.s.
INDICATIONS
IMOLY 20% is indicated in the treatment and control of disease in Cattle, Sheep and Pigs caused by or associated with organisms sensitive to Oxytetracycline.
For the treatment and control of pasteurellosis and pneumonia caused by oxytetracycline sensitive organisms and as an aid in the treatment of infectious bovine keratoconjunctivitis (New Forest Disease) due to oxytetracycline sensitive strains of Moraxeila bovis. This product may also be of value for foul-in-the-foot.
CONTRA-INDICATIONS
Not recommended for Cats, Dogs, Horses and Donkeys.
The use of this product during the period of tooth development including late pregnancy may lead to tooth discoloration.
DOSAGE AND ADMINISTRATION
For Intramuscular or Subcutaneous administration:
General : 1 ml per 10 kg body weight.
This dosage can be repeated after 48 hours when necessary.
Do not administer more than 20 ml in Cattle, more than 10 ml in Swine and more than 5 ml in Calves, Goats and Sheep per Injection site.
WITHDRAWAL PERIOD
Milk for human consumption should not be taken during treatment. Milk intended for human consumption may be taken only after 7 days from the last treatment. Not for use in ewes producing milk for human consumption. Animals may only be slaughtered for human consumption after last treatment, according to the below table.
Species      Meat withdrawal periods
Cattle & Sheep   28 days
Pigs        35 days
PACK SIZE
20 ml, 50 ml, 100 ml Vial
IMOLY 20% LA




























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IMOLY 30% LA - Oxytetracycline Injection Long Acting 30%

COMPOSITION
Each ml contains :
Oxytetracycline Dihydrate B.P
eq. to Anhydrous Oxytetracycline  300 mg
in 2-Pyrrolidone Vehicle system  q.s.
INDICATIONS
IMOLY 30% is indicated in the treatment and control of disease in Cattle, Sheep and Pigs caused by, or associated with, organisms sensitive to Oxytetracycline.
Cattle : For the treatment and control of pasteurellosis and pneumonia caused by Oxytetracycline sensitive organisms and as an aid in the treatment of infectious bovine keratoconjunctivitis (New Forest Disease) due to Oxytetracycline sensitive strains of Moraxeila bovis. This product may also be of value for foul-in-the-foot.
Pigs : For the treatment of pneumonia caused by Pasteurella.
Sheep : For the control of enzootic abortion and pneumonia caused by Oxytetracyclinesensitive organisms. This product may be used as an aid in the treatment of foot rot, acute, severe mastitis and infectious ovine keratoconjuctivitis (pink-eye).
CONTRA-INDICATIONS
Not recommended for Cats, Dogs, Horses and Donkeys.
The use of this product during the period of tooth development including late pregnancy may lead to tooth discoloration.
DOSAGE AND ADMINISTRATION
I.M./Subcutaneous use
Deep intramuscular use only in large & small animals and subcutaneous in poultry.
In large & small animal & poultry.
1ml / 10kg body wt.
0.25ml / 1kg body wt.
WITHDRAWAL PERIOD
For meat (standard dose):
Cattle and sheep : 28 days.
Swine : 14 days.
For meat (high dose):
Cattle : 35 days.
Sheep and swine : 28 days.
For milk :
Cattle : 10 days.
Sheep : 8 days.
PACK SIZE
20 ml, 50 ml, 100 ml Vial
IMOLY 30%





































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INCEFT - Ceftiofur Sodium Powder For Injection

COMPOSITION
Each vial contains :
Ceftiofur Sodium eq. to Ceftiofur  1 g

For Intramuscular Injection in Cattle, Buffaloes, Sheep & Goat. It can be used in lactating dairy animals.
INDICATIONS
  • Genital infections of bovine (acute metritis, cervicitis, prolapsed related to retention of placenta cases) associated with Arcanobacterium pyogenes, Fusobacterium necrophorum and bacteroids spp.

  • Respiratory diseases of Cattle, Buffalo, Sheep and Goat (Shipping fever, pneumonia) associated with Pasteurella haemolytica, Pasteurella multocida & Haemophilussomnus.

  • Acute interdigital necrobacillosis (foot rot, pododermatitis) caused by Fusobacterium and Bacteroides.
DOSAGE AND ADMINISTRATION
Cattle, Sheep and Goat : 1.1 to 2.2 mg/kg b.wt. or 1 to 2 ml (after reconstitution) /45.45 kg b.wt. by IM use only, once daily for 3-5 days.
Buffalo : 2 to 2.4 mg/kg b.wt. by IM use only, once daily for 3-5 days.
Dog : 2.2 mg/kg b.wt. by SC use only, once daily for 5 to 14 days.
Camel : 2.2 mg/kg b.wt. by IM once daily for 3-5 days.
Horse : 2.2 to 4.4 mg/kg b.wt. or 1 to 2 ml (after reconstitution) /22.72 kg b.wt. by IM use only. once daily for 3 to 5 days.
Swine : 3 to 5 mg/kg b.wt. or 1 to 1.7 ml (after reconstitution) / 16.66 kg b.wt. by IM use only, once daily for 3 to 5 days.
Chicken (day-old chick) : 0.08 to 0.2 mg/Chick, SC use only in the neck region (1 g vial after reconstitution with 20 ml water for injection will treat approximately 5,000 to 12,500 day-old chicks)
WITHDRAWAL PERIOD
For Cattle, Buffalo & Swine :
Milk : Nil | Meat : 4 days

For Sheep & Goat :
Milk : Nil | Meat: Nil
PACK SIZE
1 g in 30 ml Vial
INCEFT




























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IROFLOX SA - Enrofloxacin Injection

COMPOSITION
Each ml contains :
Enrofloxacin USP     100 mg
Benzyl Alcohol B.P    1.5% v/v
[as preservative]
Water for Injection B.P   q.s.
INDICATIONS
Shipping fever pneumonia (H.S), Pnemonia, Pleuropneumonia, Pseudorinderpest and Urinary infections, mastitis caused by mycoplasma spp. Respiratory and enteric diseases (Pasteurellosis, Mycoplasmosis, Colibacillosis, Colisepticaemia and secondary bacterial complication during viral infections).
Mastitis caused by susceptible microorganisms and renal infection.
IROFLOX SA is effective against the following microorganism : Mycoplasma spp., E.coli, Salmonella spp., Haemophilus spp., Pasteurella spp., Klebsiella spp., Proteus spp., Vibrio parahaemolyticus and Staphylococcus aureus.
DOSAGE AND ADMINISTRATION
Cattle, Buffaloes, Sheep, Goats and Camels:
As directed by the veterinarian. OR 1 ml per 20-40 kg body weight depending upon the severity of injection. (2.5-5 mg of Enrofloxacin 1kg body weight) the second administration should be administered after 72 hours, if required.
ROUTE :
For I.M./SC/Slow I.V. Use.
WITHDRAWAL PERIOD
Animals must not be slaughtered and milk should not be used for human consumption during treatment.
The withdrawal periods after the last traetment are:
Cattle:
For Intravenous route : Meat : 4 days
Milk : 72 hours
For Subcutaneous route : Meat : 14 days
Milk : 84 hours
PACK SIZE
15 ml, 100 ml Vial
IROFLOX SA




























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K-GEN 10% - Gentamicin Injection BP

COMPOSITION
Each ml contains :
Gentamicin Sulphate B.P
eq. to Gentamicin Base     100 mg
Methyl Hydroxybenzoate B.P  0.18% w/v
(As Preservative)
Propyl Hydroxybenzoate B.P  0.02% w/v
(As Preservative)
Water for Injection B.P     q.s.
INDICATIONS
Gastrointestinal, respiratory infections, arthritis, poly-arthritis, meningitis, mastitis & metritis caused by Gentamicin sensitive bacteria, like E.Coli, Pasteurella, Klebsiella and salmonella spp., in Calves, Cattle, Horse, Goats and Sheep.
DOSAGE AND ADMINISTRATION
For Intramuscular administration:
General: Twice daily 1 ml per 20 - 40 kg body weight for 3 days.
WITHDRAWAL PERIOD
- For kidneys : 45 days.
- For meat : 7 days.
- For milk : 3 days.
PACK SIZE
100 ml Vial
K-GEN






















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MELOXIN-I - Meloxicam Injection 5 mg/ml

COMPOSITION
Each ml contains :
Meloxicam B.P            5 mg
Benzyl alcohol (as preservative) B.P  2% v/v
Water for Injection B.P        q.s.
INDICATIONS
Respiratory inflammations
  • Pneumonia
  • Broncho-Pneumonia
  • Pleuritis
Inflammation of Musculoskeletal System
  • Arthritis
  • Synovitis
  • Myositis
  • Tendonitis
  • Laminitis
  • Bursitis
Gynaecological Inflammatory Conditions
  • Metritis
  • Prolapse of uterus
Other Indications
  • Mastitis
  • Otitis
  • Pharyngitis
  • Postoperative Pain
  • Pyrexia of Unknown Origin
  • Pain and fever associated with inflammation
DOSAGE AND ADMINISTRATION
Cow, Buffalo, Horse, Sheep & Goat :
1ml / 10kg (Respiratory Inflammation & Prolapse)
1ml / 25kg (Other Indications)
Dog : 1ml / 10 kg
WITHDRAWAL PERIOD
Cattle :
Meat and offal : 15 days
Milk : 5 days
Horses & Swine :
Meat and offal : 5 days
PACK SIZE
30 ml, 100 ml Vial
MELOXIN-I

















































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MELOXIN-20 - Meloxicam Injection 20 mg/ml

COMPOSITION
Each ml contains :
Meloxicam B.P     20 mg
Benzyl alcohol B.P    2% v/v
Water for Injection B.P  q.s.
INDICATIONS
Meloxin-20 Injection is indicated for anti-inflammatory & anti-pyretic purpose and the alleviation of pain in Cattle.
CONTRA-INDICATIONS
Do not use in animals suffering from impaired hepatic, cardiac or renal function and haemorrhagic 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 diarrhoea in Cattle, do not use in animals of less than one week of age.
DOSAGE AND ADMINISTRATION
Cattle : Administer with a dose 2.5 ml / 100 kg body weight with IM.

WITHDRAWAL PERIOD
Cattle :
Meat : 15 days
Milk : 5 days
PACK SIZE
100 ml Vial
MELOXIN-20






















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MICIX - Amikacin Injection 250 mg/ml

COMPOSITION
Each ml contains :
Amikacin Sulphate B.P
Equivalent to Amikacin base  250 mg
Methyl hydroxy benzoate B.P  0.18% w/v
Propyl Hydroxy benzoate B.P  0.025% w/v
Water for Injection B.P     q.s.
INDICATIONS
Amikacin is used clinically to treat serious gram negative infections in most species. It is often used in settings where gentamicin-resistant bacteria are a clinical problem. The inherent toxicity of the aminoglycosides limit their systemic use to serious infections when there is either a documented lack of susceptibility to other less toxic antibiotics or when the clinical situation dictates immediate treatment of a presumed gram negative infection before culture and susceptibility results are reported. Amikacin is also approved for Intrauterine infusion in mares.
CONTRA-INDICATIONS
Aminoglycosides are contraindicated in patients who are hypersensitive to them. Because these drugs are often the only effective agents in severe gramnegative infections there are no other absolute contraindications to their use. However, they should be used with extreme caution in patients with preexisting renal disease with concomitant monitoring and dosage interval adjustments made. Other risk factors for the development of toxicity include age (both neonatal and geriatric patients), fever, sepsis and dehydration.
DOSAGE AND ADMINISTRATION
Cattle, Sheep and Goats:
7 mg/kg IV, IM q8h
22 mg/kg IV, IM q24h [once daily dosing]
Horses:
22 - 25 mg/kg IV q24h for neonates
5 mg/kg IV q24h for older foals and adults
Adults : 6.6 - 10 mg/kg IM, IV q24h [once daily dosing]
Mastitis / Endometritis : 8 ml of MICIX Inj mixed with 200 mL 0.9%
Sodium Chloride Injection, daily for 3 - 5 consecutive days
[intrauterine/intramammary use]
POULTRY :
10 mg/kg b.wt. S/C or I/M injection
WITHDRAWAL PERIOD
Eggs : 7 days
Meat : 28 days
PACK SIZE
10 ml, 50 ml & 100 ml Vial
MICIX





































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NEROCIN - Injection of Methylcobalamin, Vitamin B6 & Nicotinamide

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
NEROCIN






















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NOLON - Triamcinolone Injection BP 6 MG/ML

COMPOSITION
Each ml contains:
Triamcinolone Acetonide BP    6 mg
Benzyl Alcohol BP    0.9% w/v
Water for injection BP    Q.S.
INDICATIONS
  • Bovine Ketosis
  • Arthritis
  • Tenosynovitis and related disorders
  • Dermatological Disorders including pruritus
  • Allergic reactions and dermatoses
  • Haematoma
  • Inflammatory conditions
  • Pregnancy toxaemia in ewes/sheep
CONTRA-INDICATIONS
Use of triamcinolone is contraindicated in systemic fungal infections, animals with arrested tuberculosis, peptic ulcer, acute psychoses, corneal ulcer, & Cushingoid syndrome. The presence of diabetes, osteoporosis, chronic psychotic reactions, predisposition to thrombophlebitis, hypertension, CHF, renal insufficiency, & active tuberculosis necessitates carefully controlled use. In dogs, polydipsia (PD), polyphagia (PP), and polyuria (PU) may all be seen with short-term “burst” therapy as well as with alternate-day maintenance therapy on days when giving the drug.
DOSAGE AND ADMINISTRATION
Bovine Ketosis :
2.5 mg to 10 mg given in a single intramuscular injection.
        
   
AnimalIntra-Articular/IntrasynovialIntramuscular/Sub-cutaneously in Arthritic or Allergic conditions
Horses/Cattle/Camel 6 to 18 mg12 to 20 mg
Dogs & Cats1 to 3 mg0.1 to 0.2 mg per kg
WITHDRAWAL PERIOD
Milk : Nil
Meat : Nil
PACK SIZE
5 ml, 10 ml Vial
NOLON






















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PAXON - Parvaquone injection 150 mg/ml

COMPOSITION
Each ml contains :
Parvaquone         150 mg
Sorbitan Mono Oleate B.P  100 mg
(as preservative)
Oil base          q.s.
INDICATIONS
East Coast Fever (ECF, Theileria parva infection) of Cattle. Parvaquone kills the schizont and piroplasm state of parasites. The product may be used in animal showing clinical signs of Theileriosis and it can be also used as prophylaxis in infected animals which are not showing the signs.
CONTRA-INDICATIONS
Parvaquone shows no any side effects with any other commonly used veterinary products.
DOSAGE AND ADMINISTRATION
Intramuscular route into the neck muscles.
Calves : 1 ml per 50 kg
Adults:
Body weight   Dose
100 kg      7ml
150 kg      10ml
200 kg      14ml
250 kg      17ml
300 kg      20ml
WITHDRAWAL PERIOD
Milk : 14 days
Meat : 28 days
PACK SIZE
50 ml, 100 ml Vial
PAXON






















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PAXON PLUS - Parvaquone and Furosemide injection

COMPOSITION
Each ml contains :
Parvaquone         150 mg
Furosemide B.P       55 mg
Sorbitan Mono Oleate B.P  100 mg
( as preservative )
Oil base           q.s.
INDICATIONS
PAXON PLUS is a potent Injection treatment for theileriosis (East Coast Fever) particularly for advanced cases with pulmonary oedema.
Parvaquone is theilericidal, acting on schizonts and piroplasms:
Frusemide is a diuretic, which resolves pulmonary oedema.
DOSAGE AND ADMINISTRATION

Inject by the Intramuscular route into the neck muscles at the rate of 1 ml/50 kg (10.0 mg Parvaquone, 3.6 mg Furosemide per kg). Repeat after 48 hours. In case of exceptionally server infections with pulmonary oedema, further treatment at half the dosage rate may be required at 24 hour intervals. Calves : 1 ml/50 kg body weight Young-stock and adults:

Body weight   Dose
100kg      7ml
150kg      10ml
200kg      14ml
250kg      17ml
300kg      20ml

Alternatively. When pulmonary symptoms have been resolved by PAXON PLUS, treatment to achieve parasitic cure may be completed with PAXON which contains only Parvaquone, at a dose rate of 1 ml/50 kg every 48 hours. Do not use by the Intravenous or Subcutaneous route. Normal asceptic precautions should be observed

WITHDRAWAL PERIOD
Milk : 14 days
Meat : 28 days
PACK SIZE
50 ml, 100 ml Vial
PAXON PLUS































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PROFEN - Ketoprofen 100 mg/ml injection

COMPOSITION
Each ml contains :
Ketoprofen       100 mg
Benzyl Alcohol B.P    1% w/v
Water For Injection B.P  q.s.
INDICATIONS
Inflammatory and painful conditions of the bones and joints and muscle-skeletal systems in horses. Colic in horses. Respiratory infection and acute clinical mastitis in cattle. Respiratory infection in pig and Mastitis-Metritis-Agalactia syndrome in sows.
CONTRA-INDICATIONS
Hypersensitivity to ketoprofen.
Concurrent administration or administration of other non-steroidal anti-inflammatory drugs within 24 hours.
Administration in animals suffering from cardiac, hepatic or renal disease.
Administration to pregnant mares, because the effects of ketoprofen on fertility, pregnancy or foetal health of horses have not been determined.
DOSAGE AND ADMINISTRATION
Horses : 1.0 ml per 45 kg body weight by intravenous injection once daily for up to 3 to 5 days
Cattle : 1.0 ml per 33 kg body weight by intravenous or deep intramuscular injection once daily for up to 3 days.
Pigs : 1.0 ml per 33 kg body weight once by deep intramuscular injection.
WITHDRAWAL PERIOD
Cattle : Milk : Nil
Meat : 4 days
Horse : Meat : 28 day
PACK SIZE
100 ml Vial
PROFEN


























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SELEXIDANT - Vitamin E and Selenium Injection

COMPOSITION
Each ml contains :
Vitamin E, α-tocopherol acetate  50 mg
Sodium selenite pentahydrate
equi. To selenium         0.30 mg
Benzyl alcohol B.P        2% v/v
Water for Injection B.P      q.s.
INDICATIONS
Vitamin E deficiencies (like encephalomalacia, muscular dystrophy, exudative diathesis, infertility problems) in Calves, Goats, Sheep and Swine.
Prevention of iron intoxication after administration of iron to Piglets.
DOSAGE AND ADMINISTRATION
For Intramuscular or Subcutaneous administration.
Calves, Goats and Sheep :
2 ml per 10 kg body weight, repeat after 2-3 weeks.

Swine :
1 ml per 10 kg body weight, repeat after 2-3 weeks.
WITHDRAWAL PERIOD
For meat : 0 days
For milk : 0 days
PACK SIZE
100 ml Vial
SELEXIDANT






















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SIPHOS-12 - Sodium Acid Phosphate With Vitamin B12 Injection

COMPOSITION
Each ml contains:
Sodium acid phosphate B.P    40% w/v
Equi. to Elemental Phosphorous  79.4 mg
Cynocobalamin B.P        50 mcg
Methyl Hydroxybenzoate B.P    0.18% w/v
Propyl Hydroxybenzoate B.P    0.02% w/v
Water for injection B.P      q.s.
INDICATIONS
It is indicated for infertility cases such as under developed Genitalia, Delayed, maturity, Anoestrus and maintainance of pregnancy. It is very effective to treat Metabolic disorders such as : Post parturient Haemoglobinuria, Hypophosphataeimia, Ketosis & Milk Fever. It is useful in General debility conditions and in the treatment of Bloat, Tetany, pica & Rickets in lambs.
Folic Acid acts in synergy in the formulation of DNA, and deficiencies can have serious consequences, both in performance horses with a high tissue turnoverA rate, and in pregnancy and growth of young foals.
Clinically the first sign of deficiency is anaemia. Vitamin B12 is essential to the formation of FOLIC ACID. It is useful to stimulate appetite in horses, and is essential maintainance of adequate blood counts.
DOSAGE AND ADMINISTRATION
Large animals : 5-10 ml daily for alternate days.
Small animals : 2-5 ml daily dose can be adjusted according to the phosphorous need of the animal. It is advisable to administer half the dose by s/c route in several places.
WITHDRAWAL PERIOD
Nil
PACK SIZE
100 ml Vial
SIPHOS-12






















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THIACIN 500 Thiamine Injection

COMPOSITION
Each ml Contains:
Thiamine hydrochloride BP   500 mg
(Vitamin B1)
Water for Injection BP      q.s.
ACTION
THIACIN 500 Injection provides the essential vitamin Thiamine. THIACIN 500 plays an important role in the metabolism of carbohydrates, and energy production for all cells. Thiamine is most important in the breakdown of pyruvic acid, a waste product in hard working muscles, along with lactic acid.
In any situation where carbohydrates are the major energy source, or when glucose is added to the diet, thiamine requirement is increased significantly.
Thiamine is essential as part of the coenzyme which is involved in the breakdown of glucose for energy. Thiamine, in conjunction with Vitamin B6 (Pyridoxine) is essential in the metabolism of proteins and amino acids, Thiamine has effects on all tissues. The most sensitive are nerves, stomach and heart. Thiamine can not store in the body, and it is rapidly absorbed from the intestine or blood, as well as from injection sites. Like all B Complex vitamins, Thiamine is water soluble, so it is rapidly absorbed and excreted from the body, and requires regular supplementation, especially in hard working animals when dietary input will probably not be sufficient. Thiamine is found in both meat and cereal products. Small amounts are manufactured in the gut, as long as Horses are not under stress. Thiamine in food is destroyed by cooking. High dose of thiamine are reported to help calm nervous or over excitable Horses. Clinical signs of thiamine deficiency include fatigue, muscle weakness, loss of appetite and increased heart rate. (This may be an important factor in endurance Horses fed high grain diets). Many of these signs can be traced back to increased tissue levels of lactic and pyruvic acids. Nerve cells are particularly dependant on carbohydrate metabolism, and normal nerve function is greatly affected by increased levels of these acids during hard work.
DOSAGE AND ADMINISTRATION
Dogs : 1 to 10 mg
Cats : 0.5 to 5 mg
Horses, Cattle and Swine : 100 mg Per 100 kg of body weight.
Administer intramuscularly, once daily Or as recommended by the veterinarian
WITHDRAWAL PERIOD
Meat: Nil
PACK SIZE
100 ml Vial
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TROXIN - Ceftriaxone Sodium Powder for Injection

COMPOSITION
Each vial contains :
Ceftriaxone Sodium B.P
equi. to Ceftriaxone anhydrous   3 g
INDICATIONS
Preoperative prophylaxis, post operative treatment, haemorrhagic septicemia, broncho pneumonia, nephritis, cystitis, endometritis, metritis, pyometra, mastitis, actionbacillosis, bacterial meningitis and septicaemia.
CONTRA-INDICATIONS
Ceftriaxone is contraindicated in animal with known allergy to cephalosporin class of antibiotics. Careful inquiry should be made to determine whether the animal has had a previous history of hypersensitivity reaction to cephalosporins, penicillins or other drugs.
Biliary elimination occurs and hence, Ceftriaxone should be given cautiously to those species of animal with extended large intestines e.g. Horse.
DOSAGE AND ADMINISTRATION
I.M / I.V USE
TROXIN 3g Injection should be diluted with 10 ml WFL and injected at 12-24 hours interval. It can be administered either intramusculary or intravenously.
Large animals : 7.5 - 25ml / 50kg body weight.
Calf and Goat : 1.5 - 5ml / 10kg body weight.
Dogs : 1.5 - 5ml / 10kg body weight.
Cat : 0.25 - 0.5 ml/kg body weight.
WITHDRAWAL PERIOD
Milk : 7 days
Meat : 28 days
PACK SIZE
3 gm in 20 ml Vial
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VITCIN - Multivitamin Injection

COMPOSITION
Each ml contains :
Vitamin A [palmitate] B.P       10000 I.U.
Thiamine Hydrochloride B.P      50mg
Riboflavin Phosphate Sodium B.P    10 mg
Nicotinamide B.P           100 mg
D-Panthenol USP           25 mg
Pyridoxine Hydrochloride B.P      15 mg
Ascorbic Acid B.P           500 mg
Vitamin E Acetate B.P   
[Tocopheryl Acetate B.P]        5 mg
Benzyl Alcohol B.P [as preservative]   1.5% w/v
Water for Injection. B.P         Q.S.
INDICATIONS
VITCIN is well balanced combination of essential vitamins and amino acids for cattle, goats, sheep and swine. VITCIN is used for:
-Prevention or treatment of vitamin or amino acid 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.
CONTRA-INDICATIONS
Do not administer to calves, horses, foals, kids and lambs.
DOSAGE& Admin.
For subcutaneous or intramuscular administration.
Cattle : 10-15 ml.
Goats and Sheep : 5-10 ml.
Swine : 2-10 ml.
Pack Size
100 ml Vial



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VIT-K - Menadione Sodium bisulfite Vitamin k Injection

COMPOSITION
Each ml contains :
Menadione sodium bisulfite  10 mg
Water for Injection B.P    q.s.
INDICATIONS
Hypoprothrombinemia; hemorrhages due to Vitamin K deficiencies.
DOSAGE AND ADMINISTRATION
By a single Subcutaneous, Intramuscular or Intravenous Injection.
Horses, Cattle : 10 - 12 ml
Calves : 2 - 5 ml
Dogs and Cats : 0.1 - 1 ml
Sheep and Goats : 0.05 - 0.25 ml/kg body weight daily
WITHDRAWAL PERIOD
Nil
PACK SIZE
100 ml Vial
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Water Soluble Powder for Equine (Horse)

DX-CURE - Dexamethasone & Hydrochlorothiazide Powder

COMPOSITION
Each gram contains:
Dexamethasone Sodium Phosphate B.P.   0.25 mg
Hydrochlorothiazide B.P.           75 mg
Excipient                 1 g
INDICATIONS
  • Generalised congestion and oedema
  • Oedema of sheath
  • Anasarca
  • Oedema in allergic conditions

CONTRA-INDICATIONS
Do not use in:
  • Pregnant animals.
  • Animals with viral infections, during the viraemic phase.
  • Animals with diabetes mellitus, congestive heart failure, chronic nephritis, osteoporosis or glaucoma.
  • Animals with hepatic encephalopathy.
  • Cases of severe hypokalaemia.
  • Animals with known hypersensitivity to the active ingredients.

DOSAGE AND ADMINISTRATION
For oral administration via drinking water.
Adult Cattle and Horses: 2 sachet on the 1st day. 1 sachet on the 2nd and 3rd days (2 g/ 25-50 kg body weight).
WITHDRAWAL PERIOD
Meat and offal : 6 days.
Milk : 3 days.
PACK SIZE
Sachet of 20 g.
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PIZINE WS - Piperazine Citrate Powder

COMPOSITION
Each gram contains:
Piperazine citrate B.P  1000 mg
INDICATIONS
Nematode infections in Horses, Swine, Cattle and Poultry.
Swine : Oesophagostomum and Ascaris.
Cattle : Ascaris, Nematodirus, Ostertagia, Cooperia and Oesophagostomum.
Horses : Strongylus, Oxyuris, Trichonema and Ascaris.
Poultry : Ascaris and Capillaria.
CONTRA-INDICATIONS
  • Hypersensitivity to piperazine.
  • Administration to animals with a seriously impaired hepatic and/or renal function.
DOSAGE AND ADMINISTRATION
For oral administration:
Horses, Swine and Cattle : 1 - 2 g per 10 kg body weight through drinking water.
Poultry : 1 kg per 1000 litres of drinking water for 2 days.
WITHDRAWAL PERIOD
For meat : 2 days.
For eggs : 2 days.
PACK SIZE
Sachet of 100 g and jar of 1000 g
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