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Intracin Pharmaceuticals Pvt. Ltd.WHO GMP Accredited Company
Intracin Pharmaceuticals Pvt. Ltd.WHO GMP Accredited Company


Veterinary Injectable 1

We are the leading manufacturer of veterinary formulations for different species like Cattle, Goat, Pets, Calves, Horse,Buffalo, Camel, Poultry, Pig, Sheep, Swine, Calf etc.

Ambroxol Hydrochloride Injection 6 mg/ml (Vet)

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Ambroxol Hydrochloride Injection 6 mg/ml (Vet)
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COMPOSITION:

Each ml contains:

Ambroxol Hydrochloride BP          6 mg

Water for Injection BP                   Q.S.

 

INDICATION :

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, catarrrhinitis, strangles, post-viral cough

Uterine infections : pyometron, mucometron

Ocular Infections : purulent conjuctivities, hypopion

 

ACTION :

ABXOL is a mucolytic expectirant. 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

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Atropine injection

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Atropine injection
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Composition:

Each ml contains:

Atropine sulfate                                15 mg

Sodium Chloride                                 9 mg

Benzyl Alcohol(preservative)                  1%

Water for Injection                                q.s.

The pH is adjusted with sulfuric acid and/or sodium hydroxide if necessary.

 

DOSAGE AND ADMINISTRATION:

Initial Dose:

Cattle : 30 mg per 100 lbs. of body weight

Horses : 6.5 mg per 100 lbs. of body weight

Sheep : 50 mg per 100 lbs. of body weight

 

The recommended average initial dose should be split,injecting ¼ to 1/3 slowly intravenously,and the remainder intramuscularly or subcutaneously.After symptoms appear to be under control,repeated maintainance doses should be administered based upon the individual response of the animal.

 

PACK SIZE:

100 ml vial

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Buparvaquone Injection 50 mg/ml

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Buparvaquone Injection 50 mg/ml
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COMPOSITION :

Each ml contains :

Buparvaquone                               50 mg

Sorbitan mono oleate B.P.            100 mg

Oil Base                                            q.s.

 

INDICATION :

It is indicated for theileriosis (East Coast Fever, Corridor Disease, Zimbabwean Theileriosis, Thopical Theileriosis) caused by intracellular protozoan parasites Theileria parva Theileria parvabovis, Theileria parva lawrencai, T.annulata, T.mutans and T.orientalis sergenti in cattle. It is active against both the schizont and piroplasm stage of Theileria spp., and may be used during the incubation period of the disease or  when clinical signs are apparent.

 

CONTRAINDICATION :

Due to the inhibiting effects of theileriosis on the immune system, Vaccination should be delayed until the animal has recovered from theileriosis.

 

DOSAGE AND ADMINISTRATION :

A single dose of 1 ml BUPACIN Injection per 20 kg bodyweight.(2.5 mg buparvaquone per kg bodyweight). In severe cases the treatment may be reaoeted within 48-72 hours. Not more than 10 ml should be injected into a single site. Successive Injection should be administered at different sites.

 

ADMINISTRATION :

Intramuscular Injection into the neck muscles.

 

WITHDRAWAL PERIOD :

Milk : 2 days

Meat : 42 days

 

PACK SIZE :

20 ml 50 ml Vial

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Buparvaquone With Furosemide Injection

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Buparvaquone With Furosemide Injection
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Composition:

Each ml contains :

Buparvaquone                                                    50 mg

Furosemide  BP                                                  55 mg

Sorbitan mono oleate  BP   100 mg ( as preservative )

Oil base                                                                 Q.S.

 

Indications:

It is indicated for theileriosis (East Coast Fever, Corridor Disease, Zimbabwean Theileriosis, Thopical Theileriosis) caused by intracellular protozoan parasites Theileria parva Theileria parvabovis, Theileria parva lawrencai, T.annulata, T.mutans and T.orientalis sergenti in cattle. It is active against both the schizont and piroplasm stage of Theileria spp., and may be used during the incubation period of the disease or  when

clinical signs are apparent.

 

Contra-indications:

Due to the inhibiting effects of theileriosis on the immune system,

Vaccination should be delayed until the animal has recovered

from theileriosis.

 

 

Dosage:

A single dose of 1 ml BUPACIN Injection per 20 kg bodyweight.(2.5 mg

buparvaquone per kg bodyweight). In severe cases the treatment may

be reaoeted within 48-72 hours. Not more than 10 ml should be

injected into a single site. Successive Injection should be administered

at different sites.

 

Withdrawal times:

Milk : 2 days

Meat : 42 days

 

Packaging:

 

50ml, 100ml vial

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Butaphosphan and Cyanocobalamin Injection

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Butaphosphan and Cyanocobalamin Injection
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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.

 

INDICATION :

Metabolic disorders of different etiologies.

 

DOSAGE AND ADMINISTRATION :

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.

 

WITHDRAWAL PERIOD :

Meat : None

Milk : None

Egg : None

 

PACK SIZE :

100 ml Vial

 

 

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Calcium Levulinate, Vitamin D3 7 Vitamin B12 Injection

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Calcium Levulinate, Vitamin D3 7 Vitamin B12 Injection
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COMPOSITION :

Each ml contains :

Calcium Levulinate USP…………..76.4mg

(eq. to 10 mg of lonic Calcium)

*Cholecalciferol BP……………….5000 IU

*Cyanocobalamin  BP…………….50 mcg

 Benzyl alcohol BP………………….1.5% v/v

Water for injection BP…………………..q.s.

*Required overages are added.

 

INDICATION :

Prevention and treatment of hypocalcaemia , debility , weakness , to improve health productivity and milk yield.

 

DOSAGE AND ADMINISTRATION :

For intramuscular use:

Cattle and buffalo (Prepartum)                       10-15ml thrice/week

Cattle and buffalo (postpartum)                      15-20ml thrice/week

Cattle and buffalo (for other  condition)                10ml thrice/week

Small animals                                                      1-5ml thrice/week

Or as directed by Veterinarian.

 

PACK SIZE :

100 ml Vial

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Chlorphenamine Injection B.P. 10 mg/ml(Vet)

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Chlorphenamine Injection B.P. 10 mg/ml(Vet)
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COMPOSITION :

Each ml contains :

Chlorphenamine maleate B.P. 10 mg

Phenyl mercuric nitrate B.P. 0.002 % w/v

(As Preservative)

Water for injection B.P. q.s.

 

INDICATION :

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 ruminant.

5. Puerperal toxaemia and secondary placental retention, acute septic metritis and gangrenous mastitis.

6. Reactions and other drug allergies and anaphylactic shock.

 

CONTRAINDICATION :

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 :

100 ml Vial

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Closantel 10% w/v Injection

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Closantel 10% w/v Injection
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Composition:

Each ml contains :

Closantel 100mg

Benzyl alcohol B.P 2% 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

larvea), 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:

1ml/50kg of bodyweight by Subcutaneous Injection only

 

Withdrawal times:

Meat : 49 days

Packaging:

50ml,100ml vial

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Closantel 5% w/v Injection

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Closantel 5% w/v Injection
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Composition:

Each ml contains :

Closantel                          50mg

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 larvea),

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:

2ml/50kg of bodyweight by Subcutaneous Injection only

 

Withdrawal times:

Meat  :  49  days

 

Packaging:

100ml vial

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Cyanocobalamin Injection USP

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Cyanocobalamin Injection USP
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COMPOSITION :

Each ml contains :

Cyanocobalamin                BP           500 mcg

Benzyl alcohol                    BP           1.5% v/v

Water For Injection             BP                 Q.S.

 

ACTION :

Vitamin B12 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 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 anaemia. 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. Vitamin B12 is involved in the formation of the amino acids methionine and glycine, as well as the vitamin choline. Vitamin B12 supplementation is highly recommended during pregnancy, as deficiencies in young growing animals are often associated with retardation. Cooking and storage of feeds destroy Vitamin B12 levels. When antibiotics, particularly sulphur drugs, are used for extended periods, the normal synthesis of Vitamin B12 in the gut will be reduced, and the requirement for Vitamin B12 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 :

Nil

 

PACK SIZE :

100 ml Vial

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Dexamethasone Sodium Phosphate Injection B.P.(Vet)

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Dexamethasone Sodium Phosphate Injection B.P.(Vet)
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COMPOSITION :

Each Vial contains :

Dexamethasone sodium phosphate B.P.

eq. dexamethasone

Phosphate ... ........................................ 4 mg.

Methyl Hydroxybenzoate B.P. ... 0.15% w / v

Propyl Hydroxybenzoate B.P. .......................... 0.02% w / v

(As Preservatives)

Water for injection B.P..............................q.s.

 

INDICATION :

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.

 

CONTRAINDICATION :

Except in Emergency Situations, Do not Use in animals suffering from diabetes mellitus, Renal Insufficiency.Cardiac in sufficiency, hyper aadrenocorticism 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 demodicosts.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

Horse, Cattle, Pig : 0.06 mg/kg body weight

Dog, Cat : 0.1 mg/kg body weight

DEXACIN can be administrated by Intravenous or intramuscular injection in horses and by intramuscular injection in Cattle, Pig, Dogs and Cats.

 

WITHDRAWAL PERIOD :

Milk : 4 days Meat : 28 days

PACK SIZE :

5 ml Vial

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Dichloro Acetic Acid Injection

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Dichloro Acetic Acid Injection
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COMPOSITION :

Each ml contains :

Dichloro-acetic acid                            120 mcg

Sodium gluconate USP                        250 mg

Water For Injection  BP                             Q.S.

 

ACTION :

I-CLOR contains dichloroacetic acid, which is an activator of the enzyme pyruvate dehyfrogenase. This enzyme plays a central role in the process of lactic acid production during hard work. Supplementation with dichloroacetic acid (DCA) 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 DCA 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 execise, have been used to assist in the prevention of Typing Up in horses. Similarly, DCA (LACTANASE) 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

 

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Diminazene Aceturate 7% Injection

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Diminazene Aceturate 7% Injection
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COMPOSITION :

Each ml contains :

Diminazene Aceturate                           70 mg

Phenazone name (ANTIPYRINE)        375 mg

Water for Injection                                      q.s

 

 

INDICATION :

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

 

CONTRAINDICATION :

Hypersensitivity to diminazene or phenazone.

 

DOSAGE AND ADMINISTRATION :

Inject subcutaneously or intramuscularly, May be injected intravenously at the discretion of the veterinarian.

Cattle, Horses, Swine and Sheep – 1 to 2 ml.

Dogs and Cats – 0.25 to 0.5 ml.

Suggested dosage may be repeated at 1 to 2 week intervals, as indicated by condition and response.

 

WITHDRAWAL PERIOD :

Meat : 21 days

Milk : 3 days

 

PACK SIZE :

100 ml Vial

 

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Enrofloxacin Injection 10% w/v(Vet)

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Enrofloxacin Injection 10% w/v(Vet)
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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.

 

INDICATION :

Sheeping fever pneumonia(H.S.), Pneumonia, Pleuropneumonia, Pseudorinderpestand 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 is effective against the following microoganisms: Mycoplasma spp., E.coil, Salmonella spp., Haemophilus spp., Pasteurella spp., Klebsiella spp., Proteus spp., Vibrio parahaemolyticus and Staphylococcus aureus.

 

CONTRAINDICATION :

Do not exceed the recommended dose. In accidental overdosage there is no antidote and treatment should be symptomatic.

 

DOSAGE AND ADMINISTRATION :

Cattle, Buffaloes, Sheep, Goats and Camels :

The dose rate is 2.5 mg Enrofloxacin per kg body weight(2.5 ml IROFLOX inj. Solution per 100 kg body weight) For complicated respiratory disease or to check secondary complication in viral infection this rate may be doubled to 5 mg per kg body weight (5ml IROFLOX inj. Solution per 100 kg bw). 

 

WITHDRAWAL PERIOD :

Meat :

Subcutaneous use - Animals must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 14 days from the last treatment.

intravenous use - Animal must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 4 days from the last treatment.

 

 

 

 

 

 

 

 

 

Milk :

Subcutaneous use - Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from Cattle after 84 hours (i.e. milking from the last treatment).

Intravenous use - Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from Cattle after 72 hours (i.e. 6 milking from the last treatment)

 

PACK SIZE :

15 ml, 30 ml, 50 ml and 100 ml Vial

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Enrofloxacin Injection 20% w/v(Vet)

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Enrofloxacin Injection 20% w/v(Vet)
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COMPOSITION :

Each ml contains :

Enrofloxacin             USP           200 mg

Benzyl Alcohol         B.P.          3.0 % v/v

(as preservative)

Water for Injection    B.P.                 q.s.

INDICATION :

Sheeping fever pneumonia(H.S.), Pneumonia, Pleuropneumonia, Pseudorinderpestand 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 is effective against the following microoganisms: Mycoplasma spp., E.coil, Salmonella spp., Haemophilus spp., Pasteurella spp., Klebsiella spp., Proteus spp., Vibrio parahaemolyticus and Staphylococcus aureus.

CONTRAINDICATION :

Do not exceed the recommended dose. In accidental overdosage there is no antidote and treatment should be symptomatic.

DOSAGE AND ADMINISTRATION :

Cattle, Buffaloes, Sheep, Goats and Camels :

The dose rate is 2.5 mg Enrofloxacin per kg body weight.

WITHDRAWAL PERIOD :

Meat :

Subcutaneous use - Animals must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 14 days from the last treatment.

intravenous use - Animal must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 4 days from the last treatment.

Milk :

Subcutaneous use - Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from Cattle after 84 hours (i.e. milking from the last treatment).

Intravenous use - Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from Cattle after 72 hours (i.e. 6 milking from the last treatment)

PACK SIZE :

15 ml, 30 ml, 50 ml and 100 ml Vial

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Flunixin Meglumine Injection USP(Vet) 5% w/v

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Flunixin Meglumine Injection USP(Vet) 5% w/v
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COMPOSITION :

Each ml contains :

Flunixine meglumine USP

equi. to flunixin                                            50 mg

Phenol B.P.                                              0.5%w/v

(As Preservative)

Water for Injection B.P.                                   q.s.                     

 

INDICATION :

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 & 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 :

100 ml Vial

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Folic Acid Injection B.P.

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Folic Acid Injection B.P.
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COMPOSITION :

Each ml contains :

Folic acid BP 15 mg

Water For Injections BP 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 maintenance 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 anaemia. 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 is 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

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Fortified Procaine Penicillin Injection 20, 00000 Units

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Fortified Procaine Penicillin Injection 20, 00000 Units
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COMPOSITION :

Each vial contains :

Procaine Penicillin G B.P.               15, 00, 000 units

Penicillin G Sodium B.P.                   5, 00, 000 units

 

INDICATION :

Cattle, Buffalo, Horses, Sheep, Goat, Dog, Cat :

Actiomycosis, anthrax, black quarter, calf diphtheria, foot rot, leptospimsis, malignant oedema, pneumonia, navel ill, abscess, mastitis, metritis, strangles, bacterial influenza, bronchitis, castration, pyogenic infections, urinary tract infections.

 

CONTRAINDICATION :

Fortified Procaine Penicillin Injection (20,00,000 units) is contraindicated in animals hypersensitive to active ingredients.

 

DOSAGE AND ADMINISTRATION :

By deep intra-muscular injection only. Fortified Procaine Penicillin Injection (2000000 units) should be diluted with 10ml water for Injection and Injected at 24 hours interval. The drug should be used for 1-2 more days after relief of symptoms.

For Cow, Buffalo, Horse, Sheep &Goat : Daily dose of ;

0.2-0.5 ml per 10 kg bodyweight

1-2.5 ml per 50 kg bodyweight

2-5 ml per 100 kg bodyweight

4-10 ml per 200 kg bodyweight

 

WITHDRAWAL PERIOD :

Species                            Withdrawl Time(days)   Milk Discard Time (days)

Cattle, Buffalo & Horse      10(at label dosage)                           3

                                          30(at 20, 000 IU/kg, bid)

Sheep & Goat                    9                      

 

PACK SIZE :

1 x 20, 00, 000 units in 10 ml Vial pack

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Fortified Procaine Penicillin Injection 40, 00000 Units

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Fortified Procaine Penicillin Injection 40, 00000 Units
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COMPOSITION :

Each vial contains :

Procaine Penicillin G B.P.               30, 00, 000 units

Penicillin G Sodium B.P.                 10, 00, 000 units

 

INDICATION :

Cattle, Buffalo, Horses, Sheep, Goat, Dog, Cat :

Actiomycosis, anthrax, black quarter, calf diphtheria, foot rot, leptospimsis, malignant oedema, pneumonia, navel ill, abscess, mastitis, metritis, strangles, bacterial influenza, bronchitis, castration, pyogenic infections, urinary tract infections.

 

CONTRAINDICATION :

Fortified Procaine Penicillin Injection (40,00,000 units) is contraindicated in animals hypersensitive to active ingredients.

 

DOSAGE AND ADMINISTRATION :

By deep intra-muscular injection only. Fortified Procaine Penicillin Injection (4000000 units) should be diluted with 10ml water for Injection and Injected at 24 hours interval. The drug should be used for 1-2 more days after relief of symptoms.

For Cow, Buffalo, Horse, Sheep &Goat : Daily dose of ;

0.2-0.5 ml per 10 kg bodyweight

1-2.5 ml per 50 kg bodyweight

2-5 ml per 100 kg bodyweight

4-10 ml per 200 kg bodyweight

 

WITHDRAWAL PERIOD :

Species                            Withdrawl Time(days)   Milk Discard Time (days)

Cattle, Buffalo & Horse      10(at label dosage)                           3

                                          30(at 20, 000 IU/kg, bid)

Sheep & Goat                    9                      

 

PACK SIZE :

1 x 40, 00, 000 units in 20 ml Vial pack

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Furosemide Injection BP 5% w/v

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Furosemide Injection BP 5% w/v
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COMPOSITION :

Each ml contains :

Furosemide Sodium B.P. equi.to Furosemide               50 mg

Benzyl Alcohol B.P.(as preservative)                           1% v/v

Water for Injection B.P.                                                     q.s.

 

INDICATION :

It is used for treatment of congestive cardio myopathy, 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 hepls to prevent or to reduce epistaxis.

 

CONTRAINDICATION :

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 human consumption.

Cattle: Meat & Milk : 48 hours.

 

PACK SIZE :

100 ml vial

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Gentamicin Injection B.P. 40mg/ml (Vet)

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Gentamicin Injection B.P. 40mg/ml (Vet)
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COMPOSITION :

Each ml contains :

Gentamicin Sulphate B.P.

equivalent to Gentamicin.....................................40 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.       

 

INDICATION :

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.

 

CONTRAINDICATION :

Gastrointestinal respiratory infections, arthritis, poly-arthritis, meningitis, mastitis & metritis caused by Gentamicin sensitive bacteria, like E-coli, Pasteurella, Klebseilla and Salmonella spp., in Calves, Cattle, Horse, Goats and Sheep

 

DOSAGE AND ADMINISTRATION :

Large Animal : 2-4 mg/kg bodyweight I.M., I.V. or SC.

Small Animals : 1-2 mg/kg bodyweight I.M. or I.V.

For intramuscular or slow intravenous injection.

Poultry : 0.05ml per kg bodyweight

Horses & Cattle: 4.00ml per 100 kg bodyweight

Foaks & Calves: 2.00ml per 500 kg bodyweight

Dogs & Cats: 0.25ml per 5kg bodyweight

These does preferably to be given twice on the 1st day and afterwards once daily.

 

WITHDRAWAL PERIOD :

For meat : 7 days

For milk : 3 days

 

PACK SIZE :

100 ml Vial

 

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Gentamicin Injection B.P. 40mg/ml (Vet)

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Gentamicin Injection B.P. 40mg/ml (Vet)
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COMPOSITION :

Each ml contains :

Gentamicin Sulphate B.P.

equivalent to Gentamicin.....................................40 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.       

 

INDICATION :

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.

 

CONTRAINDICATION :

Gastrointestinal respiratory infections, arthritis, poly-arthritis, meningitis, mastitis & metritis caused by Gentamicin sensitive bacteria, like E-coli, Pasteurella, Klebseilla and Salmonella spp., in Calves, Cattle, Horse, Goats and Sheep

 

DOSAGE AND ADMINISTRATION :

Large Animal : 2-4 mg/kg bodyweight I.M., I.V. or SC.

Small Animals : 1-2 mg/kg bodyweight I.M. or I.V.

For intramuscular or slow intravenous injection.

Poultry : 0.05ml per kg bodyweight

Horses & Cattle: 4.00ml per 100 kg bodyweight

Foaks & Calves: 2.00ml per 500 kg bodyweight

Dogs & Cats: 0.25ml per 5kg bodyweight

These does preferably to be given twice on the 1st day and afterwards once daily.

 

WITHDRAWAL PERIOD :

For meat : 7 days

For milk : 3 days

 

PACK SIZE :

100 ml Vial

 

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Imidocarb Dipropionate Aqueous Injection Solution

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Imidocarb Dipropionate Aqueous Injection Solution
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COMPOSITION :

Each ml contains :

Imidocarb Dipropionate                         120 mg

Benzyl Alcohol B.P.                              2.0%w/v

Water For Injection B.P.                              Q.S.

 

INDICATION :

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 bodyweight.

Sheep : 0.5 ml per 50 kg bodyweight.

Horses : 2 ml per 10 kg bodyweight. (Intramuscular injection is preferred). In most cases, a single dose will effect a complete cure, but the treatment of B. equi infections in horses may require 2 doses at an interval of 24 hours.

Dogs : 0.25 ml per 10 kg bodyweight. In treating mixed infection due to Ehrlichin 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 if the test is positive.

 

WITHDRAWAL PERIOD :

Milk : 7 Days

Meat : 28 Days

 

PACK SIZE :

100 ml Vial

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Ivermectin And Clorsulon Injection U.S.P.(Vet) 100 ml

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Ivermectin And Clorsulon Injection U.S.P.(Vet) 100 ml
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COMPOSITION :

Each ml contains :

Ivermectin B.P.                                             10 mg

Clorsulon U.S.P.                                         100 mg

Benzyl Alcohol (as preservative)B.P.        1.5% v/v

Propylene Glycol B.P.                                      q.s. 

 

INDICATION :

For treatment and control of gastrointestinal immature and adult roundworms.

Lung Worms : Both adult and Fourth - Stage larvae of Dictyocaulus viviparous.

Liver Flukes : Immature and adult Fasciola hepatica & Fasciolagigantica.

Eye Worm : Thelazia app. Ectoparasites (Dermatobiahominis, Psoroptesbovis) Including Sucking Lice, Ticks & Mites.

 

CONTRAINDICATION :

Administration to lactating animals and pregnant heifers within 60 days of Calving. This product is not for intravenous or intramuscular use.

 

DOSAGE AND ADMINISTRATION :

For subcutaneous administration.

General : 1.0 ml per 50 kg bodyweight

Cattle : 1 ml per 50 kg bodyweight

Sheep & Goat : 0.5 ml per 25 kg bodyweight

 

WITHDRAWAL PERIOD :

For meat : 35 days

 

PACK SIZE :

100 ml Vial

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Ivermectin And Clorsulon Injection U.S.P.(Vet) 100 ml

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Ivermectin And Clorsulon Injection U.S.P.(Vet) 100 ml
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COMPOSITION :

Each ml contains :

Ivermectin B.P.                                             10 mg

Clorsulon U.S.P.                                         100 mg

Benzyl Alcohol (as preservative)B.P.        1.5% v/v

Propylene Glycol B.P.                                      q.s. 

 

INDICATION :

For treatment and control of gastrointestinal immature and adult roundworms.

Lung Worms : Both adult and Fourth - Stage larvae of Dictyocaulus viviparous.

Liver Flukes : Immature and adult Fasciola hepatica & Fasciolagigantica.

Eye Worm : Thelazia app.Ectoparasites (Dermatobiahominis, Psoroptesbovis) Including Sucking Lice, Ticks & Mites.

 

CONTRAINDICATION :

Administration to lactating animals and pregnant heifers within 60 days of Calving. This product is not for intravenous or intramuscular use.

 

DOSAGE AND ADMINISTRATION :

For subcutaneous administration.

General : 1.0 ml per 50 kg bodyweight

Cattle : 1 ml per 50 kg bodyweight

Sheep & Goat : 0.5 ml per 25 kg bodyweight

 

WITHDRAWAL PERIOD :

For meat : 35 days

 

PACK SIZE :

100 ml Vial

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Ivermectin And Closantel Injection (Vet) 100 ml Vial

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Ivermectin And Closantel Injection (Vet) 100 ml Vial
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COMPOSITION :

Each ml contains :

Closantel 125mg

Ivermectin B.P. 5mg

Propylene glycol B.P. q.s.

 

INDICATION :

For the treatment of mixed trematodes (fluke, amphistomes) and nematode or arthropod infestation due to gastrointestinal roundworms, lungworms, eyeworms, warbles, mites and lice of dairy animals.

 

CONTRAINDICATION :

Ivermectin and closantel injection is not for intravenous or intramuscular use.Do not in non-lactating dairy Cows including pregnant heifers within 60 days of Calving.

Does not use in cases of know hypersensitivity to the active ingridients.

 

DOSAGE AND ADMINISTRATION :

Ivermectin and Closantel injection should be administered at a dosage rate of 200mcg Ivermectin per kg bodyweight add 5 mg Closantel per kg bodyweight (1 ml per 25 kg) it should only be injected subcutaneously into the neck a. maximum dose of 10ml should administered at any one site with any residual volume administered at another site in the neck. A sterile 16-gauge One-inch needle is recommended. This product does not contain an antimicrobial preservative swab septum before removing each dose. Use a dry sterile needle and syringe. The timing for treatment should be based on epidemiological factors and should be customized for each individual farm. As with other anthelmintics, Veterinary advice should be on appropriate programs and stock to ensure administration of a correct dose. Bodyweight should be determined as accurately as possible; accuracy of the dosing device should be checked. If animals are be treated collectively rather than individually they should be

grouped according to their bodyweight and dose accordingly, in order to over-dosing.

 

Dose chart:

Body weight (kg) Dose (ml)by subcutaneous route

Upto 50 kg 2 ml

51-100 kg 4 ml

101-150 kg 6ml

151-200 kg 8 ml

201-250 kg 10 ml

251-300 kg 12 ml

301-350 kg 14 ml

351-400 kg 16 ml

401-450 kg 18 ml

More than 450 kg 20 ml

 

WITHDRAWAL PERIOD :

For meat : 35 days

 

PACK SIZE :

100 ml Vial

 

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Ivermectin Injection B.P. 1% (Vet)

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Ivermectin Injection B.P. 1% (Vet)
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COMPOSITION :

Each ml contains :

Ivermectin B.P.               10 mg

Benzyl Alcohol (as preservative)B.P.        1.5% v/v

Propylene Glycol B.P.         q.s.

 

INDICATION :

For treatment and control of gastrointestinal nematodes, Lung worms, Eye worms, Warbies and Ectoparasites like mites, ticks and lice in Cattle, Buffaloes, Horses, Sheep, Goats, Camels and Dogs.

 

CONTRAINDICATION :

I-TIN should not be used intravenously or intramuscularly. Do not use in lactating Cows or in dairy Cow during 28 days prior to calving.

 

DOSAGE AND ADMINISTRATION :

Cattle : Dosage : 1 ml per 50 kg bodyweight (based on a recommended level of 200 mcg Ivermectin per kg bodyweight).

Administration : Inject subcutaneously in front or behind the shoulder.

Swine : Dosage : 1 ml per 33 kg bodyweight (based on a recommended level of 303 mcg Ivermectin per kg bodyweight).

For the treatment of Psoroptes Ovis(mange mite), two injections with a seven day interval are required.

Administration : Inject subcutaneously into the neck A sterile 17 gauge 1/2 inch

needle in recommended.

 

WITHDRAWAL PERIOD :

Cattle : Must not be treated within 21 days of slaughter for human consumption. do not use in cattle producing milk for human Consumption or in dairy cows within 28 days prior to calving.

Swine : Must not be treated within 28 days of slaughter for human Consumption.

Sheep : must not be treated within 21 days of slaughter for human Consumption,

Do not treat lactating Cows or within 21 days before lambing where milk is to be used for human Consumption. 

 

PACK SIZE :

10 ml, 20 ml, 50 ml & 100 ml Vial.

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Ivermectin Injection B.P. 2% (Vet)

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COMPOSITION:

Each ml contains:

Ivermectin B.P.               20 mg

Benzyl Alcohol (as preservative) B.P.        1.5% v/v

Propylene Glycol B.P.         q.s.

 

For the treatment and control of internal & external Parasites of Cattle, Sheep, Deer, Goat, Camel & Dog.

 

DOSAGE AND ADMINISTRATION:

To be given subcutaneously cattle, sheep, dog & others small animals 0.5ml per 50 kg body weight.

Pig: 0.5 ml per 33 kg body weight.

 

WITHDRAWAL PERIOD:

Meat : Animal must not be staughtered after fast dose for human consumption.

Cattle:21 days

Sheep:35 days

Pigs:28 days

 

PACK SIZE:

100 ml Vial.

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Levamisole Injection 10% BP(Vet)

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Levamisole Injection 10% BP(Vet)
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COMPOSITION :

Each ml contains :

Levamisole Hydrochloride B.P.                 100 mg

Benzyl Alcohol B.P.                                 1.5% w/v

Water for injection B.P.                                    q.s.

 

INDICATION :

Levamisole is a broad spectum anthelmintic for use in the treatment and control of nematode infections in Cattle and Sheep.Lungworms : Dictyocaulus spp.

Gastro-intestinal worms : Trichostrogylus spp.Cooperi spp., Ostertagia spp., Haemonchus spp., Nematodirus  spp., Bunostomuum spp., Oesophagostomum spp., Chabertia spp.

 

CONTRAINDICATION :

It is safe for use in Cattle and Sheep at the recommended dosages. However, if the recommended dose rates are exceeded animals may exhibit signs of impaired motor function such as muscle tremors, head shaking and increased salivation which are of temporary nature. Although normally non-irritant, it may occasionally cause local reaction at the site of the injection; this should resolve naturally in a short period of time. Care should be taken to estimate accurately the bodyweight of animals to be treated before calculating the dosage. The product may be administered to pregnant or lactating animals but care should be taken when treating heavily pregnant animals or animals suffering stress from adverse weather conditions, poor nutrition, penning, handing etc.

 

DOSAGE AND ADMINISTRATION :

It should be administered by subcutaneous injection at a rate of 7.5 mg

levamisole hydrochloride per kg body weight.

Divide large dosage between two or more injection sites.

 

WITHDRAWAL PERIOD :

Animals must not be slaughtered for human consumption during treatment.

Cattle : Meat : 28 days

Sheep : Meat : 15 days

 

PACK SIZE :

30 ml, 50 ml, 100 ml Vial

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Levocarnitine Injection USP

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COMPOSITION :

Each ml contains :

Levocarnitine                BP           200mg

Water For Injection       BP               Q.S.

 

ACTION :

* Muscle levels of I-CARE determine the exercise capacity of muscles.

* I-CARE forms the essential transport system for use of fats as an energy source.

* I-CARE may help delay musccle fatigue and improve endurance.

* I-CARE is essential for normal heart function.

* Performance horses recover more effeciently when supplemented with I-CARE.

 

I-CARE is an amino acid which helps transport fats into muscle cells. I-CARE is essential in the transport of fats into muscle cells for production. The muscle levels of I-CARE 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. I-CARE delays muscle fatigue by reducing lactic acid formation, and improves performance and endurance. I-CARE 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 build-up in muscles, helping to delay fatigue and prevent Tying Up. Demand for I-CARE in heavily exercising horses is often not met from the diet, as large amounts are consumed during exercise. Supplementing with I-CARE results improved energy supply, increased use of fatty acids as an energy source, decreased lactate build-up, and a significant increase in maximum work output.

 

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 I-CARE by Intravenous Injection.

 

WITHDRAWAL PERIOD :

[Horses] : Nil

 

PACK SIZE :

100 ml Vial

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Meloxicam injection (Vet) 5 mg/ml

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Meloxicam injection (Vet) 5 mg/ml
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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.

 

INDICATION :

Dog: MELOXIN-I injection is indicated in Dogs for the control of pain and inflammation associated with osteoarthritis.

Cats: For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery.

Cattle: For the use in acute respiratory infection with appropriate antibiotic therapy to reduce clinical signs in Cattle. For use in diarrhoea 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 in the treatment of acute mastitis, in combination with antibiotic therapy.

Horse: 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 :

Carefully consider the potential benefits and risk of Meloxin-I & other treatment options before deciding to use MELOXIN-I. Use the lowest effective dose for the shortest duration consistent with individual response.

Dogs: It should be administered initially as a single dose at 0.02mg/kg bodyweight intravenously or subcutaneously, followed after 24 hours.

Cats: Administer a single, one-time subcutaneous dose of MELOXIN-I injection to Cats at a dose of 0.3mg/kg bodyweight. Use of additional Meloxicam Injection or other NSAIDs is contra indicated. To ensure accuracy of dosing, the use of a 1ml graduated syringe is recommended.

Cattle: Single subcutaneous or intravenous injection at a dosage of 0.5 mg meloxicam / kg bodyweight in combination with antibiotic therapy or with oral re-hydration therapy, as appropriate. The recommended maximum volume to be administered at a single injection site is 10 ml.

 

WITHDRAWAL PERIOD :

Cattle: Meat and offal:15 days Milk : 5 days

Horses & Swine: Meat and offal : 5 days

 

PACK SIZE :

30ml, 100 ml vial

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Nitroxynil 34% w/v injection B.P

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Description:

INITRO injection is orange to yellow colored liquid.

Each ml contains :

Nitroxynil 34% w/v with N-Ethyl D glucamine

 

INDICATION:

INITRO 34% injection is effective against:

- Liver fluke infestations caused by Fasciola hepatica and Fasciolagigantica.Gastrointestinal parasitism caused by Haemonchus,Oesophagostomum and Bunostomum in cattle,sheep and goats.

- Oestrusovis in sheep and camels

- Hookworms in dogs

 

DOSAGE AND ADMINISTRATION:

For subcutaneous

Cattle,sheep,goats,camels:1ml per 35 kg bodyweight by subcutaneous injection.

This dosage may be increased to 1.25 ml per 35 kg bodyweight in case of acute fascioliasis(immature flukes).

Dogs:0.30 ml per 10 kg bodyweight by subcutaneous injection.

 

PACK SIZE:

30ml,100 ml vial

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Oxytetracycline Hydrochloride Injection 10% w/v

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COMPOSITION :

Each ml contains :

Oxytetracycline Hydrochloride B.P.                100 mg

Propylene Glycol BP                                          q.s.

 

INDICATION :

The treatment of infections caused by bacteria sensitive to oxytetracycline in Horses, Cattle, Camel, Sheep, Goat, Dogs and Cats. In vitro, Oxytetracycline is active against range of both Gram-positive and Gram-negative microorganisms including Streptococcus spp., Staphyicocccus spp., Listeria monocytogenes, Mannheimia haemolytica, Haemophilus parahaemolyticus and Bordetellabronchiseptica.

 

CONTRAINDICATION :

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 animals : 3-10 mg oxytetracycline per kg bodyweight(depending on age and species-see table below)by intramuscular, subcutaneous or intravenous injection.

Small animals : 10 mg oxytetracycline per kg bodyweight by intramuscular or intravenous injection.

 

 

 

 

 

 

 

Maximum recommended dose at any one site : 20ml for Cattle, 10ml for Sheep. Clean the area of the injection site and swab with spirit. The treatment may be repeated at 24 hour intervals up 4 times(5 treatment in all).Intravenous injection must be given slowly over a period of at least one minute.

 

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 

 

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Oxytetracycline Hydrochloride Injection 5% w/v

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Oxytetracycline Hydrochloride Injection 5% w/v
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COMPOSITION :

Each ml contains :

Oxytetracycline Hydrochloride B.P. 50 mg

Propylene Glycol BP q.s.

 

INDICATION :

The treatment of infections caused by bacteria sensitive to oxytetracycline in Horses, Cattle, Camel, Sheep, Goat, Dogs and Cats. In vitro, Oxytetracycline is active against range of both Gram-positive and Gram-negative microorganisms including Streptococcus spp., Staphyicocccus spp., Listeria monocytogenes, Mannheima haemolytica, Haemophilus parahaemolyticus and Bordetellabronchiseptica.

CONTRAINDICATION :

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 tetracycline 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 animals : 3-10 mg oxy-tetracycline per kg bodyweight(depending on age and species-see table below)by intramuscular, subcutaneous or intravenous injection.

Small animals : 10 mg oxy-tetracycline per kg bodyweight by intramuscular or intravenous injection.

 

 

 

 

 

 

 

Maximum recommended dose at any one site : 20ml for Cattle, 10ml for Sheep. Clean the area of the injection site and swab with spirit. The treatment may be repeated at 24 hour intervals up 4 times(5 treatment in all).Intravenous injection must be given slowly over a period of at least one minute.

 

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

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Oxytetracycline Injection

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Oxytetracycline Injection
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Composition:

Each ml contains :

Oxytetracycline Dihydrate BP.

Equi to anhydrous Oxytetracycline 300 mg

In 2-Pyrrolidone vehicle system

 

Indication:

Beaf cattle,non-lactating dairy cattle,calves,including pre-ruminating(veal)calves:

Oxy 30% is indicated in the treatment of pneumonia and shipping fever complex associated with pasteurella spp., and histophilus spp. Oxy 30% is indicated for the treatment of infectious bovine keratoconjunctivitis(pink eye) caused by Moraxella bovis,foot-rot and diphtheria caused by fusobacterium necrophorum;Bacterial enteritis

(scours) caused by Escherichia coli;wooden tougue caused by actinobacillus lignieresi;Leptospirosis caused by leptospira Pomona;And wound infections and acute metritis caused by strains of staphylococcal and streptococcal organisms sensitive to Oxytetracycline.Also, it is indicated for the control of respiratory disease in cattle at high risk of developingbrd associated with mannheimia(pasteurella) haemolytica.

Swine:oxy 30% is indicated in the treatment of bacterialenteritis caused by Escherichia Coli;Pneumonia caused by pasteurella multocida;And leptospirosis caused by leptospira Pomona.

Dosage:

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.

 

Withdrawal Period:

21 days for meat and edible tissues;

7 days for milk.

Packaging:

100 ml vial

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Oxytetracycline Injection Long Acting 20% w/v

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Oxytetracycline Injection Long Acting 20% w/v
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COMPOSITION :

Each ml contains :

Oxytetracycline Dihydrate B.P. eq. to Anhydrous Oxytetracycline           200 mg

in 2-Pyrrolidone Vehicle system                                                                q.s.

 

INDICATION :

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 treatement 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 oxytetracycline sensitive organisms. This product may be used as an aid in the treatment of foot rot, acute, severe mastitis and infections ovine kerato conjunctivitis (pink-eye).

 

CONTRAINDICATION :

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 long acting effect, IMOLY 20% should be given by deep intramuscular injection at a rate of 20 mg equivalent of oxytetracycline base/kg body weight (i.e. 1ml IMOLY 20% per 10 kg body weight).In Cattle not more than 10 ml and in Sheep and Pigs not more than 5 ml to be given at any one site. In Pigs weighing less than 10 kg a maximum 1 ml dose should be used.

 

 

 

 

 

 

 

 

 

 

 

 

 

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.

 

PACK SIZE :

20ml, 50 ml, 100 ml Vial 

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Tylosin Injection B.P. 10% w/v(Vet.)

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Tylosin Injection B.P. 10% w/v(Vet.)
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COMPOSITION :

Each ml contains :

Tylosin tartate B.P.

equi. to tylosin base 100 mg

Benzyl Alcohol B.P. 2% v/v

Propylene glycol B.P.. and

Water for injection B.P. (1:1) q.s.

 

INDICATION :

Although the Injectable form of Tylosin is approved for use in Dogs and Cats, it

is rarely used parenterally in those species.Tylosin is also used clinically in

Cattle and Swine for infections caused by susceptible organisms.

Lungworms: Dictyocauius spp.

 

DOSAGE AND ADMINISTRATION :

Cattle :

For susceptible infections :

a) 17. 6 mg/kg IM once daily.Continue treatment for 24 hours after symptoms have stopped, not to exceed 5 days.Do not inject more than 10 ml per site.

Use the 50 mg/ml formulation in Calves weighing less than 200 pounds.

b) 5-10 mg/kg IM once daily;not to exceed 5 days.

c) Tylosin base injectable : 10 mg/kg IM initially, then 6 mg/kg IM q8h (q8-12h in Calves).

PACK SIZE :

30 ml, 50 ml, 100 ml Vial

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Tylosin Injection B.P. 20% w/v(Vet.) 200 mg/ml

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Tylosin Injection B.P. 20% w/v(Vet.) 200 mg/ml
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COMPOSITION :

Each ml contains :

Tylosin Base B.P. 200 mg

Benzyl alcohol B.P. 2% w/v

Propylene Glycol B.P. and

Water for Injection B.P.(1:1) q.s.

 

INDICATION :

Cattle : Tylosin Injection is indicated for use in the treatment of bovine respiratory complex (shipping fever, pneumonia) usually associated with Pasteurella multocida and Actinomyces pyogenes; foot rot (necrotic pododermatitis)and calf diphtheria caused by Fusobacierium necorphorum and metritis caused by Actinomyces pyogenes.

Sheep : Pneumonia, arthritis, contagious and acute agalaxia due Mycoplasma agalactie, mastitis.

Goat : Contagious pleuropneumonia due Mycoplasma mycoeides.

 

CONTRAINDICATION :

Not to be used in animals known to be hypersensitive to the active ingredient.

 

DOSAGE AND ADMINISTRATION :

Cattle :

Inject 5-10 mg/kg body weight daily Intramuscularly.

Do not inject more than 5 ml per Injection site.

Sheep and Goats:

Inject 10 mg/kg of body weight daily Intramuscularly.

Do not Inject more than 5 ml per Injection site.

 

WITHDRAWAL PERIOD :

Cattle :

Edible tissue - 7 days

Milk - 72 hours

Sheep, Goats :

Edible tissue - 7 days

Milk - 48 days

PACK SIZE :

100 ml Vial

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Vitamin A,D3,E Injection

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Vitamin A,D3,E Injection
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Description:

ELCINVIT is oily clear liquid injection containing

1. Vitamin A 2000 I.U.

2. Vitamin D3 2000 I.U. 

3. Vitamin E 4mg 

4. 4. Sesam oil q.s. 

Indications:

Treatment and prevention of vitamin deficiency in farm animals,such as growth disturbance,weakness of new-born animals,neonatal anemia,sight disturbance,intestinal trouble,convalescence,anorexia,not-infections reproductive disturbance,rechitis,muscle weakness,muscular tremor and myocardial failure withdifficulty in breathing;worm infection

Dosage:

1) For subcutaneous or intramuscular injection

2) Cattle : 10-20 ml per animal

3) Calves foal: 5-10 ml per animal

4) Lambs: 10 ml per animal

Packaging:

10 ml,100 ml vial

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Vitamin B Complex Injection

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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.

Indications:

Prevention and treatment of hypocalcaemia, debility, weakness, to

improve health , productivity and milk yield.

Dosage:

Intramuscular Injection

Horse Cattle : 10 - 20 ml

Sheep Swine : 2-6 ml

Dog,Cat Rabbit : 0.5-1 ml

Packaging:

100 ml vial

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Intracin Pharmaceuticals Pvt. Ltd.WHO GMP Accredited Company
Alfina Ansari (Marketing Manager)
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Nadiad - 387001, Gujarat, India
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