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


Veterinary Injectable 2

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.


Amikacin Injection BP 250 mg/ml

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Amikacin Injection BP 250 mg/ml
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COMPOSITION :

Each ml contains :

Amikacin Sulphate B.P.

Equivalent to Amikacin base                      250 mg

Methyl hydroxyl benzoate B.P.              0.18% w/v

Propyl Hydroxy benzoate B.P.             0.025% w/v

Water for Injection B.P.                                    q.s.

 

INDICATION :

While parenteral use is only approved in Dogs, 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.

 

CONTRAINDICATION :

Aminoglycosides are contraindicated in patients who are hypersensitive to them. Because these drugs are often the only effective agents in severe gram-negative infections there are no other absolute contraindications to their use. However, they should be used with extreme caution in patients with pre-existing 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 :

As directed by the veterinary physician. Administered by Intramuscular and intravenous use only.

 

WITHDRAWAL PERIOD :

Eggs : 7 days

Meat : 28 days

 

PACK SIZE :

10 ml, 50 ml & 100 ml Vial

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Benzyl Penicillin for Injection B.P.

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Benzyl Penicillin for Injection B.P.
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COMPOSITION :

Each ml contains :

1. Each Vial contains :

    Benzylpenicillin Sodium B.P. equi. to Benzyl Penicillin       5000000 I.U.(3000 mg)

    Buffering Agent : Anhydrous sodium Citrate U.S.P.

2. Sterile Water for Injection I.P. 15 ml 1-Ampoule

 

INDICATION :

TWIN-PGS is used in treatment of mastitis, metritis, actinomycosis, anthrax, black leg, tetanus, haemorrhagic septicaemia in Cattle; Strangles, corynebacterial pneumonia in foals, tetanus in horses; Erycephalus in Pigs; Tetanus, foot rot, malignant oedema in Sheep and Goat; Rickettsiosis, tetanus and wound infection in dogs.

 

CONTRAINDICATION :

Do not use in animals with a known hypersensitivity reaction to any of the penicillins. TWIN-PGS should not be used in Cats, Rabbits, Guinea Pigs, Hamsters, Gerbils or other similar small animals.

 

DOSAGE AND ADMINISTRATION :

Cats and Dogs : Intramuscular 20, 000to 40, 000 I.U. per kg of bodyweight every six to eight hours.

Horses : Intramuscular 20, 000 I.U. per kg of bodyweight every six to eight hours.

 

WITHDRAWAL PERIOD :

Calves, Preruminating : Meat : 7 days

Cattle : Meat : 4 days, Milk : 48 hours

Sheep : Meat 6 days

Pigs : Meat : 6 days

Animal must not be slaughtered and milk may not be used for human consumption during treatment.

 

PACK SIZE :

20 ml Vial containing 3 gm of powder

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Ceftriaxone Sodium Injection B.P. 3g/Vial (Vet)

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Ceftriaxone Sodium Injection B.P. 3g/Vial (Vet)
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COMPOSITION :

Each vial contains :

Ceftriaxone Sodium BP

equi. to Ceftriaxone anhydrous             3g

 

INDICATION :

For the treatment of mastitis, resoiratory tract infection, skin and soft tissue infection.

 

CONTRAINDICATION :

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 :

Large Animals : 5-10 mg/kg. wt. twice or once daily by I.M./I.V. route.

 

WITHDRAWAL PERIOD :

Milk : 7 days

Meat : 28 days

 

PACK SIZE :

3 gm in 20 ml Vial

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Detomidine Hydrochloride Injection

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Detomidine Hydrochloride Injection
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COMPOSITION :

Each ml contains :

Detomidine Hydrochloride       BP      10 mg

Water For Injection                  BP         Q.S.       

 

ACTION :

Detomidine is a non-narcotic analgesic, and muscle relaxant, with a rapid dose-dependent effect. Sedation may be expected within 1-5 minutes following intravenous injection (slightly longer following intramuscular administration). T-DIN is an alpha-2 adrenocceptor agonist at central and peripheral sites. Its central depressive action produces sedation without any hypnotic effect. T-DIN produces analgesia by inhibition of CNS-mediated transmission of pain impulses and pain sensation. Full analgesic effect is expected 5-15 minutes after administration. A period of sedation is maintained for 0.5-6 hours, depending on the dose rate given. 

 

DOSAGE AND ADMINISTRATION :

TDIN can be given either Intravenously or Intramuscularly, as required. The effect is dose-dependent. The following scale can be used as a guide :

 

 

 

 

 

 

 

 

 

 

 

WITHDRAWAL PERIOD :

Not to be used in horses that may be slaughtered for human consumption. For analgesia in cases of spasmodic colic, give: 0.2 - 0.4 ml/100kg(0.02-0.04 mg/kg).This table should be considered as a base from which dosage can be modified to effect, according to the depth and duration of analgesia or sedation required. Do not store at low temperatures. Any unused portion should be discarded 3 months after first broaching vial. 

 

PACK SIZE :

1 litre

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Injection of Methylcobalamin, Vitamin B6

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Injection of Methylcobalamin, Vitamin B6
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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.

 

INDICATION :

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

 

WITHDRAWAL PERIOD :

Milk : Nil,Meat : Nil

 

PACK SIZE :

100 ml vial

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Meloxicam injection B.P. Vet 20 mg/ml

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Meloxicam injection B.P. Vet 20 mg/ml
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COMPOSITION :

Each ml contains :

Meloxicam B.P.                            20 mg

Benzyl alcohol B.P.                    2% v/v

Water for injection B.P.                   q.s.

 

INDICATION :

Meloxin-20 injection is indicated for anti-inflammatory & anti-pyretic purpose and the alleviation of pain in cattle

 

CONTRAINDICATION :

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 

 

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Parvaquone and Furosemide injection

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Parvaquone and Furosemide injection
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COMPOSITION :

Each ml contains :

Parvaquone                                                     150 mg

Furosemide  BP                                                 55 mg

Sorbitan mono oleate  BP   100 mg ( as preservative )

Oil base                                                                 Q.S 

 

CONTRAINDICATION :

East Coast Fever (ECF) is an immune-depressive disease and potentially fatal concurrent infections are common. In particular, anaplasmosis may be activated from the camet state and the principal lesions of ECF, such as oedema of the lungs and the alimentary canal, predispose to bacterial pneumonia and enteritis. The symptoms of these conditions may be masked by those of ECF. Special care should be taken to diagnose any complicating conditions and to treat them promptly and specifically.

 

DOSAGE AND ADMINISTRATION :

Inject by the intramuscular route into the neck muscles at the rate of 1ml/15kg (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 : 1ml per 15 kg body weight  

WITHDRAWAL PERIOD :

Milk : 14 days

Meat : 28 days

PACK SIZE :

50 ml, 100 ml Vial

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Parvaquone and Furosemide injection

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Parvaquone and Furosemide injection
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COMPOSITION :

Each ml contains :

Ketoprofen                        100 mg

Benzyl Alcohol B.P.           1%w/v

Water For Injection B.P.         q.s.

 

INDICATION :

Horse : Diseases affecting the osteoarticular and muscular-skeletal system associated with acute pain and inflammation: Lameness of traumatic origin, Naviculitis, Arthritis, Laminitis, Osteitis, spavin, Myositis Tendinitis, burstis. Ketoprofen is also indicated for post-surgical inflammation, symptomatic therapy of colic and fever.

 

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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Parvaquone injection 150 mg/ml(Vet)

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Parvaquone injection 150 mg/ml(Vet)
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COMPOSITION :

Each ml contains :

Parvaquone                              150 mg

Sorbitan mono oleate B.P.        100 mg

(as preservative)

Oil base                                          q.s.

 

INDICATION :

East Coast Fever 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.

 

CONTRAINDICATION :

Parvaquone shows no any side effects with any other commonly used veterinary products.

 

DOSAGE AND ADMINISTRATION :

Intramuscular route into the neck muscles.

Calves: 1ml per 50 kg

 

                    Body Weight                            Dose

                           100 kg                                   7 ml

                           150 kg                                 10 ml

                           200 kg                                 14 ml

                           250 kg                                 17 ml

                           300 kg                                 20 ml

 

WITHDRAWAL PERIOD :

Milk : 14 days

Meat : 28 days

 

PACK SIZE :

50 ml, 100 ml Vial

 

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Sodium Acid Phosphate With Vitamin B12 Injection

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Sodium Acid Phosphate With Vitamin B12 Injection
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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.

 

 

INDICATION:

It is indicated for infertility cases such as under developed ,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 turnover 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 sppetite 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.

 

PACK SIZE:

100 ml vial

 

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Strepto-Penicillin for Suspension Injection

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Strepto-Penicillin for Suspension Injection
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Composition:

Each vial of Dicrysticin-S contains:

Streptomycin Sulphate I.P.                                         2.5g

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

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

 

INDICATION:

Mixed bacterial infections caused by penicillin and streptomycin sensitive organisms.Infections in which the organisms cannot be readily identified.

 

DOSAGE AND ADMINISTRATION:

Large animals: 2ml per 50 kg bodyweight intramuscular

Small animals:1 ml per 5 kg bodyweight intramuscular

 

PACK SIZE:

2.5 g vial

 

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Strepto-Penicillin for Suspension Injection

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Strepto-Penicillin for Suspension Injection
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Composition:

Each vial of Dicrysticin-S contains:

Streptomycin Sulphate I.P.                                         5.0g

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

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

 

INDICATION:

Mixed bacterial infections caused by penicillin and streptomycin sensitive organisms.Infections in which the organisms can not be readily identified.

 

DOSAGE AND ADMINISTRATION:

Large animals: 2ml per 50 kg bodyweight intramuscular

Small animals:1 ml per 5 kg bodyweight intramuscular

 

PACK SIZE:

5 g vial

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Sulfadimidine Injection B.P. 33.3%

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Sulfadimidine Injection B.P. 33.3%
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COMPOSITION :

Each ml contains :

Sulfadimidine sodium    B.P.          333 mg

Benzyl alcohol               B.P.           1% v/v

Water for Injection         B.P.                q.s.

 

INDICATION :

SD-VET is indicated for pneumonia, foot rot, diphtheria in Calves, actinobacillosis, coli-bacillosis, salmonellosis, pasteurellosis, enteritis, poly-arthritis, streptococcal mastitis, dysentery, lymphangitis, young’s septicaemia and coccidiosis in Sheep and Goat, Cattle and Calves, For treatment of respiratory, lymphangitis, young’s septicaemia and coccidiosis in Sheep and Goat, Cattle and Calves. For treatment of respiratory and coccidosis infections in Poultry and Pigs.

 

CONTRAINDICATION :

Contraindicated in known cases of hypersensitivity to sulphonamides and in animals with severe liver damage or blood dyscrasias.

 

DOSAGE AND ADMINISTRATION :

For subcutaneous and slow intravenous administration.

Cattle : 3-6 ml.per 10 kg. body weight on the first day, followed by 3 ml per 10 kg. body weight on following 2-5 days.

Pigs : 50 mg per kg body weight during 3-7 days.

Poultry : 100 mg per kg body weight during 3 days.

In cold weather the solution may deposit fine crystals. This will re-dissolved on gentle warming.

 

WITHDRAWAL PERIOD :

Cattle, Sheep, Goat & Poultry : Meat : 18 days.

Cattle : Milk : 6.5 days.

Not for use in Sheep producing milk for human consumption.

Pigs : Meat : 42 days.

 

PACK SIZE :

100 ml Vial

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Thiamine Injection B.P.

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Thiamine Injection B.P.
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COMPOSITION :

Each ml contains :

Thiamine hydrochloride        BP         125 mg

Water For Injections              BP             Q.S.    

 

ACTION :

THIACIN injection provides the essential vitamin Thiamine. THIACIN  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 cannot 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. Never cells are particularly dependant on carbohydrate metabolism, and normal never function is greatly affected by increased levels of these acids during hard work.

 

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 :

1 litre

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Vitamin E/Selenium

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Vitamin E/Selenium
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COMPOSITION:

Each ml contains:

Vitamin E acetate                   70 mg

Selenium                               110 mg

Benzyl alcohol B.P.               2% v/v

Water for injection B.P.               q.s.

 

DOSAGE AND ADMINISTRATION :

As directed by veterinarian practitioners

 

INDICATION :

Depending on the actual product and species,Vitamin E/selenium is indicated for the treatment or prophylaxis of selenium-tocopheral deficiency(STD) syndromes in ewes and lambs(white muscle disease),sows,weanling and baby pigs(hepatic necrosis,mulberry heart disease),calves and breeding cows(White muscle disease),and horses(myositis associated with STD).A vitamin E/selenium product is also indicated for the adjunctive treatment of acute symptoms of arthritic conditions in dogs,but its efficacy for this indication has been questioned.

 

CONTRAINDICATION :

Vitamin E/selenium products should only be used in the species in which they are approved.Because selenium can be extremely toxic,the use of these products promiscuously cannot be condoned.When administering intravenously to horses,give slowly.

 

PACK SIZE :

100 ml vial

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Intracin Pharmaceuticals Pvt. Ltd.WHO GMP Accredited Company
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Nadiad - 387001, Gujarat, India
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Intracin Pharmaceuticals Pvt. Ltd.WHO GMP Accredited Company