Intracin Pharmaceuticals Private Limited Kheda, Gujarat

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 inhorses, cattle, camel, sheep, goat, dogs and cats. in vitro, oxytetracycline isactive against a range of both gram-positive and gram-negativemicroorganisms including staphyicocccus spp., listeria monocytogenes, mannheimia haemolytica, haemophilus parahaemolyticus, bordetellabronchiseptica, and against chlamydophila abortus (formerly chlamydiapasittaci), 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 inhorses and subcutaneous administration in dogs.the use of tetracyclinesduring the period of tooth and bone development, including late pregnancy, may lead to discolouration.not to be used in sheep producing milk for humanconsumption.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 byim , iv or sc injection

small animal : 5-10 mg oxyteracycline per kg body weight for 3 to 5 days byim or iv injection

withdrawal period :

animal must not be slaughtered and milk should not be used for humanconsumption 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

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 tooxytetracycline.

cattle : for the treatment and control of pasteurellosis and pneumonia causedby oxytetracycline sensitive organisms and as an aid in the treatment ofinfectious bovine keratoconjunctivitis (new forest disease) due tooxytetracycline sensitive strains of moraxeila bovis. this product may also beof 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 byoxytetracyclinesensitive organisms. this product may be used as an aid in thetreatment of foot rot, acute, severe mastitis and infectious ovinekeratoconjuctivitis (pink-eye).

contra-indications :

not recommended for cats, dogs, horses and donkeys.

the use of this product during the period of tooth development including latepregnancy may lead to tooth discoloration.

dosage and administration :

i.m./subcutaneous use

deep intramuscular use only in large & small animals and subcutaneous inpoultry.

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

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

COMPOSITION :

Each ml contains :

Nitroxynil B.P 340 mg

Water for Injections B.P q.s.

INDICATIONS :

INITRO 34% Injection is effective against:

- Liver fluke infestations caused by Fasciola hepatica andFasciolagigantica. Gastrointestinal parasitism caused byHaemonchus, Oesophagostomum and Bunostomum in Cattle, Sheepand Goats.

- Oestrusovis in Sheep and Camels.

- Hookworms in Dogs.

CONTRA-INDICATIONS :

Do not use in animals with known hypersensitivity to the activeingredient.

Do not use in animals producing milk for human consumption. Do notexceed stated dose.

DOSAGE AND ADMINISTRATION :

For Subcutaneous Cattle, Sheep, Goats, Camels : 1ml per 35 kgbodyweight by Subcutaneous Injection.This dosage may be increasedto 1.25 ml per 35 kg bodyweight in case of acute fascioliasis (immatureflukes).

Dogs : 0.30 ml per 10 kg bodyweight by Subcutaneous Injection.

WITHDRAWAL PERIOD :

Withdrawal times :

For meat :

Cattle : 60 days.

Sheep : 49 days.

PACK SIZE :

50 ml, 100 ml Vial

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 mostspecies. it is often used in settings where gentamicin-resistant bacteria are aclinical problem. the inherent toxicity of the aminoglycosides limit theirsystemic use to serious infections when there is either a documented lack ofsusceptibility to other less toxic antibiotics or when the clinical situation dictatesimmediate treatment of a presumed gram negative infection before culture andsusceptibility results are reported. amikacin is also approved for intrauterineinfusion in mares.

contra-indications :

aminoglycosides are contraindicated in patients who are hypersensitive tothem. because these drugs are often the only effective agents in severegramnegative infections there are no other absolute contraindications to theiruse. however, they should be used with extreme caution in patients withpreexisting renal disease with concomitant monitoring and dosage intervaladjustments made. other risk factors for the development of toxicity includeage (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

composition :

each ml contains :

chlorphenamine maleate b.p 10 mg

phenyl mercuric nitrate b.p 0.002 % w/v

(as preservative)

water for injections b.p q.s.

indications :

1. allergic reactions and allergic disorders with manifestation of acuterespiratory signs.

2. rhinitis, dyspnoea, pulmonary emphysema, pulmonary oedema, asthma and hay fever.

3. eczema, dermatitis, urticaria, insect bite, tail eczema in horses, toxichoof corn

4. ruminal atony, tympany and bloat in ruminant.

5. puerperal toxaemia and secondary placental retention, acute septicmetritis 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 byveterinarian.

withdrawal period :

nil

pack size :

30 ml, 100 ml vial

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

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 andinflammation associated with musculoskeletal disorders.

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

DOSAGE AND ADMINISTRATION :

Cattle : The recommended dose is 2.2 mg/kg for the antipyretic effect in acuteinflammatory conditions in Cattle. Intravenous administration is recommended.

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

Horses : The recommended dose for musculoskeletal disorders in Horses is1.1 mg per kg of bodyweight once daily. Treatment may be given byIntravenous or Intramuscular Injection and repeated for up to five days.Studies show that onset of activity is within two hours. Peak response occursbetween 12 and 16 hours and duration of activity is 24-36 hours. Therecommended dose for the alleviation of pain associated with equine colic is1.1 mg per kg of bodyweight.

Intravenous administration is recommended for prompt relief. Clinical studiesshow pain is alleviated in less than 15 minutes in many cases. Treatment maybe repeated when signs of colic recur. During clinical studies approximately10% of the Horses required one or two additional treatments. The cause ofcolic should be determined and treated with concomitant therapy.

WITHDRAWAL PERIOD :

Cattle : Meat : 7 days

Milk : 36 days

Horses : Meat : 7 days

All target species : 22 days

PACK SIZE :

50 ml, 100 ml Vial

COMPOSITION :

Each ml contains :

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, Sheepand Pigs caused by or associated with organisms sensitive to Oxytetracycline.

For the treatment and control of pasteurellosis and pneumonia caused byoxytetracycline sensitive organisms and as an aid in the treatment of infectiousbovine keratoconjunctivitis (New Forest Disease) due to oxytetracyclinesensitive strains of Moraxeila bovis. This product may also be of value forfoul-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 latepregnancy 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 andmore than 5 ml in Calves, Goats and Sheep per Injection site.

WITHDRAWAL PERIOD :

Milk for human consumption should not be taken during treatment. Milkintended for human consumption may be taken only after 7 days from the lasttreatment. Not for use in ewes producing milk for human consumption. Animalsmay only be slaughtered for human consumption after last treatment, accordingto the below table.

Species Meat withdrawal periods

Cattle & Sheep 28 days

Pigs 35 days

PACK SIZE :

20 ml, 50 ml, 100 ml Vial