Veterinary Medicines

Allianox (Oral suspension. 1000 ML)

Under registration

Anti parasite

Effective  formula support cattle and sheep against internal parasite

Uses and Indications:

  • Allinox is effective in the treatment and control of roundworm, lungworm and fluke infections in cattle and sheep.
  • Allinox is effective against mature and developing immature stages of levamisole-susceptible major stomach and bowel worm species including Trichostrongylus spp, Cooperia spp, Ostertagia spp (except Ostertagia larvae in cattle), Haemonchus spp, Nematodirus spp, Bunostomum spp, Oesophagostomum spp, Chabertia spp and lungworms Dictyocaulus spp.
  • Allinox is effective against mature liverfluke in cattle and sheep  in cattle and sheep.

Dose:

1 ml/2 kg body weight orally

Composition

An aqueous suspension for oral administration. Each ml of allianox contains 22 mg of Rafoxanide and 15 mg of Levamisole Hydrochloride.

Contraindications

  • Do not use in animals with known hypersensitivity to the active ingredients. Do not use in animals less than 6 months of age.
  • Withdrawal period(s) Animals intended for human consumption must not be slaughtered during treatment. Cattle and sheep may be slaughtered for human consumption only after 60 days from the last treatment.
  • Cattle: Not authorised for use in cattle producing milk for human consumption including pregnant cattle intended to produce milk for human consumption.

Biofloxacin (injection vial)

Under registration

Antibiotic

A synthetic fluoroquinolone antimicrobial agent

Uses and Indications:

  • For the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica and Pasteurella multocida in beef cattle
  • for the control of BRD in beef cattle at high risk of developing BRD associated with Mannheimia haemolytica and Pasteurella multocida.

Dose:

  • Care should be taken to dose accurately. Administered dose volume should not exceed 15 mL per injection site.
  • Single-Dose Therapy (BRD Treatment and Control in Cattle at High Risk):
  • Administer subcutaneously at 8 mg/kg of body weight (2 mL/100 lb) as a one-time injection.
  • Multi-Day Therapy (BRD Treatment):Administer subcutaneously at 6 mg/kg of body weight (1.5 mL/100 lb) with this treatment repeated once approximately 48 hours following the first injection.

Composition

  • Sterile Injectable Solution Antimicrobial 180 mg of danofloxacin as the mesylate salt/mL For subcutaneous use in beef cattle.
  • Not for use in cattle intended for dairy production or in calves to be processed for veal.

HUMAN WARNINGS

  • For use in animals only.
  • Keep out of reach of children.
  • Avoid contact with eyes. In case of contact, immediately flush eyes with copious amounts of water for 15 minutes. In case of dermal contact, wash skin with soap and water.
  • Consult a physician if irritation persists following ocular or dermal exposures.
  • Individuals with a history of hypersensitivity to quinolones should avoid this product. In humans, there is a risk of user photosensitization within a few hours after excessive exposure to quinolones.

Gentaliance (injection vial)

Under registration

Antibiotic

a water soluble (bactericidal) antibiotic of the aminoglycoside group

Uses and Indications:

is clinically effective in infections due to susceptible gram-negative and gram-positive bacteria, including Pseudomonas aeruginosa, indole negative and indole positive Proteusspecies, Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes, Arizona hinshawii, and Staphylococcus species. The use of GENTOCIN injectable solution is indicated in the treatment of infections caused by laboratory determined susceptible bacteria, with due regard for relative antibiotic toxicity.

Composition

Gentamicin(sulfate) 80 mg

CONTRAINDICATIONS

  • Do not use in known cases of kidney dysfunction.
  • Do not use in case of hypersensitivity to the active substance or to any excipient.
  • Do not exceed the recommended dosage •
  • Do not use during pregnancy.
  • Do not use in dehydrated animals or with hearing alteration (loss of balance or inner ear damaged).
  • Use of gentamicin on foals and neonates is not recommended

Dose

INTRA-UTERINE:

a) Horses:0 – 2.5 grams once per day for three to five days during estrus. Each dose should be diluted with 200-500 mL sterile physiological saline before aseptic uterine infusion.

Although Gentaliance injectable solution is not spermicidal, treatment should not be given the day of breeding.

(b) Dogs: 4.4 mg/kg (2 mg/lb) body weight once a day for four days. Each dose should be diluted with 10 mL sterile physiological saline before aseptic uterine infusion.

(c) Cows: 200 mg one time only. The dose should be diluted with 16 mL sterile physiological saline solution before aseptic uterine infusion. Although Gentaliance injectable solution is not spermicidal, treatment should not be given the day of breeding.

INTRAMUSCULAR:

Dogs and Cats: 4.4 mg/kg (2 mg/lb) body weight twice the first day: 4.4 mg/kg (2 mg/lb) body weight once a day thereafter. Average duration of treatment in clinical studies was five to seven days.

Ordinarily, treatment should not be given for more than 7 to 10 days or be repeated unless required for serious infections not responsive to other agents.

SUBCUTANEOUS:

(a) Dogs and Cats: 4.4 mg/kg (2 mg/lb) body weight twice the first day: 4.4 mg/kg (2 mg/lb) body weight once a day thereafter. Average duration of treatment in clinical studies was five to seven days.

(b) Turkey Poults: Each turkey poult should be injected aseptically once subcutaneously in the neck with 1 mg of Gentaliance injectable solution. To prepare 50 mL of 5 mg/mL solution, dilute 2.5 mL of Gentaliance injectable solution 100 mg/mL with 47.5 mL of sterile physiological saline solution. Inject 0.2 mL per turkey poult.

(c) Chicks: Each one-day old chick should be injected aseptically once subcutaneously in the neck with Gentaliance injectable solution diluted with sterile physiological saline solution to provide 0.2 mg Gentaliance in a 0.2 mL dose.

How Supplied

Gentaliance injectable solution 80 mg/mL is packaged in 100 mL multiple dose vials containing 80 mg/mL of gentamicin base in an aqueous solution

Amoxizone 25% (powder)

Under registration

Moderate spectrum antibiotic

a water soluble (bactericidal) antibiotic of the penicillin group

Formula:

Every 100 g, it contains:
Amoxicillin (as trihydrate)………25 g
Formulation agents………………….q.s.

Indications:

Treatment of infections of the genito-urinary, respiratory and digestive systems.

Animal species to which it is intended:

Poultry.

Administration:

By oral route.

Dosage:

Poultry: 8 to 16 mg per k.l.w. per day. In the drinking water: 1 g every 1 liter of water.

Presentation:

Bag containing 1 kg.

Mectifluk 1% (injection)

Under registration

Injectable Solution controls more parasite species and larval stages than any other injectable parasite control product.

Formula:

Contain Dormectin 1% injectable solution for cattle 10 mg/mL

Indications:

  • For the treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs (see precautions), sucking lice and mange mites.
  • Consult your veterinarian for assistance in the diagnosis, treatment,
    and control of parasitism.

Animal species to which intended:

Cattle

Precautions

  • For subcutaneous or intramuscular injection in cattle only.
  • Residue warning: Do not slaughter for human consumption within 35 days of treatment.
  • A withdrawal period has not been established for this product in pre-ruminating calves.
  • Do not use in calves to be processed for veal.
  • Warning: Not for human use. Keep out of reach of children.

Administration:

By subcutaneous or intramuscular injection

Dosage:

  • Administer injectable solution at the recommended dosage of 200 mcg doramectin per kg (91 mcg/lb) of body weight. Each mL contains 10 mg of doramectin, sufficient to treat 110 lb (50 kg) of body weight.
  • Injections should be given using 16- to 18-gauge needles, regardless of administration route. Needles 1/2 to 3/4 inches in length are suggested for SC injections, which should be given under the loose skin in front of or behind the shoulder.
  • A 1 1/2-inch needle is suggested for IM injections. The only area for IM injections is the muscular region of the neck

Presentation:

100-mL, multi-dose, rubber-capped amber glass bottles contained in a clear polycarbonate shield.

Farmatyl  (powder)

Under registration

Antibiotic

Formula:

Contain Tylosin (as tylosin phosphate)  903 g Premix

Indications:

Beef Cattle:

To reduce the incidence of liver abscesses caused by Trueperella pyogenes (formerly Arcanobacterium pyogenes) and Fusobacterium necrophorum in beef cattle (steers and heifers) fed in confinement for slaughter.

 Broiler Chickens:

As an aid in the treatment of necrotic enteritis caused by Clostridium perfringens in broiler chickens.

Animal species to which it is intended:

Cattle, poultry

Administration:

Premix mixed in feeds

Dosage:

Broilers  200 gms per ton of feed (20 ppm) from day 1 till 45th day

Layers    500 gms per ton of feed (50 ppm) from point of lay till 42nd week & 200 gms per ton of feed (20ppm) from 43 week

Breeders   500 gms per ton of feed (50 ppm) from point of lay Or as recommended by the Nutritionist

Presentation:

1 kg

Neural 50% (WS powder)

Under registration

Neural is a broad-spectrum bactericidal aminoglycosidic antibiotic with particular activity against certain members of the Enterobacteriaceae e.g. Escherichia coli. Its mode of action is at the ribosomal level. When administered orally, only a fraction (<5%) is absorbed systemically, the remainder remains as the active compound in the gastro-intestinal tract of the animal. Neomycin is not inactivated by enzymes or food. These pharmacological properties lead to neomycin being an efficacious antibiotic in the prevention and treatment of enteric infections caused by bacteria sensitive to neomycin.

Formula:

1 gm Contain

Neomycin sulphate 500 mg

Indications:

Neoral-500 WS is indicated for the prevention and treatment of bacterial enteritis in calves, sheep, goats, swine and poultry caused by bacteria susceptible to neomycin, such as E. coli, Salmonella and Campylobacter spp.

Animal species to which it is intended:

Cattle, poultry

Administration:

Drinking water

Dosage:

For oral administration:

  • Calves, goats and sheep:
    10 mg neomycin sulphate per kg body weight (equivalent to 14 mg/kg) for 3 – 5 days.
  • Poultry:
    300 g per 2000 liters of drinking water for 3 – 5 days.

Presentation:

Sachet of 100 g and jar of 1000 g.

Floroliance (injection)

Under registration

Antibiotic and anti-inflammatory

  • Floroliance is an injectable solution of the synthetic antibiotic florfenicol and the non-steroidal anti-inflammatory drug (NSAID) flunixin.
  • Floroliance (florfenicol and flunixin meglumine) is a simple bovine respiratory disease (BRD) treatment strategy.
  • It involves a combination of two therapies in one dose: the powerful antibiotic florfenicol to kill or inhibit the disease-causing bacteria  and, the fast-acting non-steroidal anti-inflammatory drug (NSAID) flunixin meglumine to reduce BRD-associated fever.

Formula

Each milliliter of sterile floroliance contains 300mg florfenicol, 16.5mg flunixin as flunixin meglumine, 300mg 2-pyrrolidone, 35mg malic acid, and triacetin qs.

Indications:

Floroliance  is indicated for treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis, and control of BRD-associated pyrexia in beef and non-lactating dairy cattle.

Administration and Dosage

  • A single subcutaneous dosage of 6 mL/hundred pounds can produce improvement in just six hours.
  • Floroliance should be administered once by subcutaneous injection at a dose rate of 40mg florfenicol/kg body weight and 2.2mg flunixin/kg body weight
  • Do not administer more than 10 mL at each site.
  • The injection should be given only in the neck.

Presentation:

100mL Multiple-Dose Vial

Animal species to which it is intended:

Beef and non-lactating dairy cattle

Phenyloflam  (injection)

Under registration

Anti-inflammatory, non steroidal; analgesic; antipyretic.

A unique combination to relieve the pain, fever and swelling

Formula

Each ml contains:

Phenylbuatzone 200 mg

Sodium Salicylate 5 mg

Indications:

  • A unique combination to relieve the pain, fever and swelling.
  • it is indicated in Myositis, Laminitis , Neuritis and other such inflammatory conditions.
  • It is useful in the treatment of non visceral trauma, pain, Lameness, Swelling and pyrexia.
  • Relief of inflammatory conditions associated with the musculoskeletal system is a common labeled indication for the use of phenylbutazone in dogs and horses.
  • Phenylbutazone is indicated for the relief of musculoskeletal inflammation and mild to moderate somatic or pain

Administration and Dosage

By deep I/M only.

Large Animals:  10 – 15 ml
Small Animals:  1-2 ml

Presentation:

100 mL Multiple-Dose Vial

Animal species to which it is intended:

Dog, horses and cattle

Volaflam 5% (injection)

Under registration

Anti-inflammatory

Formula

Diclofenac sodium 5 g, excipient q.s.100ml

Indications:

Diclofenac sodium is a non steroidal anti-inflammatory drug derived from phenylacetate. Used for the treatment of arthritis rheumatism and muscle aches. Reduces fever caused by types of bacteria, virus and some other factors. 

Administration and Dosage

Intra-muscular injection
Dosage: once a day, for 2 to 3 days in succession.
Cattle: 2.5mg/kg weight,   ie 5ml for 100kg
Sheep and goats: 2.5mg/kg weight,  ie 1.5ml for 30kg

Presentation:

100mL Multiple-Dose Vial

Animal species to which it is intended:

Cattle, sheep, goats and dogs

Xinamycin (injection)

Under registration

Antibiotic

Antibacterial with bactericidal activity (group of aminoglycosides)

Formula

  • Powder for injection, vial containing 1 g of streptomycin base, to be dissolved in 4 ml of water for injection, for IM injection.
  • DO NOT ADMINISTER BY IV INJECTION.

Indications:

For treatment of diseases caused by bacteria susceptible to streptomycin

Cattle, Horses : Bacterial pneumonia

Dogs : Purulent disease

DOSAGE AND USE

Inject intramuscularly as Follows per 10kg of body weight once a day at intervals of 2~3days

Cattle, Horse, Calves: 0.5mL

Small animals: 0.5 ~ 1.0mL

Presentation:

100mL Multiple-Dose Vial

Animal species to which it is intended:

Cattle, sheep, goats and dogs, poultry

Alliacloxal (powder)

Under registration

Antibiotic

Broad bactericidal activity in fighting Infections and counteracts Beta-lactamase producing organisms.

Alliacloxal exerts superior bactericidal effect offers higher serum concentrations, acid stable and is rapidly and more completely absorbed, even in the presence of feed than Ampicillin.

Alliacloxal is a bactericidal providing superior action, effective against gram negative aerobic bacteria and offers complete absorption from GL tract even in the presence of Calcium, Magnesium and Iron salts unlike Tetracyclines.

Formula

Amoxicillin Trihydrate I.P.
equivalent to amoxicillin : 10% W/W

Cloxacillin Sodium I.P.
equivalent to Cloxacillin :10% W/W

Indications:

Treatment of:

Chronic Respiratory Disease Complex
Infectious Coryza
Early Chick Mortality
Wing Rot
Fowl Typhoid
Colisepticaemia
Pullorum Disease
Nonspecific diarrhea
Secondary Bacterial Infections
Stress and Laying Slumps

DOSAGE AND USE

1.0 gm / 4 litres of drinking water for 3 to 5 days.

Presentation:

Sachet of 100 g and jar of 1000 g.

Animal species to which it is intended:

poultry

Alliamikana (injection)

Under registration

Antibiotic

Injectable antibiotic that contains kanamycin sulfate, an aminoglycoside antibiotic, as an active ingredient. Kanamycin sulfate shows bactericidal activity against Gram-positive bacteria, Gram-negative bacteria, acid-fast bacilli, and others.

Formula

Powder for injection, vial containing kanamycin sulphate 150000 IU

Indications:

Cattle: pneumonia, bronchitis, bacterial diarrhea, bacterial arthritis, mastitis
Swine: pneumonia, bacterial diarrhea
Chickens: colibacillosis

DOSAGE AND USE

Intramuscularly administer the following dosage of kanamycin per kilogram body weight once daily.

Cattle: 5-10 mg (potency) [0.05-0.1 mL of the product]
Swine: 10-20 mg (potency) [0.1-0.2 mL of the product]
Chickens: 25-50 mg (potency) [0.25-0.5 mL of the product]

Presentation:

100mL Multiple-Dose Vial

Animal species to which it is intended:

Cattle, sheep, goats and poultry

Alliaprimital (powder)

Under registration

The combination of trimethoprim and sulfadiazine acts synergistic and usually bactericidal against many Gram-positive and Gram-negative bacteria like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp. Both compounds affect bacterial purine synthesis in a different way, as a result of which a double blockade is accomplished.

Formula

Contains per ml:

Sulfadiazine 500 mg.
Trimethoprim 100 mg

Indications:

Gastrointestinal and respiratory infections caused by trimethoprim and sulfadiazine sensitive micro-organisms, like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp. in calves, sheep, goats, poultry .

DOSAGE AND USE

For oral administration: Calves, goats and sheep : Twice daily 5 ml per 100 kg body weight for 4 – 7 days. Poultry : 1 litre per 1500 – 2500 litres of drinking water for 4 – 7 days.

Note: for pre-ruminant calves, lambs and kids only. Shake well before use.

Presentation:

Sachet of 100 g and jar of 1000 g.

Animal species to which it is intended:

Cattle, sheep, goats and poultry

Alliatulafen (injection)

Under registration

Antibiotic and non-steroidal antiinflammatory

Injectable Solution is a ready to use sterile parenteral preparation containing tulathromycin, a semi- synthetic macrolide antibiotic of the subclass triamilide and ketoprofen a non-steroidal anti-inflammatory drug

Formula

Tulathromycin 100 mg
Ketoprofen 120 mg

Indications:

Treatment of bovine respiratory disease (BRD) associated with pyrexia due to Mannheimia
haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis susceptible to
tulathromycin.

DOSAGE AND USE

Subcutaneous use.
A single subcutaneous injection of 2.5 mg tulathromycin/kg bodyweight and 3 mg
ketoprofen/kg bodyweight (equivalent to 1 ml/40 kg bodyweight). For treatment of cattle over
400 kg bodyweight, divide the dose so that no more than. 10 ml are injected at one site.

Presentation:

100mL Multiple-Dose Vial

Animal species to which it is intended:

Cattle, sheep, goats