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Alamycin 20 LA - 100ml

105690
A long acting broad spectrum injectable antibiotic containing Oxytetracycline Dihydrate equivalent to 200 mg/ml of Oxytetracycline base. It is suitable for acute infections caused by organisms sensitive to oxytetracycline. Blood levels persist for at least 4 days. Indicated for use in cattle, sheep and pigs in the treatment of: atrophic rhinitis caused by Bordetella bronchiseptica, Pasteurella haemolytica and Pasteurella multocida; navel/joint ill caused by Corynebacterium pyogenes, E. coli, and Staphylococcus aureus; mastitis caused by Corynebacterium pyogenes, E. coli, Staphylococcus aureus, Streptococcus agalactiae, and Streptococcus uberis; metritis caused by E. coli and Streptococcus pyogenes; pasteurellosis and infections of the respiratory tract caused by Pasteurella haemolytica and Pasteurella multocida; septicaemia caused by Salmonella dublin and Streptococcus pyogenes; erysipelas caused by Erysipelothrix rhusiopathiae. Alamycin LA can also be used in the control of enzootic abortion in sheep. The recommended dosage rate is 20 mg/kg bodyweight (1 ml per 10 kg bodyweight) by deep intramuscular injection. The product is recommended for a single administration only. Maximum recommended dose at any one site: Cattle 20ml Pigs 10ml Sheep 5ml Piglets: 1 day 0.2ml 7 days 0.3ml 14 days 0.4ml 21 days 0.5ml over 21 days 1.0ml/10kg Withdrawals Cattle: Meat 41 days,Milk 8 days Sheep: Meat 24 days, Milk 7 days Pigs: Meat 20 days

Alamycin L.A. 300 - 100ml

104340
For the treatment and control of a wide range of common systemic, respiratory, urinary and local infections caused by oxytetracycline sensitive organisms. Specific indications for Alamycin LA 300 Solution for Injection 300mg/ml would therefore include: pasteurellosis, pneumonia, atrophic rhinitis, erysipelas, joint ill/navel ill, summer mastitis in cows, ovine keratoconjunctivitis (pinkeye) and the control of enzootic abortion in sheep. Administer by deep intramuscular injection to cattle, sheep and pigs. 300mg/ml can be administered at the standard dose of 20mg/kg in order to obtain 3 to 4 days duration of activity or at the high dose of 30mg/kg for prolonged duration of activity (i.e. activity maintained for 5 to 6 days). Withdrawals Meat: Animals must not be slaughtered for human consumption during treatment. 20mg/kg dose: Cattle and sheep may be slaughtered for human consumption only after 28 days from the last treatment. Pigs may be slaughtered for human consumption only after 14 days from the last treatment. 30mg/kg dose: Cattle may be slaughtered for human consumption only after 35 days from the last treatment. Sheep and pigs may be slaughtered for human consumption only after 28 days from the last treatment. Milk: Milk for human consumption must not be taken during treatment. Milk for human consumption may be taken from cows only after 8 days from the last treatment. Milk for human consumption may be taken from ewes only after 8 days from the last treatment.

Alamycin L.A. 300 - 250ml

112851
For the treatment and control of a wide range of common systemic, respiratory, urinary and local infections caused by oxytetracycline sensitive organisms. Specific indications for Alamycin LA 300 Solution for Injection 300mg/ml would therefore include: pasteurellosis, pneumonia, atrophic rhinitis, erysipelas, joint ill/navel ill, summer mastitis in cows, ovine keratoconjunctivitis (pinkeye) and the control of enzootic abortion in sheep. Administer by deep intramuscular injection to cattle, sheep and pigs. 300mg/ml can be administered at the standard dose of 20mg/kg in order to obtain 3 to 4 days duration of activity or at the high dose of 30mg/kg for prolonged duration of activity (i.e. activity maintained for 5 to 6 days). Withdrawals Meat: Animals must not be slaughtered for human consumption during treatment. 20mg/kg dose: Cattle and sheep may be slaughtered for human consumption only after 28 days from the last treatment. Pigs may be slaughtered for human consumption only after 14 days from the last treatment. 30mg/kg dose: Cattle may be slaughtered for human consumption only after 35 days from the last treatment. Sheep and pigs may be slaughtered for human consumption only after 28 days from the last treatment. Milk: Milk for human consumption must not be taken during treatment. Milk for human consumption may be taken from cows only after 8 days from the last treatment. Milk for human consumption may be taken from ewes only after 8 days from the last treatment.

Aquaprim - 100ml

102001
Aquaprim is a broad spectrum antibacterial combination product containing two active substances: Trimethoprim 40mg/ml and Sulphadiazine 200 mg/ml. It is used for the treatment of disease caused by gram positive and gram negative micro-organisms sensitive to this combination. Species: Cattle and Pigs Dose: 12 ml per 100kg bodyweight daily for three consecutive days Calf 6.0 ml per 50 kg Cattle 12 ml per 100 kg Maximum volume at any one site of injection for cattle is 20 ml Piglet 0.6 ml per 5 kg Weaner 2.4 ml per 20 kg Fattner/Sow 9.0 ml per 75 kg Maximum volume at any one site of injection for a pig is 10ml Administration: For Intramuscular use only Withdrawal Meat and Offal: 25 days after last treatment. Milk: Not to be used for human consumption during treatment or for 72 hours (3 days) thereafter.

Baytril 100mg - 100ml

132050
Contains enrofloxacin, a fluoroquinolone. Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly to other classes of antimicrobials. Wherever possible, fluoroquinolones should only be used based on susceptibility testing. Cattle Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and secondary bacterial infections subsequent to viral infections (e.g. viral pneumonia) where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice. Treatment of local signs (inflammation, milk quality and yield) associated with peracute/acute mastitis in lactating dairy cattle caused by E. coli, where herd history and previous sensitivity testing indicate enrofloxacin as the drug of choice. Pigs Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis), and multifactorial diseases such as atrophic rhinitis and enzootic pneumonia, where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice. Dosage & Administration Cattle For respiratory and alimentary infections in cattle and secondary bacterial infections: administer by subcutaneous injection. 2.5 mg enrofloxacin per kg bodyweight daily by subcutaneous injection for 3 days (2.5 ml per 100 kg bodyweight) This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for salmonellosis and complicated respiratory disease. Not more than 10 ml should be administered at any one subcutaneous injection site. For E. coli mastitis: administer by slow intravenous injection. 5.0 ml per 100 kg bodyweight (5 mg enrofloxacin per kg bodyweight) daily for 2 days. Pigs For respiratory and alimentary infections in pigs and secondary bacterial infections: administer by intramuscular injection. 2.5 mg enrofloxacin per kg bodyweight daily by intramuscular injection for 3 days (2.5 ml per 100 kg bodyweight). This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for salmonellosis and complicated respiratory disease. Not more than 2.5 ml should be administered at any one intramuscular injection site in store pigs or 5 ml at any one intramuscular injection site in sows. Withdrawals Cattle: Subcutaneous Use Meat and Offal: 10 days Milk: 84 hours (7 milkings) Intravenous Use Meat and Offal: 4 days Milk: 72 hours (6 milkings) Pigs: Intramuscular Use: Meat and Offal: 10 days

Baytril 50mg - 100ml

144650
Dogs and Cats Treatment of bacterial infections of the alimentary, respiratory and urogenital tracts, skin, secondary wound infections and otitis externa where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice. Cattle Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and secondary bacterial infections subsequent to viral conditions (e.g. viral pneumonia) where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice. Pigs Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, actinobacillosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and mulifactorial diseases such as atrophic rhinitis and enzootic pneumonia, where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice. Active ingredient: Enrofloxacin

Baytril Max - 100ml

196410
Cattle For the treatment of respiratory tract infections caused by enrofloxacin-sensitive Histophilus somni, Mannheimia haemolytica, Pasteurella multocida and Mycoplasma spp. For the treatment of Mastitis caused by enrofloxacin-sensitive E. coli. Pigs For the treatment of bacterial bronchopneumonia caused by enrofloxacin-sensitive Actinobacillus pleuropneumoniae, Pasteurella multocida and complicated by Haemophilus parasuis as secondary pathogen in pigs. VPA 10021/065/001. Active ingredient: Enrofloxacin

Betamox L.A. - 100ml

117060
Suitable for the control of infections, due to susceptible micro-organisms, in cattle, sheep, pigs, dogs and cats where a single injection giving prolonged activity is required. It may also protect from secondary bacterial invasion in cases where bacteria are not the initial cause of disease. Indications include infections of: Alimentary tract, Respiratory tract, Skin and soft tissue, Urogenital tract, In prevention of post-operative infection (treat before surgery). Active ingredient: Amoxicillin

Betamox R.T.U. - 100ml

117070
Is a broad spectrum semi-synthetic penicillin, bactericidal in action for use in cattle, sheep, pigs, dogs and cats. In vitro it is effective against a wide range of Gram-positive and Gram-negative pathogenic bacteria. Active ingredient: Amoxicillin

Betamox R.T.U. - 50ml

111601
Is a broad spectrum semi-synthetic penicillin, bactericidal in action for use in cattle, sheep, pigs, dogs and cats. In vitro it is effective against a wide range of Gram-positive and Gram-negative pathogenic bacteria. Active ingredient: Amoxicillin

Borgal 24% - 100ml

100390
Indications Treatment of infections caused by bacteria sensitive to the combination of antibiotics, such as infections of the respiratory, gastro-intestinal and urino-genital tract and infections of the joints or skin. Active ingredient: Trimethoprim, Sulfadoxin.

Cadorex - 100ml

158134
For treatment Cattle: Intramuscular route: 20 mg of florfenicol/kg bodyweight (equivalent to 1 ml of the product/15 kg bodyweight) to be administered twice 48 hours apart using a 16 gauge needle. Subcutaneous route: 40 mg of florfenicol/kg bodyweight (equivalent to 2 ml of the product/15 kg bodyweight) to be administered once using a 16 gauge needle. The dose volume given at any one injection site should not exceed 10 ml. The injection should only be given in the neck. Sheep: 20 mg of florfenicol/kg bodyweight (equivalent to 1 ml of the product/15 kg bodyweight) by intramuscular injection daily for three consecutive days. The volume administered per injection site should not exceed 4 ml. Pharmacokinetic studies showed that mean plasma concentrations remain above MIC90 (1 µg/ml) for up to 18 hours after administration of the product at the recommended treatment dose. The pre-clinical data provided support the recommended treatment interval (24 hours) for target pathogens with MIC up to 1 µg/ml. Pigs: 15 mg of florfenicol/kg bodyweight (equivalent to 1 ml of the product/20 kg bodyweight) by intramuscular injection into the neck muscle twice at 48 hours intervals using a 16-gauge needle. The volume administered per injection site should not exceed 3 ml. For intramuscular, it is recommended to treat animals in the early stages of disease and to evaluate the response to treatment within 48 hours after the second injection. If clinical signs of respiratory disease persist 48 hours after the last injection, treatment should be changed using another formulation or another antibiotic and continued until clinical signs have resolved. Withdrawals Cattle: Meat and offal: by IM route: 30 days by SC route: 44 days Cattle Milk: Not authorised for use in lactating animals producing milk for human consumption including pregnant animals intended to produce milk for human consumption. Sheep: Meat and offal:by IM route: 39 days Sheep Milk:Not authorised for use in lactating animals producing milk for human consumption including pregnant animals intended to produce milk for human consumption. Pigs:Meat and offal: by IM route: 18 days