Banamine Injectable Solution is an anti-inflammatory and analgesic.
Used in horses for the alleviation of inflammation and pain associated with musculoskeletal disorders and for te alleviation of visceral pain associated with colic.
Indicated for the treatment of bovine respiratory disease (BRD) in beef and non-lactating dairy cattle and for treatment and control of swine respiratory disease (SRD) in swine.
Each ml of Baytril 100 injectable solution contains 100 mb enrofloxacin.
Indicated for the treatment of bovine respiratory disease (BRD) in beef and non-lactating dairy cattle and for treatment and control of swine respiratory disease (SRD) in swine.
Each ml of Baytril 100 injectable solution contains 100 mb enrofloxacin.
Indicated for the treatment of bovine respiratory disease (BRD) in beef and non-lactating dairy cattle and for treatment and control of swine respiratory disease (SRD) in swine.
Each ml of Baytril 100 injectable solution contains 100 mb enrofloxacin.
For the treatment of disease in dairy cattle, beef cattle and swine. Ready-to-use solution of the broad-spectrum antibiotic oxytetracycline by injection. Delivers rapid sustainable blood levels.
Indicated for the treatment of the following diseases in dairy cattle and beef cattle when due to oxytetracycline-susceptible organisms: pneumonia, shipping fever complex, pinkeye, footrot, diphtheria, lepto, wound infections and acute metritis.
Bo-Se is recommended for the prevention and treatment of white muscle disease syndrome in calves, lambs, and ewes, and as an aid in the prevention and treatment of Selenium-Tocopherol Deficiency in sows and weanling pigs.
CEFENIL RTU is indicated for treatment/control of swine bacterial respiratory disease (swine bacterial pneumonia) associated with Actinobacillus (Haemophilus) pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis and Streptococcus suis. Cattle: CEFENIL RTU is indicated for treatment of the following bacterial diseases: Bovine respiratory disease (BRD, shipping fever, pneumonia) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni. Acute bovine interdigital necrobacillosis (foot rot, pododermatitis) associated with Fusobacterium necrophorum and Bacteroides melaninogenicus. Acute metritis (0 to 14 days post-partum) associated with bacterial organisms susceptible to ceftiofur. Do not store above 30 deg C (86 deg. F). Protect from freezing. FDA Approved, Zero Milk Discard, Ready-To-Use Formulation, Multi day Treatment Regimen.
CEFENIL RTU is indicated for treatment/control of swine bacterial respiratory disease (swine bacterial pneumonia) associated with Actinobacillus (Haemophilus) pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis and Streptococcus suis. Cattle: CEFENIL RTU is indicated for treatment of the following bacterial diseases: Bovine respiratory disease (BRD, shipping fever, pneumonia) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni. Acute bovine interdigital necrobacillosis (foot rot, pododermatitis) associated with Fusobacterium necrophorum and Bacteroides melaninogenicus. Acute metritis (0 to 14 days post-partum) associated with bacterial organisms susceptible to ceftiofur. Do not store above 30 deg C (86 deg. F). Protect from freezing. FDA Approved, Zero Milk Discard, Ready-To-Use Formulation, Multiday Treatment Regimen.
For use as an aid in the treatment of hypocalcemia (parturient paresis, milk fever), hypomagnesemia (grass tetany), and other conditions associated with calcium, magnesium, phosphorus, and potassium deficiencies in cattle.
A single, subcutaneous injection of 1.14 mL/100 lb. (2.5 mg/kg) of bodyweight delivers a full course of therapy, thereby minimizing labor and handling stress.
DRAXXIN Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass; triamilide. Each mL of DRAXXIN contains 100 mg of tulathromycin as the free base in a 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), with citric and hydrochloric acids added to adjust pH.
A single, subcutaneous injection of 1.14 mL/100 lb. (2.5 mg/kg) of bodyweight delivers a full course of therapy, thereby minimizing labor and handling stress.
DRAXXIN Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass; triamilide. Each mL of DRAXXIN contains 100 mg of tulathromycin as the free base in a 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), with citric and hydrochloric acids added to adjust pH.
A single, subcutaneous injection of 1.14 mL/100 lb. (2.5 mg/kg) of bodyweight delivers a full course of therapy, thereby minimizing labor and handling stress.
DRAXXIN Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass; triamilide. Each mL of DRAXXIN contains 100 mg of tulathromycin as the free base in a 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), with citric and hydrochloric acids added to adjust pH.
A single, subcutaneous injection of 1.14 mL/100 lb. (2.5 mg/kg) of bodyweight delivers a full course of therapy, thereby minimizing labor and handling stress.
DRAXXIN Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass; triamilide. Each mL of DRAXXIN contains 100 mg of tulathromycin as the free base in a 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), with citric and hydrochloric acids added to adjust pH.
An FDA-approved sterile, ready-to-use injectable antimicrobial solution that contains enrofloxacin, a broad-spectrum fluoroquinolone antimicrobial agent.
Approved for Single Dose & Multi-Day Treatment and Control
An FDA-approved sterile, ready-to-use injectable antimicrobial solution that contains enrofloxacin, a broad-spectrum fluoroquinolone antimicrobial agent.
Approved for Single Dose & Multi-Day Treatment and Control
An FDA-approved sterile, ready-to-use injectable antimicrobial solution that contains enrofloxacin, a broad-spectrum fluoroquinolone antimicrobial agent.
Approved for Single Dose & Multi-Day Treatment and Control
The luteolytic action of Estrumate can be utilized to manipulate the estrous cycle to better fit certain management practices, terminal pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function
The luteolytic action of Estrumate can be utilized to manipulate the estrous cycle to better fit certain management practices, terminal pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function
Flunixin is a synthetic drug more commonly made into flunixin meglamine, which is the primary component of Banamine, commonly used for pain, inflammation and pyrexia associated with colic, musculoskeletal disorders and various respiratory conditions in horses.
Increxxa contains tulathromycin, the same macrolide antibiotic veterinarians and the cattle industry have depended on to control and treat bovine respiratory disease (BRD) in cattle for more than 15 years. It's a go-to antibiotic for beef and dairy producers because of its one-time use, extended duration of action, ease of administration and broad-spectrum control
Increxxa contains tulathromycin, the same macrolide antibiotic veterinarians and the cattle industry have depended on to control and treat bovine respiratory disease (BRD) in cattle for more than 15 years. It's a go-to antibiotic for beef and dairy producers because of its one-time use, extended duration of action, ease of administration and broad-spectrum control
For use in chickens up to 7 days of age as an aid in the control of airsacculitis caused by either Mycoplasma Synoviae or Mycoplasma gallisepticum susceptible to lincomycin-spectinomycin.
Complicated Chronic Respiratory disease (Air Sac Infection) caused by Escherichia Coli and M. Gallisepticum susceptible to lincomycin-spectinomycin.
LongRange contains eprinomectin , an extended release injectable parasiticide for cattle on pastures useful for the treatment and control of roundworms, lungworms, grubs, and mites.
Each ml of LongRange contains 50 mg eprinomectin, a macrocyclic lactone.
LongRange contains eprinomectin , an extended release injectable parasiticide for cattle on pastures useful for the treatment and control of roundworms, lungworms, grubs, and mites.
Each ml of LongRange contains 50 mg eprinomectin, a macrocyclic lactone.
LongRange contains eprinomectin , an extended release injectable parasiticide for cattle on pastures useful for the treatment and control of roundworms, lungworms, grubs, and mites.
Each ml of LongRange contains 50 mg eprinomectin, a macrocyclic lactone.
In beef and non-lactating dairy cattle, Macrosyn is approved for the control & treatment of bovine respiratory disease (BRD) (Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Mycoplasma bovis), treatment of bovine foot rot (Fusobacterium necrophorum, Porphyromonas levii), and treatment of pink eye (Moraxella bovis)
In calves (suckling, dairy and veal calves) Macrosyn is approved for the treatment of bovine respiratory disease (BRD) (M. haemolytica, P. multocida, H. somni, M. bovis)
In beef and non-lactating dairy cattle, Macrosyn is approved for the control & treatment of bovine respiratory disease (BRD) (Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Mycoplasma bovis), treatment of bovine foot rot (Fusobacterium necrophorum, Porphyromonas levii), and treatment of pink eye (Moraxella bovis)
In calves (suckling, dairy and veal calves) Macrosyn is approved for the treatment of bovine respiratory disease (BRD) (M. haemolytica, P. multocida, H. somni, M. bovis)
In beef and non-lactating dairy cattle, Macrosyn is approved for the control & treatment of bovine respiratory disease (BRD) (Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Mycoplasma bovis), treatment of bovine foot rot (Fusobacterium necrophorum, Porphyromonas levii), and treatment of pink eye (Moraxella bovis)
In calves (suckling, dairy and veal calves) Macrosyn is approved for the treatment of bovine respiratory disease (BRD) (M. haemolytica, P. multocida, H. somni, M. bovis)
Micotil is indicated for the control of respiratory disease in cattle at high risk of developing BRD associated with Mannheimia haemolytica.
For the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni and for the treatment of bovine respiratory disease (ORD) associated with Mannheimia haemolytica.
The recommended dosage is 1 ml per 100 lbs body weight for calves up to 1 year of age; 1 ml per 150 lbs for cattle 1-2 years of age; and 1 ml per 200 lbs for cattle over 2 years of age.
Multimin 90 should be administered to cattle by SQ or IM injection.
An antihistamine injectable solution for cattle and horses. This rapid acting antihistamine contains the active ingredient, tripelennamine hydrochloride to block harmful histamine effects which can delay recovery time. Labeled for beef and dairy cattle calves (2 months of age and older) and horses.
Do not administer more than 10 ml per injection site.
Resflor Gold is an antibiotic and anti-inflammatory 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.
Do not administer more than 10 ml per injection site.
Resflor Gold is an antibiotic and anti-inflammatory 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.
Do not administer more than 10 ml per injection site.
Resflor Gold is an antibiotic and anti-inflammatory 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.
Indicated for the treatment of bovine respiratory disease (pneumonia) associated with Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni in beef and dairy cattle.
Do not use in calves to be processed for veal. Do not use in female dairy cattle 20 months of age or older.
SPECTRAMAST DC is indicated for the treatment of subclinical mastitis in dairy cattle at the time of dry off associated with Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis.
Infuse one (1) syringe into each affected quarter at the time of dry off.
Spectramast LC is indicated for the treatment of clinical mastitis in lactating dairy cattle associated with coagulase-negative staphylococci, Streptococcus dysgalactiae, and Escherichia coli.
Dosage: Each 10 ml tube of Spectramast LC contains the equivalent to 125 mg ceftiofur in a cottonseed oil base. Infuse one tube into each affected quarter.
Treat as well as help prevent secondary infections and scours. For oral administration in beef and dairy calves for the control and treatment of bacterial enteritis caused by Salmonella typhimurium and E. coli, and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida. Yellow color.
Treat as well as help prevent secondary infections and scours. For oral administration in beef and dairy calves for the control and treatment of bacterial enteritis caused by Salmonella typhimurium and E. coli, and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida. Yellow color.
One-day antibiotic mastitis treatment for lactating dairy cows in ready-to-use, disposable syringes. For effective intramammary infusion into the lactating cow. Provides bactericidal activity against both gram-positive and gram-negative bacteria, especially penicillin-resistant Streptococcus agalactiae and Staphylococcus aureus.
Valcor is indicated for the treatment and control of internal and external parasites in beef cattle 2 months of age or older and in replacement dairy heifers less than 20 months of age. Not for use in beef bulls intended for breeding over 1 year of age, dairy calves, and veal calves.
Valcor is indicated for the treatment and control of internal and external parasites in beef cattle 2 months of age or older and in replacement dairy heifers less than 20 months of age. Not for use in beef bulls intended for breeding over 1 year of age, dairy calves, and veal calves.
Valcor is indicated for the treatment and control of internal and external parasites in beef cattle 2 months of age or older and in replacement dairy heifers less than 20 months of age. Not for use in beef bulls intended for breeding over 1 year of age, dairy calves, and veal calves.
Vitamin K1 Injection is indicated in coagulation disorders when caused by vitamin K deficiency or interference with vitamin K activity; to counter hypoprothrombinemia induced by ingestion of anticoagulant rodenticides; or to counter hypoprothrombinemia caused by consumption of bishydroxycoumarin found in spoiled and moldy sweet clover
Vitamin K1 Injection contains 10 mg phytonadione per ml. The dosage range for cattle, calves, horses, swine, sheep and goats is 0.5 - 2.5 mg/kg SQ or IM. The dosage range for dogs and cats is 0.25 - 5mg/kg SQ or IM
Zuprevo 180 mg/ml is licensed for the treatment and prevention of bovine respiratory disease (BRD) associated with M. haemolytica, P. multocida and H.somni sensitive to tildipirosin.
Zuprevo contains the active tildipirosin - a 16-membered tribasic macrolide antibiotic unique to MSD Animal Health.
Zuprevo 180 mg/ml is licensed for the treatment and prevention of bovine respiratory disease (BRD) associated with M. haemolytica, P. multocida and H.somni sensitive to tildipirosin.
Zuprevo contains the active tildipirosin - a 16-membered tribasic macrolide antibiotic unique to MSD Animal Health.