Livestock Prescriptions Online

Prescription items are NON-RETURNABLE and NON-REFUNDABLE *** CURRENT EXPIRATION DATE FOR 500ML BAG 06/30/2024 *** *** CURRENT EXPIRATION DATE FOR 1000ML BAG 08/31/2025 *** Common Brand Names - Manufacturer varies. Product label and bag design may be different than shown. Storage - Store in manufacturer's packaging at room temperature. Uses - Used to maintain hydration or to rehydrate animals in many situations including the treatment of shock, decreased oral fluid intake, and to replace fluids lost due to an illness such as kidney disease. Dose and Administration - The dose is dependent upon the age, weight and clinical condition of the patient. As reported in the literature, the dosage and constant infusion rate of intravenous dextrose must be selected with caution in pediatric patients, particularly neonates and low birth weight infants, because of the increased risk of hyperglycemia/hypoglycemia. Possible Side Effects - Side effects are unlikely if the proper dose is given. Abscesses or infection may occur at the injection site if a sterile needle and proper technique were not used during administration. If your pet experiences an allergic reaction to the medication, signs may include facial swelling, hives, scratching, sudden onset of diarrhea, vomiting, shock, seizures, pale gums, cold limbs, or coma. If you observe any of these signs, contact your veterinarian immediately. Precautions - Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store. The presence of calcium limits their compatibility with certain drugs that form precipitates of calcium salts and also prohibits their simultaneous infusion through the same administration set as blood because of the likelihood of coagulation. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Drug, Food, and Test Interactions - Consult your veterinarian before using lactated ringer injection with any other medications, including vitamins and supplements, since interactions may occur. Some injectable medications are not compatible with the components in LRS. Consult with your veterinarian before adding any medications to the bag of LRS. No known food interactions. Signs of Toxicity/Overdose - If an animal becomes overhydrated (too much fluid is given), blood potassium levels may become too low, causing muscle and heart abnormalities. Signs may include weakness, constipation, rapid breathing, and increased heart rate. Overhydration may also cause fluid to accumulate in the lungs (pulmonary edema) and increase the workload for the heart. Signs may include increased or rapid breathing, coughing, or wheezing. If you notice any of these signs, stop fluid therapy and contact your veterinarian immediately. ** This information may not cover all possible uses, directions, side effects, precautions, allergic reactions, drug interactions, or withdrawal times. Always consult your own veterinarian for specific advice concerning the treatment of your pet. « Read less

Prescription items are NON-RETURNABLE and NON-REFUNDABLE *** CURRENT EXPIRATION DATE FOR 500ML BAG 06/30/2024 *** *** CURRENT EXPIRATION DATE FOR 1000ML BAG 08/31/2025 *** Common Brand Names - Manufacturer varies. Product label and bag design may be ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Sulfadimethoxine 12.5% Oral Solution Gallon A broad-spectrum antibacterial oral solution to be supplied in drinking water that will control a variety of diseases such as coccidiosis, fowl cholera, and bacterial pneumonia. Designed to treat and protect chickens, turkeys, dairy calves, dairy heifers and beef cattle from these unhealthy diseases. Broiler and Replacement Chickens: Use for the treatment of disease outbreaks of coccidiosis, fowl cholera, and infectious coryza. Meat Producing Turkeys: Use for the treatment of disease outbreaks of coccidiosis and fowl cholera. Dairy Calves, Dairy Heifers and Beef Cattle: Use for the treatment of shipping fever complex, and bacterial pneumonia associated with Pasteurella spp. sensitive to sulfadimethoxine; and calf diphtheria and foot rot associated with Fusobacterium necrophorum sensitive to sulfadimethoxine. Directions TREATMENT PERIOD - 6 consecutive days Species Concentration Use Directions CHICKENS 0.05% Add 1 fl oz* to 2 gallons of drinking water or 25 fl oz to 50 gallons of drinking water TURKEYS 0.025% Add 1 fl oz* to 4 gallons of drinking water or 25 fl oz to 100 gallons of drinking water Automatic Proportioners** Stock Solution - To make 2 gallons of Stock Solution use: CHICKENS Add 1 gal Sulfadimethoxine 12.5% Oral Solution to 1 gal of water TURKEYS Add 2 qts Sulfadimethoxine 12.5% Oral Solution to 6 qts of water * 1 fl oz Sulfadimethoxine 12.5% Oral Solution = 30 mL or 2 tablespoonfuls ** Set proportioner to a feed rate of 1 fl oz of Sulfadimethoxine Stock Solution per gallon of water. TREATMENT PERIOD - 5 consecutive days DAIRY CALVES, DAIRY HEIFERS AND BEEF CATTLE Dosage: SULFADIMETHOXINE IN WATER 25 mg/lb first day followed by 12.5 mg/lb/day for 4 days. WATER CONSUMPTION (SUMMER) (WINTER) 1 gallon/† 100 lb b.w. 1 gallon/† 150 lb b.w. FIRST DAY ADD: 1 pint (16 fl oz) to: 25 gallons 16 gallons 1 quart (32 fl oz) to: 50 gallons 33 gallons 1 gallon (128 fl oz) to: 200 gallons 127 gallons NEXT 4 DAYS ADD: 1 pint (16 fl oz) to: 50 gallons 33 gallons 1 quart (16 fl oz) to: 100 gallons 66 gallons 1 gallon (128 fl oz) to: 400 gallons 266 gallons †Dosage recommendations are based on an estimated summer water intake of 1 gal of water for every 100 lb of body weight per day, and an estimated winter water intake of 1 gal of water for every 150 lb of body weight per day. For individual treatment of cattle, Sulfadimethoxine 12.5% Oral Solution may be given as a drench. Administer using an initial dose of 25 mg/lb followed by 4 maintenance doses of 12.5 mg/lb/day. One fl oz will medicate one 150 lb animal initially and 1/2 fl oz will medicate one 150 lb animal on a maintenance dose. Cautions Store at room temperature; if freezing occurs, thaw and shake well prior to use. Protect from light; direct sunlight may cause discoloration. Freezing or discoloration does not affect potency. Prepare a fresh stock solution daily. Chickens and Turkeys: If animals show no improvement within 5 days, discontinue treatment and re-evaluate diagnosis. Handle the recommended dilutions (chickens 0.05% and turkeys 0.025%) as regular drinking water. Administer as a sole source of drinking water and sulfonamide medication. Chickens and turkeys that have survived fowl cholera outbreaks should not be kept for replacement or breeders. Cattle: During the treatment period, make certain that animals maintain adequate water intake. If animals show no improvement within 2 or 3 days, re-evaluate diagnosis. Treatment should not be continued beyond 5 days. Residue Warnings Chickens and Turkeys: Withdraw 5 days before slaughter. Do not administer to chickens over 16 weeks (112 days) of age or to turkeys over 24 weeks (168 days) of age. Cattle: Withdraw 7 days before slaughter. For dairy calves, dairy heifers and beef cattle only. A withdrawal period has not been established for this product in pre-ruminating calves. DO NOT USE IN CALVES TO BE PROCESSED FOR VEAL. Store at controlled room temperature 22°-25°C (68°-77°F). Shake well before use. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Sulfadimethoxine 12.5% Oral Solution Gallon A broad-spectrum antibacterial oral solution to be supplied in drinking water that will control a variety of diseases such as coccidiosis, fowl chole ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Banamine Injection How Supplied BANAMINE Solution Injectable, 50 mg flunixin/mL (equivalent to 83 mg flunixin meglumine/mL) is available in 50, 100 and 250 mL multidose vials. Description Each milliliter of BANAMINE Solution Injectable contains: Active ingredient: 50 mg flunixin equivalent to 83 mg flunixin meglumine USP; Non-medicinal Ingredients: 0.1 mg edetate disodium, 2.5 mg sodium formaldehyde sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol; 5.0 mg phenol as preservative, hydrochloric acid, water for injection q.s. Banamine Solution Injectable Indications Horses BANAMINE Solution Injectable is recommended for the alleviation of inflammation and associated pain in musculoskeletal disorders in the horse. BANAMINE Solution Injectable is also recommended for the alleviation of visceral pain associated with colic in the horse. Cattle BANAMINE Solution Injectable is indicated for the control of pyrexia associated with Bovine Respiratory Disease (BRD), endotoxemia and acute bovine mastitis. BANAMINE Solution Injectable is also indicated for the control of inflammation associated with endotoxemia. BANAMINE Solution Injectable used as an adjunct to antibiotic therapy with oxytetracycline has been demonstrated to control pyrexia associated with bovine respiratory disease. Action Flunixin meglumine is a potent, non-narcotic, non-steroidal, analgesic agent with anti-inflammatory activity. Antipyretic activity has been demonstrated in cattle and in laboratory animals. It is significantly more potent than pentazocine, meperidine and codeine as an analgesic in the rat yeast paw test. Horse Flunixin is four times as potent on a mg per mg basis as phenylbutazone as measured by the reduction in lameness and swelling in the horse. Plasma half-life in horse serum is 1.6 hours following a single dose of 1.1 mg/kg. Measurable amounts are detectable in horse plasma at 8 hours post injection. Cattle Flunixin meglumine is a weak acid (pKa = 5.82) which exhibits a high degree of plasma protein binding (app. 99%). However, free (unbound) drug appears to readily partition into body tissues (Vss predictions range from 297 to 782 mL/kg). Total body water is approximately 570 mL/kg. In cattle, elimination occurs primarily through biliary excretion. This may, at least in part, explain the presence of multiple peaks in the blood concentration/time profile following IV administration. In healthy cattle, total body clearance has been reported to range from 90 to 150 mL/kg/hr. These studies also report a large discrepancy between the volume of distribution at steady state (Vss) and the volume of distribution associated with the terminal elimination phase (Vβ). This discrepancy appears to be attributable to extended drug elimination from a deep compartment. The terminal half-life has been shown to vary from 3.14 to 8.12 hours. Model and field studies have shown that flunixin can have short-term effect in the control of some inflammatory factors associated with endotoxemia and irritation (carregeenan). Flunixin persists in inflammatory tissues and is associated with anti-inflammatory properties which extend well beyond the period associated with detectable plasma drug concentrations. These observations account for the counterclockwise hysteresis associated with flunixin's pharmacokinetic/pharmacodynamic relationship. Therefore, prediction of drug concentrations based upon the estimated plasma terminal half-life will likely underestimate both the duration of drug action and the concentration of drug remaining at the site of activity. Banamine Solution Injectable Dosage And Administration Horses The recommended dose for musculoskeletal disorders is 1.1 mg per kg (1 mL/45 kg) of body weight once daily. Treatment may be given by intravenous or intramuscular injection and repeated for up to 5 days. Intravenous studies show that the onset of activity is within 2 hours. Peak response occurs between 12 and 16 hours and duration of activity is 24 to 36 hours following intravenous and intramuscular administration. The recommended dose for the alleviation of pain associated with equine colic is 1.1 mg per kg of body weight. Intravenous administration is recommended for prompt relief. Should colic symptoms recur, treatment may be repeated as necessary. Clinical studies show that pain symptoms were alleviated in 37% of treated horses within 15 minutes, and 74% within 30 minutes. The cause of colic should be determined and treated with concomitant therapy. Cattle The recommended dose for control of pyrexia associated with bovine respiratory disease and endotoxemia and control of inflammation associated with endotoxemia in cattle is 2.2 mg flunixin per kg (2 mL/45 kg) of body weight given by slow intravenous administration once a day for up to 3 days. The total daily dose should not exceed 2.2 mg/kg of body weight. Avoid rapid intravenous administration of the drug. Twenty-four (24) hours after administration, check if animal is febrile. Re-administer only if the fever is 104°F (40°C) or higher. The recommended dose for control of pyrexia associated with acute bovine mastitis is 2.2 mg flunixin per kg of body weight given as a single intravenous injection. Administer slowly. Contraindications Horse Do not administer intra-arterially. Inadvertent intra-arterial injection may cause adverse reactions. Signs can be ataxia, incoordination, hyperventilation, hysteria, and muscle weakness. Signs are transient and disappear without antidotal medication within a few minutes. Do not use in horses showing hypersensitivity to flunixin meglumine. Cattle Do not administer intra-arterially. Inadvertent intra-arterial injection may cause adverse reactions. Do not use in cattle showing hypersensitivity to flunixin meglumine. The drug is contraindicated in animals with hepatic disease, renal and cardiovascular impairment, gastro-intestinal ulceration and/or platelet disorders. It is also contra-indicated in dehydrated animals. Precautions The use of NSAIDS may be associated with gastro-intestinal and renal toxicity. Patients at greatest risk for renal toxicity are those that are dehydrated, on concomitant diuretic therapy or those with renal, cardiovascular, and/or hepatic dysfunction. Due to the potential for NSAIDs to induce gastro-intestinal ulceration, concomitant use of this drug with other anti-inflammatory drugs, such as other NSAIDs and corticosteroids should be avoided. With the exception of the antibiotic oxytetracycline in cattle, studies to determine the activity of BANAMINE when administered concomitantly with other drugs have not been conducted. Drug compatibility should be monitored closely. Discontinue use if hematuria or fecal blood are observed. Avoid rapid intravenous administration of the drug. Horses The effect of BANAMINE on reproduction in horses has not been determined. Studies on reproduction in rats and rabbits have shown no teratogenicity. Cattle Do not use in bulls intended for breeding as reproductive effects of BANAMINE in this class of cattle have not been investigated. NSAIDs are known to have potential effects on both parturition and the estrous cycle. There may be a delay in the onset of estrus if flunixin is administered during the prostaglandin phase of the estrous cycle. The effects of flunixin on imminent parturition have not been evaluated in a controlled study. NSAIDs are known to have the potential to delay parturition through a tocolytic effect. Do not exceed the recommended dose. Side Effects During clinical studies no significant side effects were reported when the drug was injected slowly. In cattle, a temporary head thrashing can occur if the drug is injected too rapidly. Toxicity No toxic effects were observed in rats given intramuscular flunixin 4 mg/kg/day for 28 days. No adverse effects were seen in dogs given a single intramuscular injection of 50 mg/kg. Higher doses resulted in salivation, p « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Banamine Injection How Supplied BANAMINE Solution Injectable, 50 mg flunixin/mL (equivalent to 83 mg flunixin meglumine/mL) is available in 50, 100 and 250 mL multidose vials. Description Each ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Neomycin Oral Solution 16oz Neomycin is indicated for the treatment and control of bacterial enteritis (scours) caused by E.coli susceptible to Neomycin Sulfate in cattle (except veal calves), swine sheep and goats. Neomycin Oral Solution Caution To administer the stated dosage, the concentration of neomycin required in medicated water must be adjusted to compensate for variation in age and weight of animal, the nature and severity of disease signs, and environmental temperature and humidity, each of which affects water consumption. Contains Per Ml: Neomycin Sulfate 200 Mg Equivalent To 140 Mg Neomycin If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. If symptoms such as fever, depression, or going off feed develop, oral neomycin is not indicated as the sole treatment since systemic levels of neomycin are not obtained due to low absorption from the gastrointestinal tract. Important Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Animals not drinking or eating should be treated individually by drench. Residue Warnings Not for human use. Keep out of reach of children. Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species: Cattle - 1 day, Sheep - 2 days, Swine and Goats - 3 days. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Use Of More Than One Product Containing Neomycin Or Failure To Follow Withdrawal Times May Result In Illegal Drug Residues. Store at controlled room temperature 20° to 25°C (68° to 77° F) (see USP). * Teaspoon (tsp) / Tablespoon (tbsp) is equal to U.S. Standard Measure. Neomycin Oral Solution Dosage And Administration Administer to cattle, swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight in divided doses for a maximum of 14 days. Dosage Schedule For Treatment Of Colibacillosis Pounds of Body Weight/Amount of Neomycin Oral Solution Per Day in Divided Doses 25 lb - 1.2 mL (1/4 tsp*) 50 lb - 2.5 mL (1/2 tsp*) 100 lb - 5 mL (1 tsp*) 300 lb - 15 mL (1 tbsp*) 591.5 lb - 29.5 mL (1 fl oz) Neomycin Solution may be given undiluted or diluted with water. Herd Treatment: Each 473 mL (16 Fl Oz) bottle will treat 9,600 pounds body weight. Each 3.785 L (1 Gal) bottle will treat 76,800 pounds body weight. Therefore, estimate the total number of pounds body weight of the animals to be treated and administer one (1) fluid ounce for each 600 pounds. The product should be added to the amount of drinking water to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) teaspoon in water or milk for each 100 pounds body weight. Administer daily either as a drench in divided dosages or in the drinking water to be consumed in 12-24 hours. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Neomycin Oral Solution 16oz Neomycin is indicated for the treatment and control of bacterial enteritis (scours) caused by E.coli susceptible to Neomycin Sulfate in cattle (except veal calves), ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Cystorelin Injection expiration date 5/2021. CYSTORELIN (R) is indicated for the treatment of ovarian follicular cysts in dairy cattle. Ovarian cysts are non-ovulated follicles with incomplete luteinization which result in nymphomania or irregular estrus. Historically, cystic ovaries have responded to an exogenous source of luteinizing hormone (LH) such as human chorionic gonadotropin. CYSTORELIN (R) initiates release of endogenous LH to cause ovulation and luteinization. The recommended intravenous or intramuscular dosage of CYSTORELIN (R) is 100 mcg (2 mL) per cow. Ingredients: Each mL of CYSTORELIN (R) contains: Gonadorelin diacetate tetrahydrate 50 mcg Benzyl Alcohol 9 mg Sodium Chloride 7.47 mg Water for Injection, U.S.P. q.s. pH adjusted with potassium phosphate (monobasic and dibasic). Storage: Keep at or below 77°f, a brief excursion to 86°f permitted. Discard Remaining Product 90 Days After First Use. Endogenous gonadorelin is synthesized and/or released from the hypothalamus during various stages of the bovine estrus cycle following appropriate neurogenic stimuli. It passes via the hypophyseal portal vessels, to the anterior pituitary to effect the release of gonadotropins (e.g. LH, FSH). Synthetic gonadorelin administered intravenously or intramuscularly also causes the release of endogenous LH or FSH from the anterior pituitary. Gonadorelin diacetate tetrahydrate has been shown to be safe. The LD50 for mice and rats is greater than 60 mg/kg, and for dogs, greater than 600 mcg/kg, respectively. No untoward effects were noted among rats or dogs administered 120 mcg/kg/day or 72 mcg/kg/day intravenously for 15 days. It has no adverse effects on heart rate, blood pressure, or EKG to unanesthetized dogs at 60 mcg/kg. In anesthetized dogs, it did not produce depression of myocardial or system hemodynamics or adversely affect coronary oxygen supply or myocardial oxygen requirements. The intravenous administration of 60 mcg/kg/day of gonadorelin diacetate tetrahydrate to pregnant rats and rabbits during organogenesis did not cause embryotoxic or teratogenic effects. The intramuscular administration of 1000 mcg to normally cycling dairy cattle had no effect on hematology or blood chemistry. Further, CYSTORELIN (R) does not cause irritation at the site of intramuscular administration in dogs. The dosage administered was 72 mcg/kg/day for seven (7) days. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Cystorelin Injection expiration date 5/2021. CYSTORELIN (R) is indicated for the treatment of ovarian follicular cysts in dairy cattle. Ovarian cysts are non-ovulated follicles with incomplete ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Multi Min 90 Injection 500ml Multimin 90 is a supplemental source of zinc, manganese, selenium and copper for cattle. Each ml of Multimin 90 is a chelated source of 60 mg zinc, 10 mg manganese, 5 mg selenium and 15 mg copper. Multimin 90 should be administered to cattle by SQ or IM injection. DIRECTIONS: This product is only for use in cattle. MULTIMIN(R)90 is to be given subcutaneously (under the skin) ONLY. It is recommended to administer the product in accordance with Beef Quality Assurance (BQA) guidelines. Minimum distance between injection sites for MULTIMIN(R)90 product and other injection sites should be at least 4 inches. Inject under the loose skin of the middle of the side of the neck. Max volume per injection site is 7ml. Subcutaneous injection in the middle side of the neck. CAUTION : Slight local reaction may occur for about 30 seconds after injection. A slight swelling may be observed at injection site for a few days after administration. Use standard aseptic procedures during administration of injections to reduce the risk of injection site abscesses or lesions. PRECAUTIONS: Selenium and copper are toxic if administered in excess. Always follow recommended label dose. Do not overdose. If it recommended that accurate body weight is determined prior to treatment. Do not use concurrently with other injectable selenium and copper products. Do not use concurrently with selenium or copper boluses. Do not use in emaciated cattle with a BCS of 1 in dairy or 1-3 in beef. Consult your veterinarian. STORAGE: Store between 15° C and 30° C (59° F and 86° F) « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Multi Min 90 Injection 500ml Multimin 90 is a supplemental source of zinc, manganese, selenium and copper for cattle. Each ml of Multimin 90 is a chelated source of 60 mg zinc, 10 mg manganese, ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Cattle - Single-Dose Therapy: Baytril (R) 100 (enrofloxacin) Injectable is indicated for the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis in beef and non-lactating dairy cattle; and for the control of BRD in beef and non-lactating dairy cattle at high risk of developing BRD associated with M. haemolytica, P. multocida, H. somni and M. bovis . Cattle - Multiple-Day Therapy: Baytril 100 is indicated for the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni in beef and non-lactating dairy cattle. Swine: Baytril 100 is indicated for the treatment and control of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Haemophilus parasuis, Streptococcus suis, Bordetella bronchiseptica and Mycoplasma hyopneumoniae. Baytril 100 is indicated for the control of colibacillosis in groups or pens of weaned pigs where colibacillosis associated with Escherichia coli has been diagnosed. Storage and Disposal Protect from direct sunlight. Do not refrigerate or freeze. Store at 20-30ºC (68-86ºF), excursions permitted up to 40ºC (104ºF). Precipitation may occur due to cold temperature. To redissolve, warm and then shake the vial. Dosage Information Baytril 100 provides flexible dosages and durations of therapy. Baytril 100 may be administered as a single dose for one day for treatment and control of BRD (cattle), for treatment and control of SRD or for control of colibacillosis (swine), or for multiple days for BRD treatment (cattle). Selection of the appropriate dose and duration of therapy for BRD treatment in cattle should be based on an assessment of the severity of the disease, pathogen susceptibility and clinical response. Cattle: Single-Dose Therapy (BRD Treatment): Administer, by subcutaneous injection, a single dose of 7.5-12.5 mg/kg of body weight (3.4-5.7 mL/100 lb). Multiple-Day Therapy (BRD Treatment): Administer daily, a subcutaneous dose of 2.5-5 mg/kg of body weight (1.1-2.3 mL/100 lb). Treatment should be repeated at 24-hour intervals for three days. Additional treatments may be given on Days 4 and 5 to animals that have shown clinical improvement but not total recovery. Single-Dose Therapy (BRD Control): Administer, by subcutaneous injection, a single dose of 7.5 mg/kg of body weight (3.4 mL/100 lb). « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Cattle - Single-Dose Therapy: Baytril (R) 100 (enrofloxacin) Injectable is indicated for the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella mu ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Epinephrine 1:1000 Injection 50 ml INDICATIONS: For emergency use only in treating anaphylactic shock. Symptoms of anaphylactoid shock include glassy eyes, increased salivation, grinding of teeth, rapid breathing, muscular tremors, staggering gait, and collapse with death following. These symptoms may appear shortly after injection of a bacterin, vaccine or antibiotic. USUAL DOSAGE: Cattle, Horses, Sheep and Swine - 1 cubic centimeter per 100 pounds of body weight. Inject subcutaneously. Store at temperatures between 2°15°C (36°-59°F). KEEP OUT OF REACH OF CHILDREN FOR ANIMAL USE ONLY « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Epinephrine 1:1000 Injection 50 ml INDICATIONS: For emergency use only in treating anaphylactic shock. Symptoms of anaphylactoid shock include glassy eyes, increased salivation, grinding of tee ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE LinxMed SP 40 gram For the treatment of dysentery in swine and for the control of necrotic enteritis in broiler chickens. For oral use in swine and broiler chickens only. Not for use in layer and breeder chickens. Package Size: 40 gram Ingredients: This packet (40 g) contains as active ingredient: Lincomycin hydrochloride Equivalent to lincomycin 16.0 g Dosage: Administer at a dose rate of 64 mg of lincomycin per gallon of drinking water. Treatment Period: Start medication as soon as the diagnosis of necrotic enteritis is determined. The drug should be administered for 7 consecutive days. Administration: This packet (40 g) or one scoop (provided) of this powder will medicate 250 gallons of drinking water providing 64 mg/gallon. This packet (80 g) will medicate 500 gallons of drinking water providing 64 mg/gallon. This packet (160 g) will medicate 1,000 gallons of drinking water providing 64 mg/gallon. This packet (480 g) will medicate 3,000 gallons of drinking water providing 64 mg/gallon. Note: After water medication is discontinued, a recommended control program for necrotic enteritis consists of feeding lincomycin premix at 2 grams lincomycin per ton of complete feed. Precautions: 1. Discard medicated drinking water if not used within 2 days. Fresh stock solution should be prepared daily. 2. If clinical signs of bloody scours (watery, mucoid or bloody stools) have not improved during the first 6 days of medication, discontinue treatment and redetermine the diagnosis. 3. Occasionally, swine fed lincomycin may within the first two days after the onset of treatment develop diarrhea and/or swelling of the anus. On rare occasions, some pigs may show reddening of the skin and irritable behavior. These conditions have been self-correcting within five to eight days without discontinuing the lincomycin treatment. 4. The safety of lincomycin has not been demonstrated for pregnant swine or swine intended for breeding. 5. Do not allow rabbits, hamsters, guinea pigs, horses or ruminants access to water containing lincomycin treatment. Ingestion by these species may result in severe gastrointestinal effects. 6. Do not use the water treatment and the feed treatments simultaneously. 7. Not for use in layer and breeder chickens. Storage: Store at controlled room temperature 20°C to 25°C (68°F to 77°F). « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE LinxMed SP 40 gram For the treatment of dysentery in swine and for the control of necrotic enteritis in broiler chickens. For oral use in swine and broiler chickens only. Not for use in layer a ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Neomix 325 Soluable Powder 100gm For oral use in cattle, swine, sheep, goats and turkeys. For the treatment and control of colibaciliosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves), swine, sheep and goats. For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys. Ingredients Each packet contains: 71.4 g neomycin sulfate (commercial grade) equivalent to 50 g neomycin. Caution Not for use in humans. Keep out of reach of children. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Neomix 325 Soluable Powder 100gm For oral use in cattle, swine, sheep, goats and turkeys. For the treatment and control of colibaciliosis (bacterial enteritis) caused by Escherichia coli suscep ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE LS50 75 gram LS-50 Water Soluble Powder is for use in chickens up to 7 days old to help control chronic respiratory disease (CRD). Lincomycin Spectinomycin Water Soluble Powder contains 16.7 gm of lincoymcin and 33.3 gm of spectinomycin. 1 bottle treats 25 gal of drinking water. This product is indicated 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. Caution: Discard medicated drinking water daily and replace with fresh medicated drinking water. Warning: Not for human use. Store at controlled room temperature 20° to 25° C (68° to 77°F Important: Chickens should consume water at the following approximate rate to insure intake of the required dose of lincomycin-spectomycin indicated: Broiler and Layer Replacements (Light and Heavy) Age (Weeks) - 1 Daily Water Intake Gallons/1000 - 5 Dosage Mg Antibiotic/Lb - 50-65 Dosage: Provide 2 grams antibiotic activity per gallon of drinking water. Administer as the sole source of water for the first 5 to 7 days of life. Administration: Amount of L-S 50 Amount of Drinking Water 1 bottle - 25 gallons For proportioners delivering 1 ounce of solution per gallon of drinking water, dissolve contents of 5 bottles in each gallon of proportioner solution. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE LS50 75 gram LS-50 Water Soluble Powder is for use in chickens up to 7 days old to help control chronic respiratory disease (CRD). Lincomycin Spectinomycin Water Soluble Powder contains 16.7 gm ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE MalAcetic(R) Ultra Otic For ear cleaning and use as a drying agent in dogs, cats and horses with inflamed and infected ears due to bacteria and/or fungi (yeast). Ceramides aid in moisturizing, repairing, and restoring dry, damaged skin. Features: Broad Spectrum Cleanser A multicleanse flush for topical, antifungal, and antibacterial use for dogs, cats and horses To assist with cleaning and to promote drying the ear during an active ear infection Item Specifications: For Use: In Dogs, Cats, and Horses Size: 8 oz. Active ingredients: Boric acid: 2.0% Acetic Acid: 2.0% Hydrocortisone: 1.0% Ketoconazole ceramides: 0.15% Inactive Ingredients: Propylene glycol, glycerin, polysorbate, fragrance Manufacturer: Dechra Veterinary Products Directions for Use: SHAKE WELL. Apply to the ear canal and gently, but firmly, massage the base of the ear. Use a cotton ball to remove excess solution. Repeat as necessary or as directed by your veterinarian. Close cap tightly. Caution: For topical use only Avoid contact with eyes If skin irritation develops or increases, stop use and call your veterinarian. Keep out of the reach of children and pets. Wash hands after use. Storage: Store at controlled room temperature of 15 - 30° C (59 - 86° F). « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE MalAcetic(R) Ultra Otic For ear cleaning and use as a drying agent in dogs, cats and horses with inflamed and infected ears due to bacteria and/or fungi (yeast). Ceramides aid in moisturizing, ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Local Anesthetic Lidocaine is a potent local anesthetic for producing epidural, nerve conduction and infiltration anesthesia. Lidocaine is contraindicated in animals with a known hypersensitivity to the drug. Lidocaine is usually well tolerated. Nevertheless, as with all local anesthetics, untoward effects may occur due to hypersensitivity, faulty technique, overdosage and inadvertent intravascular or subarachnoid injection. In case of respiratory arrest, immediate resuscitation with oxygen is indicated. Dosage and Administration Epidural Cattle and Horses- 5 to 15 mL Dogs and Cats- 1 mL per 10 pounds Nerve Block Cattle and Horses- 5 to 20 mL. Each mL contains : Lidocaine Hydrochloride 2.0% Propylene Glycol 5.2% Sodium Chloride 0.5% Sodium Lactate 0.5% with Methylparaben 0.15%, Sodium Metabisulfite 0.10%, Propylparaben 0.03% and Disodium Edetate 0.001% as preservatives. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Local Anesthetic Lidocaine is a potent local anesthetic for producing epidural, nerve conduction and infiltration anesthesia. Lidocaine is contraindicated in animals with a known hypersensitivi ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Draxxin Injectable Solution 100 ml Cattle: DRAXXIN Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) ssociated with Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni (Haemophilus somnus), and for the control of respiratory disease in cattle at high risk of developing BRD associated with Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni (Haemophilus somnus). Swine: DRAXXIN Injectable Solution is indicated for the treatment of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica, and Haemophilus parasuis. Dosage: Each ml contains 100 mg tulathromycin. The usual recommended dosage of Draxxin is 2.5 mg per kg (1.1 ml per 100 lbs) body weight, given in the neck. Do not administer more than 10 ml SQ per injection site in cattle. One dose provides up to 7-14 days BRD treatment and control. Do not administer more than 5 ml IM per injection site in swine. Not for use in female dairy cattle 20 months of age or older, or in calves to be processed for veal. Tulathromycin. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Draxxin Injectable Solution 100 ml Cattle: DRAXXIN Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) ssociated with Mannheimia haemolytica, Pasteurella mult ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Naxcel is a broad spectrum injectable antibiotic used in the treatment of multiple species of animals. Naxcel is indicated for the treatment of respiratory disease in cattle, swine, sheep, goats and horses. In cattle, Naxcel is indicated for treatment of bovine respiratory disease (shipping fever, pneumonia) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni . Dosage: For intramuscular and subcutaneous injection in cattle only. For intramuscular injection in swine, sheep, goats and horses. For subcutaneous injection only in dogs, day-old chickens and day-old turkey poults. This product may be used in lactating dairy cattle, sheep and goats. Active Ingredient: Ceftiofur Sodium For intramuscular and subcutaneous injection in cattle only. For intramuscular injection in swine, sheep, goats and horses. For subcutaneous injection only in dogs, day-old chickens and day-old turkey poults. This product may be used in lactating dairy cattle, sheep and goats. Contraindications As with all drugs, the use of NAXCEL Sterile Powder is contraindicated in animals previously found to be hypersensitive to the drug. Warnings NOT FOR HUMAN USE. KEEP OUT OF REACH OF CHILDREN. Penicillins and cephalosporins can cause allergic reactions in sensitized individuals. Topical exposure to such antimicrobials, including ceftiofur, may elicit mild to severe allergic reactions in some individuals. Repeated or prolonged exposure may lead to sensitization. Avoid direct contact of the product with the skin, eyes, mouth, and clothing. Persons with a known hypersensitivity to penicillin or cephalosporins should avoid exposure to this product. In case of accidental eye exposure, flush with water for 15 minutes. In case of accidental skin exposure, wash with soap and water. Remove contaminated clothing. If allergic reaction occurs (e.g., skin rash, hives, difficult breathing), seek medical attention. Storage Conditions Store unreconstituted product at controlled room temperature 20° to 25° C (68° to 77° F) [see USP]. Store reconstituted product either in a refrigerator 2° to 8° C (36° to 46° F) for up to 7 days or at controlled room temperature 20° to 25° C (68° to 77° F) [see USP] for up to 12 hours. Protect from light. Color of the cake may vary from off-white to a tan color. Color does not affect potency « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Naxcel is a broad spectrum injectable antibiotic used in the treatment of multiple species of animals. Naxcel is indicated for the treatment of respiratory disease in cattle, swine, sheep, goat ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Tylovet Soluble Powder Tylovet soluble powder is for use in chickens, turkeys, swine and honey bees only. Equivalent to 100 g tylosin base. Chickens: As an aid in the treatment of chronic respiratory disease (CRD) associated with Mycoplasma gallisepticum in broiler and replacement chickens; and for the control of CRD associated with Mycoplasma gallisepticum at the time of vaccination or other stress in chickens. For control of CRD associated with Mycoplasma synoviae in broiler chickens. Turkeys: For maintaining weight gain and feed efficiency in the presence of infectious sinusitis associated with Mycoplasma gallisepticum. Swine: For the treatment and control of swine dysentery associated with Brachyspira hyodysenteriae. Honey Bees: For the control of American Foulbrood (Paenibacillus larvae). « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Tylovet Soluble Powder Tylovet soluble powder is for use in chickens, turkeys, swine and honey bees only. Equivalent to 100 g tylosin base. Chickens: As an aid in the treatment of chronic respi ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Lutalyse Injection Lutalyse is used as a luteolytic agent in cattle, for parturition induction in swine, and for its luteolytic effect in mares. Lutalyse is indicated for estrus synchronization, treatment of unobserved (silent) estrus and pyometra (chronic endometritis) in cattle; for parturition induction in swine; and for controlling the timing of estrus in estrous cycling mares and clinically anestrous mares that have a corpus luteum. Lutalyse Sterile Solution is supplied at a concentration of 5 mg dinoprost per ml. Dinoprost tromethamine. Active Ingredients: Each mL contains dinoprost tromethamine equivalent to 5 mg dinoprost: also, benzyl alcohol, 9.45 mg added as preservative. Storage: Store at controlled room temperature 20° to 25°C (68° to 77°F) [see USP]. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Lutalyse Injection Lutalyse is used as a luteolytic agent in cattle, for parturition induction in swine, and for its luteolytic effect in mares. Lutalyse is indicated for estrus synchronization ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Lactated Ringer 5% Dextrose Lactated Ringer's Injection 5% Dextrose, USP Rx is a sterile, nonpyrogenic solutions each containing isotonic concentrations of electrolytes (with or without dextrose) in water for injection. The solutions containing dextrose and electrolytes are hypertonic; those containing only electrolytes are isotonic. They are administered by intravenous infusion for parenteral replacement of extracellular losses of fluid and electrolytes, with or without minimal carbohydrate calories. The solutions contain no bacteriostat, antimicrobial agent or added buffer (except for pH adjustment) and each is intended only for use as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid, nutrient and/or electrolyte replenishers. Dosage and Administration: The dose is dependent upon the age, weight and clinical condition of the patient. As reported in the literature, the dosage and constant infusion rate of intravenous dextrose must be selected with caution in pediatric patients, particularly neonates and low birth weight infants, because of the increased risk of hyperglycemia/hypoglycemia. Drug Interactions: Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store. The presence of calcium limits their compatibility with certain drugs that form precipitates of calcium salts, and also prohibits their simultaneous infusion through the same administration set as blood because of the likelihood of coagulation. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. See PRECAUTIONS. Instructions for Use: To Open: Tear outer wrap at notch and remove solution container. If supplemental medication is desired, follow directions below before preparing for administration. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. To Add Medication 1. Prepare additive port. 2. Using aseptic technique and an additive delivery needle of appropriate length, puncture resealable additive port at target area, inner diaphragm and inject. Withdraw needle after injecting medication. 3. The additive port may be protected by covering with an additive cap. 4. Mix container contents thoroughly. Preparation for Administration (Use aseptic technique) 1. Close flow control clamp of administration set. 2. Remove cover from outlet port at bottom of container. EN-2203 Page 5 of 5 3. Insert piercing pin of administration set into port with a twisting motion until the set is firmly seated. NOTE: See full directions on administration set carton. 4. Suspend container from hanger. 5. Squeeze and release drip chamber to establish proper fluid level in chamber. 6. Open flow control clamp and clear air from set. Close clamp. 7. Attach set to venipuncture device. If device is not indwelling, prime and make venipuncture. 8. Regulate rate of administration with flow control clamp. Ingredients: Each 100 mL of Lactated Ringer's and 5% Dextrose Injection, USP contains dextrose, hydrous 5 g plus the same ingredients and mEq values as Lactated Ringer's Injection, USP (contains only hydrochloric acid for pH adjustment). A liter provides 179 calories (from dextrose and lactate) and has a hypertonic osmolar concentration of 525 mOsmol (calc.). The pH is 4.9 (4.0 - 6.5). Contraindications: Solutions containing dextrose may be contraindicated in patients with known allergy to corn or corn products. Warnings: Lactated Ringer's and 5% Dextrose Injection USP should be used with great care if at all in patients with congestive heart failure severe renal insufficiency and in clinical states in which there exists edema with sodium retention. Lactated Ringer's and 5% Dextrose Injection USP should be used with great care if at all in patients with hyperkalemia severe renal failure and in conditions in which potassium retention is present. Lactated Ringer's and 5% Dextrose Injection USP should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions such as severe hepatic insufficiency. Lactated Ringer's and 5% Dextrose Injection USP should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation. The intravenous administration of Lactated Ringer's and 5% Dextrose Injection USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations overhydration congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injection. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injection. In patients with diminished renal function administration of Lactated Ringer's and 5% Dextrose Injection USP may result in sodium or potassium retention. Lactated Ringer's and 5% Dextrose Injection USP is not for use in the treatment of lactic acidosis. Precautions: Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations and acid-base balance during prolonged parenteral therapy or whenever the condition of the patient warrants such evaluation. Solutions containing dextrose should be used with caution in patients with known subclinical or overt diabetes mellitus. Caution must be exercised in the administration of parenteral fluids, especially those containing sodium ions, to patients receiving corticosteroids or corticotropin. Potassium containing solutions should be used with caution in the presence of cardiac disease, particularly in digitalized patients or in the presence of renal disease. Solutions containing lactate ions should be used with caution as excess administration may result in metabolic alkalosis. Do not administer unless solution is clear and container is undamaged. Discard unused portion. Pregnancy Category C. Animal reproduction studies have not been conducted with Ringer's Injection, USP, Ringer's and Dextrose Injection, USP, Lactated Ringer's Injection, USP or Lactated Ringer's and Dextrose Injection, USP. It is also not known whether these injections can cause fetal harm when EN-2203 Page 4 of 5 administered to a pregnant woman or can affect reproduction capacity. These injections should be given to a pregnant woman only if clearly needed. Pediatric Use: The safety and effectiveness in the pediatric population are based on the similarity of the clinical conditions of the pediatric and adult populations. In neonates or very small infants the volume of fluid may affect fluid and electrolyte balance. Frequent monitoring of serum glucose concentrations is required when dextrose is prescribed to pediatric patients, particularly neonates and low birth weight infants. In very low birth weight infants, excessive or rapid administration of dextrose injection may result in increased serum osmolarity and possible intracerebral hemorrhage. Adverse Reactions: Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia. If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Lactated Ringer 5% Dextrose Lactated Ringer's Injection 5% Dextrose, USP Rx is a sterile, nonpyrogenic solutions each containing isotonic concentrations of electrolytes (with or without dextros ...Read more »

Prescription items are NON-RETURNABLE and NON REFUNDABLE Phenylbutazone Bolus 1 gm Tablet Phenylbutazone Bolus is for the relief of inflammatory conditions associated with the musculoskeletal system in horses. A non-hormonal anti-inflammatory agent. DOSAGE & ADMINISTRATION: For horses only. HORSES: Orally - 1 to 2 tablets per 500 lb. body weight. DO NOT EXCEED 4 GRAMS DAILY. Reduce dosage as symptoms regress. Intermittent treatment given only when symptoms appear may be indicated. Contraindications Use with caution in patients who have a history of drug allergy. PRECAUTION: In the treatment of inflammatory conditions associated with infections, specific anti-infective therapy should be used concurrently. Warning Not for use in horses intended for food. Caution Federal law restricts this drug to use by or on the order of a licensed veterinarian. Storage Store at controlled room temperature between 15°-30°C (59°-86°F). Keep container tightly closed when not in use. « Read less

Prescription items are NON-RETURNABLE and NON REFUNDABLE Phenylbutazone Bolus 1 gm Tablet Phenylbutazone Bolus is for the relief of inflammatory conditions associated with the musculoskeletal system in horses. A non-hormonal anti-inflammatory agent. ...Read more »