The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Active Drug Ingredient
Chlortetracycline calcium complex equivalent to 50 g chlortetracycline hydrochloride per lb.
Aureomycin Granular Type A Medicated Article (Dried Streptomyces aureofaciens Fermentation Product and Calcium Sulfate) and Calcium Carbonate.
Mix sufficient Aureomycin 50 Granular A Medicated Article to supply desired concentration of chlortetracycline per ton with part of the feed ingredients to make a preblend.Add the remainder of the ingredients and mix thoroughly. For specific use levels, see Indications for use.
Level desiredgrams per ton Amount of medicated article per ton † 10 1/5 lb 50 1 lb 100 2 lb 200 4 lb 400 8 lb 500 10 lb† It is recommended that 1 pound of Aureomycin 50 Granular A Type A Medicated Article be diluted with 4 pounds of one of the feed ingredients to form a 5 pound working premix. Use 1 pound of the working premix to make a preblend (see Use directions) for a Type C feed containing 10 g Aureomycin chlortetracycline / ton of feed.
Indications For Use
Indications for use Chlortetracyclinemg per lb bodywt per dayCattle Beef Cattle (over 700 lb): Control of active infection of anaplasmosis caused by Anaplasma marginale susceptible to chlortetracycline. 0.5 Beef and Non-Lactating Dairy Cattle: As an aid in the control of active infection of anaplasmosis caused by Anaplasma marginale susceptible to chlortetracycline when delivered in a free-choice feed. Free-choice feed must be manufactured under a feed mill license utilizing an FDA approved formulation. 0.5-2.0 Calves, Beef and Non-Lactating Dairy Cattle: Treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida organisms susceptible to chlortetracycline. Feed for not more than 5 days. The appropriate amount of Aureomycin-containing feed supplement may be mixed in the cattle's daily ration or administered as a top-dress. If the Aureomycin-containing feed supplement is administered as a top-dress, it must be spread uniformly on top of the ration and sufficient space must be provided so that all cattle can eat at the same time. 10 Swine Control of porcine proliferative enteropathies (ileitis) caused by Lawsonia intracellularis susceptible to chlortetracycline. Treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to chlortetracycline. (Note: this drug level is equivalent to approximately 400 grams per ton, depending on feed consumption and body weight.) Feed for not more than 14 days. 10 Turkeys Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to chlortetracycline. Feed continuously for 7 to 14 days. 25 Indications for use mg per headper dayCattle Growing Cattle (over 400 lb): Increased rate of weight gain, improved feed efficiency, and reduction of liver condemnation due to liver abscesses. 70 Beef Cattle and Dairy Replacement Heifers: Control of bacterial pneumonia associated with shipping fever complex caused by Pasteurella spp. susceptible to chlortetracycline. 350 Beef Cattle (under 700 lb): Control of active infection of anaplasmosis caused by Anaplasma marginale susceptible to chlortetracycline. 350 Sheep Breeding Sheep: Reduction in the incidence of (vibrionic) abortions caused by Campylobacter fetus infection susceptible to chlortetracycline. 80 Indications for use In complete feed Chlortetracycline g per tonSwine Reduction in the incidence of cervical lymphadenitis (jowl abscesses) caused by Group E Streptococci susceptible to chlortetracycline. 50-100 Breeding Swine: Control of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to chlortetracycline. Feed continuously for not more than 14 days. 400 Ducks Control and treatment of fowl cholera caused by Pasteurella multocida susceptible to chlortetracycline. Feed in complete ration to provide from 8 to 28 mg per pound of body weight per day depending upon age and severity of disease. Feed for not more than 21 days. 200-400 Chickens Control of infectious synovitis caused by Mycoplasma synoviae susceptible to chlortetracycline.Feed continuously for 7 to 14 days. 100-200 Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to chlortetracycline.Feed continuously for 7 to 14 days. 200-400 Reduction of mortality due to Escherichia coli infections susceptible to chlortetracycline. Feed for 5 days. 500 Turkeys Control of infectious synovitis caused by Mycoplasma synoviae susceptible to chlortetracycline.Feed continuously for 7 to 14 days. 200 Control of hexamitiasis caused by Hexamita meleagridis susceptible to chlortetracycline.Feed continuously for 7 to 14 days. 400 Turkey Poults not over 4 weeks of age: Reduction of mortality due to paratyphoid caused by Salmonella typhimurium susceptible to chlortetracycline. 400 Indications for use mg per g feedPsittacine birds Warning: Psittacosis, avian chlamydiosis, or ornithosis is a reportable communicable disease, transmissible between wild and domestic birds, other animals and man. Contact appropriate public health and regulatory officials. Caution: Aspergilliosis may occur following prolonged treatment. Treatment of psittacine birds (parrots, macaws, cockatoos) suspected or known to be infected with psittacosis caused by Chlamydia psittaci sensitive to chlortetracycline. Feed continuously for 45 days. Each bird should consume an amount of medicated feed equal to one-fifth of its body weight daily. During treatment, parrots, macaws, and cockatoos should be kept individually or in pairs in clean cages. 10
Withdrawal Periods And Residue Warnings
No withdrawal period is required when used according to labeling. This drug is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. Do not feed to ducks or turkeys producing eggs for human consumption.
Store below 25°C (77°F), excursions permitted to 37°C (99°F)Restricted Drug (California) - Use only as directed. Not for use in humans. Keep out of reach of children.Approved by FDA under NADA # 048-761 zoetisDistributed by:Zoetis Inc.Kalamazoo, MI 4900740025762