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Swine Intestinal Integrity

Intestinal Integrity Solutions

Elanco offers vaccine, injectable, feed and water soluble solutions for industry-critical intestinal integrity challenges.

Swine Respiratory Health

Respiratory Health Solutions

Elanco offers vaccine, injectable, feed and water soluble solutions for industry-critical respiratory challenges.

Swine Vaccines

Vaccine Solutions

Elanco offers vaccine solutions for industry-critical diseases.

Productivity Solutions

Manage profit potential with flexible and consistent finishing improvement.

Insecticide Solutions

Target pests the right way with a broad portfolio of chemical classes, modes of action and operational applications.

How to Contact Us

Contact your Elanco representative to find the right solutions for your operation.

The labels contain complete use information, including cautions and warnings. Always read, follow and understand the label and use directions.


PULMOTIL® AC

IMPORTANT SAFETY INFORMATION:

Before using this product, it is important to read the entire product insert, including the boxed human warning.

WARNING: Exposure to tilmicosin in humans has been associated with chest pain, increased heart rate, dizziness, headache, and nausea. Death has been reported following ingestion or injection of tilmicosin. Avoid direct skin and eye contact. In case of human exposure, call 1-800-722-0987 and consult a physician immediately.

  • Wear overalls, impervious gloves and eye protection when mixing and handling the product. Wash hands after handling the product. Wash affected parts if skin contact occurs. If accidental eye contact occurs, immediately rinse thoroughly with water.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

  • For use only in swine. Not for injection. Injection of tilmicosin has been shown to be fatal in swine and non-human primates, and may be fatal in horses and goats.
  • Swine intended for human consumption must not be slaughtered within 7 days of treatment.
  • Always treat the fewest number of animals necessary to control a respiratory disease outbreak. Prescriptions shall not be refilled.
  • Concurrent use of Pulmotil AC and another macrolide by any route, or use of another macrolide immediately following this use of Pulmotil AC is not advised.
  • Ensure that pigs have continuous access to medicated water during the treatment period. Monitor pigs for signs of water refusal and dehydration while being treated.

INDICATIONS:

  • For the control of swine respiratory disease associated with Pasteurella multocida and Haemophilus parasuis in groups of swine in buildings where a respiratory disease outbreak is diagnosed.
  • For the control of swine respiratory disease associated with Mycoplasma hyopneumoniae in the presence of porcine reproductive and respiratory syndrome virus (PRRSv) in groups of swine in buildings where a respiratory disease outbreak is diagnosed.

DOSAGE AND ADMINISTRATION:

  • Must be diluted before administration to animals.
  • Include in the drinking water to provide a concentration of 200 mg tilmicosin per liter (200 ppm).
  • One 960 ml bottle is sufficient to medicate 1200 liters (320 gallons) of drinking water for pigs.
  • The medicated water should be administered for (5) five consecutive days.
  • Use within 24 hours of mixing with water.
  • Do not use rusty containers for medicated water as they may affect product integrity.
  • When using a water medicating pump with a 1:128 inclusion rate, add 1 bottle (960 ml) of Pulmotil AC per 2.5 gallons of stock solution.


DENAGARD® 10 PREMIX

INDICATIONS: 

  • For treatment of swine dysentery associated with Brachyspira (formerly Serpulina or Treponema) hyodysenteriae susceptible to Tiamulin
  • For control of porcine proliferative enteropathies (ileitis) associated with Lawsonia intracellularis
  • For control of swine dysentery associated with Brachyspira (formerly Serpulina or Treponema) hyodysenteriae susceptible to Tiamulin

DIRECTIONS FOR USE

  • For treatment of swine dysentery associated with Brachyspira (formerly Serpulina or Treponema) hyodysenteriae susceptible to Tiamulin
    • Amount of Type B Medicated Feed Per Ton of Feed: 20 lb
    • Tiamulin hydrogen fumarate in Complete Type C Medicated Feed Per Ton: 200 g
    • Withdrawal Period (days): 7
  • For control of porcine proliferative enteropathies (ileitis) associated with Lawsonia intracellularis
    • Amount of Type B Medicated Feed Per Ton of Feed: 3.5 lb
    • Tiamulin hydrogen fumarate in Complete Type C Medicated Feed Per Ton: 35 g
    • Withdrawal Period (days): 2
  • For control of swine dysentery associated with Brachyspira (formerly Serpulina or Treponema) hyodysenteriae susceptible to Tiamulin
    • Amount of Type B Medicated Feed Per Ton of Feed: 3.5 lb
    • Tiamulin hydrogen fumarate in Complete Type C Medicated Feed Per Ton: 35 g
    • Withdrawal Period (days): 2

IMPORTANT SAFETY INFORMATION

  • Keep out of reach of children. 
  • Avoid contact with skin. Direct contact with skin or mucous membranes may cause irritation. 

CAUTION: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian. Do not feed undiluted. Do not use in feeds for animals other than swine.

  • The effects of Tiamulin on swine reproductive performance, pregnancy and lactation have not been determined. 
  • Swine being treated with Denagard (Tiamulin) should not have access to feeds containing polyether ionophores (e.g., lasalocid, monensin, narasin, salinomycin and semduramicin) as adverse reactions may occur. If signs of toxicity occur, discontinue use.


PRADALEXTM

INDICATIONS:

  • Pradalex is indicated for the treatment of SRD associated with Bordetella bronchiseptica, Glaesserella (Haemophilus) parasuis, Pasteurella multocida, Streptococcus suis, and Mycoplasma hyopneumoniae in weaned swine intended for slaughter (nursery, growing, and finishing swine, boars intended for slaughter, barrows, gilts intended for slaughter, and sows intended for slaughter).
  • Not for use in swine intended for breeding (boars intended for breeding, replacement gilts, and sows intended for breeding) and in nursing piglets.

DOSAGE AND ADMINISTRATION:

  • Administer once as an intramuscular injection in the neck at a dosage of 7.5 mg/kg
  • (1.7 mL/100 lb) body weight. Do not inject more than 5 mL per intramuscular injection site.

IMPORTANT SAFETY INFORMATION:

  • Federal law restricts this drug to use by or on the order of a licensed veterinarian.
  • Federal law prohibits the extra-label use of this drug in food-producing animals.
  • To ensure responsible antimicrobial drug use, use of pradofloxacin should be limited to treatment of bovine respiratory disease (BRD) in cattle and treatment of swine respiratory disease (SRD) in swine only after consideration of other non-fluoroquinolone therapeutic options.


PREVACENT® PRRS

INDICATIONS:

  • This product has been shown to be effective for the vaccination of healthy pigs 2 weeks of age or older against PRRS respiratory disease; and against reproductive disease when vaccinated 6 weeks prior to breeding.
  • The duration of immunity against respiratory disease is at least 26 weeks.
  • The duration of immunity against reproductive disease has not been established. For more information regarding efficacy and safety data, go to productdata.aphis.usda.gov.
  • Safety of this product has been demonstrated when sows or gilts are vaccinated prior to breeding or at any stage of pregnancy.
  • Vaccine virus may be shed and transmitted to other populations of swine in contact with vaccinated swine.
  • The duration of potential vaccine virus transmission may vary.
  • Use of the vaccine in herds intended to remain PRRS virus seronegative is contraindicated.
  • Introduction of vaccinated pigs into herds intended to remain PRRS virus seronegative is contraindicated.

DOSAGE AND ADMINISTRATION:

  • Rehydrate with the accompanying sterile diluent.
  • Shake well and draw back into the syringe the required amount.
  • Administer 1 mL intramuscularly.
  • The need for annual booster vaccinations has not been established for this product; consultation with a veterinarian is recommended.

IMPORTANT SAFETY INFORMATION

PRECAUTIONS:

  • Store at 2°- 8°C (35°- 46°F). DO NOT FREEZE.
  • Use entire contents when first opened.
  • Do not mix with other products, except as specified on this label. In case of human exposure, contact a physician.
  • Do not vaccinate within 21 days before slaughter.
  • Inactivate unused contents before disposal.
  • Anaphylactic reactions may occur. Symptomatic treatment: Epinephrine. Contains gentamicin as preservative.


SKYCIS®

INDICATIONS:

  • For increased rate of weight gain in growing-finishing swine when fed for at least 4 weeks.
  • For increased rate of weight gain and improved feed efficiency in growing-finishing swine when fed for at least 4 weeks.


DIRECTIONS FOR USE:

  • For increased rate of weight gain in growing-finishing swine when fed for at least 4 weeks: Feed 13.6 to 27.2 g/ton (15 ppm to 30 ppm) in a Type C Medicated feed.
  • For increased rate of weight gain and improved feed efficiency in growing-finishing swine when fed for at least 4 weeks: Feed 18.1 to 27.2 g/ton (20 ppm to 30 ppm) in a Type C Medicated feed.
  • No increased benefit in rate of weight gain has been shown when narasin concentrations in the diet are greater than 15 ppm (13.6 g/ton).


IMPORTANT SAFETY INFORMATION

CAUTION:

  • Do not allow adult turkeys, horses or other equines access to narasin formulations. Ingestion of narasin by these species has been fatal. Not approved for use in breeding animals because safety and effectiveness have not been evaluated in these animals.
  • Swine being fed with Skycis (narasin) should not have access to feeds containing pleuromutilins (e.g. tiamulin) as adverse reactions may occur. If signs of toxicity occur, discontinue use.

WARNING: No withdrawal period is required when used according to the label.

  • Store at or below 25° C (77°F). Excursions permitted to 37° C (99°F).


Communicate Skycis inclusions in feed to the full production system prior to use. Proper training, formulations, mixing and concentration levels are important to successfully implement Skycis.

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