Tilmicosin Premix, Tilmicosin Oral Solution & Tilmicosin Phosphate Injection

China Tilmicosin Premix, Tilmicosin Oral Solution & Tilmicosin Phosphate Injection, Find details about China Tilmicosin 20% Premix, on Factory Price from Tilmicosin Premix, Tilmicosin Oral Solution & Tilmicosin Phosphate Injection

Basic Info.

Trademark

CHBT

Specification

100g or customized

Origin

Henan China

Trademark

CHBT

Specification

100g or customized

Origin

Henan China

Product Desciption

Tilmicosin (as tilmicosin phosphate) Premix 200 g/kg

FOR VETERINARY USE ONLY / ANTIBIOTIC

For use in swine, feedlot cattle and rabbit feeds only - must be thoroughly mixed in feeds before use.

Active Ingredient

Tilmicosin (as tilmicosin phosphate)

200 g/kg

Tilmicosin 20% Premix Indications

1. As an aid in reducing the severity of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae and Pasteurella multocida when fed to pigs approximately 7 days prior to an anticipated disease outbreak.
2. As an aid in reducing the severity of porcine polyserositis and arthritis associated with Haemophilus parasuis (Glasser's Disease) when fed to pigs approximately 7 days prior to an anticipated disease outbreak.
3. For the reduction of bovine respiratory disease (BRD) morbidity associated with Mannheimia haemolytica, Pasteurella multocida and/or Histophilus somni in groups of feedlot beef cattle experiencing an outbreak of BRD.
4. For the reduction in severity of respiratory disease caused by Pasteurella multocida in rabbits.

Note: To promote responsible use and limit the development of antimicrobial resistance, use Tilmicosin 20% premix only under the following conditions:

1 In swine when factors associated with outbreaks of SRD or Glasser's Disease (such as herd health status, target pig population, herd management and environmental factors, etc.) have been carefully considered.
2 In feedlot beef cattle when:
a) clinical BRD has been diagnosed in at least 10% of animals in the group to be treated; AND
b) treatment is initiated within the first 45 days of arrival in the feedlot; AND
c) medication is limited to one single period of 14 consecutive days of treatment.

Dosage and Administration

To reduce the development of antimicrobial resistance and maintain effectiveness, use this antibiotic prudently and for the shortest duration required to achieve the desired clinical outcome.
Swine
Indication 1: Feed at 200 g tilmicosin activity per tonne (1000 kg) for a 21 day period, beginning approximately 7 days before an anticipated outbreak. Feed continuously as the sole ration.
To provide 200 g tilmicosin activity per tonne (1000 kg) in complete feed, thoroughly mix 1.0 kg of Tilmicosin 20% Premix  into 999 kg non-medicated swine feed.
Indication 2: Feed at 400 g tilmicosin activity per tonne (1000 kg) for a 21 day period, beginning approximately 7 days before an anticipated outbreak. Feed continuously as the sole ration.
To provide 400 g tilmicosin activity per tonne (1000 kg) in complete feed, thoroughly mix 2.0 kg Tilmicosin 20% Premix  into 998 kg non-medicated swine feed.

Beef Cattle

Indication 3: Feed at the appropriate concentration in medicated feed to target 12.5 mg/kg body weight/head/day for a 14 day period.
Tilmicosin 20% Premix  should be blended into an intermediate mix (premix or supplement) to supply 12.5 mg per kg of body weight (BW) and then mixed into the complete diet (total mixed ration [TMR]). Feed continuously in the complete diet (TMR) of cattle.
The following is the calculation to determine the concentration of tilmicosin in the complete feed and intermediate mix:
I. Calculate the amount (mg) of tilmicosin activity required per head per day.
  Body weight (kg) x 12.5 mg/kg BW
II. Calculate the dry matter intake (DMI) in kg per head per day.
  Body weight (kg) x estimated DMI as a percent of BW
III. Calculate the concentration (mg/kg) in the complete diet (TMR).
Amount (mg) of tilmicosin required per head per day divided by the DMI (kg)
IV. Calculate the concentration of tilmicosin in the intermediate mix (mg/kg = g /tonne).
  Concentration in the complete diet (mg/kg) divided by the intended inclusion rate (%) of the intermediate mix in the complete diet
V. Calculate the amount of Tilmicosin 20% Premix  to be added per tonne (1000 kg) of the intermediate mix.
Concentration of tilmicosin (g/tonne) in the intermediate mix divided by the TILMICOSIN 200 concentration (200 g tilmicosin per kg)

An example: Body weight is 300 kg; Dry matter intake as a percent of body weight is 2%; Intermediate premix or supplement is to be incorporated in the complete feed at 4% of dry matter.
1. 300 kg x 12.5 mg/kg = 3750 mg tilmicosin per head per day
2. 300 kg x 2% (or 300 x 0.02. = 6 kg dry matter intake per head per day
3. 3750 mg tilmicosin per head per day divided by 6 kg DMI = 625 mg tilmicosin/kg DMI
4. 625 mg/kg divided by 4% inclusion (or 625 mg/kg divided by 0.04) = 15,625 mg/kg or 15,625 g/tonne tilmicosin in the intermediate mix
5. 15,625 g/tonne tilmicosin in the intermediate mix divided by 200 g tilmicosin per kg TILMICOSIN 200 =78.125 kg/tonne

Rabbits
Indication 4: Tilmicosin 20% Premix should be blended into an intermediate mix (premix or supplement) and then mixed into the complete diet (total mixed ration [TMR]) to supply 12.5 mg tilmicosin per kg of body weight (BW), equivalent to 200 ppm in feed for 7 days. This is achieved by the incorporation of 1 kg Tilmicosin 20% Premix per tonne of feed. Feed continuously as the sole ration.

Contraindications

1. Do not use in animals hypersensitive to tilmicosin.
2. Tilmicosin is known to be toxic for horses. Do not allow horses or other equines access to feeds containing tilmicosin.

CAUTIONS:
1. The safety of tilmicosin has not been established in boars used for breeding.
2. The effects of tilmicosin on bovine reproductive performance, pregnancy and lactation have not been determined.
3. The effects of tilmicosin on rabbit reproductive performance, pregnancy and lactation have not been determined.
4. The safety of tilmicosin in pre-ruminant calves has not been established.
5. Do not use in any feed (supplement, concentrate or complete feed) containing bentonite. Bentonite in feeds may affect the efficacy of tilmicosin.

Warnings

1. Treated animals must not be slaughtered for use in food for at least 14 days for swine, 28 days for cattle, and 4 days for rabbits after the latest treatment with this drug.
2. Do not use in lactating dairy cattle.
3. To limit the development of antimicrobial resistance, Tilmicosin 20% Premix should only be used in swine at high risk of developing SRD or Glasser's Disease and in feedlot beef cattle at high risk of developing BRD.
4. When mixing and handling Tilmicosin 20% Premix , wear protective clothing, impervious gloves, and a dust mask. Operators should wash thoroughly with soap and water after handling. If accidental eye contact occurs, immediately rinse thoroughly with water, if irritation persists, seek medical attention.
5. Keep out of reach of children.
6. To report adverse effects in users or to obtain occupational safety information, call 1-800-265-1763.