Eimicid

Sodium salinomycin

Manufactured using thermostabilizing microgranulation technology that ensures

Stability at heating up to 110°С

Granules homogenicity

Uniform distribution of API in the feed

Low dust formation

Stability at further storage of feed

Description
Drug being a part of MAX-effect anticoccidial program.

Eimicid is gray to gray brown granules.

Packing: 20 kg multi-layered paper bags with PE inlay
Composition
Composition

1 g
Eimicid

120 mg salinomycin
Pharmacological properties
Pharmacological properties

Salinomycin is a fermentation product of Streptomyces albus fungus. It has a broadspectrum anticoccidial action; namely, it is active against: E. necatrix, E. mitis, E. аcervulina, Е. tenella, E. brunetti, E. maxima, E. mivati, E. рraecox, and other coccidia parasites in poultry.

Mode of action: salinomycin disrupts transfer of sodium and potassium cations in immature coccidia, thus causing their death at the stage of schizogony.

Administered orally, Eimicid is poorly absorbed in the gastrointestinal tract and has an anticoccidial action in the mucous membrane and submucosal layer of the intestine. It is excreted from the body in an unchanged form with excrements.
Indications
Indications

Eimicid is prescribed for broilers and replacement chickens to prevent coccidiosis.
Dosage and route of administration
Dosage and route of administration
Eimicid is used mixed with the feed at a dose of 500 g per 1 ton of feed (on API basis — 60 mg of sodium salinomycin per 1 kg of feed, which corresponds to 6 mg of salinomycin sodium per 1 kg of poultry body weight):
- in broiler chickens — introduced on the first day of life for the entire period of rearing and excluded from the diet only 5 days before slaughter
- in replacement chickens — introduced on the first day of life and excluded from the diet 14 days before the egg-laying period starts.
To ensure uniform distribution of the drug throughout the feed, a two stage mixing method is used: the calculated dose of Eimicid is mixed with a little amount (up 10% of a daily portion) of the combined feed and then added to the rest of the combined feed while mixing thoroughly. Added to the combined feed, the drug is stable within 3 months.
Restrictions
Restrictions

CONTRAINDICATIONS

Avoid applying the drug in laying hens and replacement chicks less than 14 days before egg laying starts.

RESTRICTIONS

Treated animals can be slaughtered for human consumption 5 days after the last application of Eimicid. Meat of animals forcedly slaughtered before the established deadlines can be used for feeding carnivores.

SHELF LIFE

3 years from the date of manufacture; after first opening - 3 months

Description
Composition
Pharmacological properties
Indications
Dosage and route of administration
Restrictions

Drug being a part of MAX-effect anticoccidial program.

Eimicid is gray to gray brown granules.

Packing: 20 kg multi-layered paper bags with PE inlay

Composition

1 g

Eimicid

120 mg salinomycin

Pharmacological properties

Salinomycin is a fermentation product of Streptomyces albus fungus. It has a broadspectrum anticoccidial action; namely, it is active against: E. necatrix, E. mitis, E. аcervulina, Е. tenella, E. brunetti, E. maxima, E. mivati, E. рraecox, and other coccidia parasites in poultry.

Mode of action: salinomycin disrupts transfer of sodium and potassium cations in immature coccidia, thus causing their death at the stage of schizogony.

Administered orally, Eimicid is poorly absorbed in the gastrointestinal tract and has an anticoccidial action in the mucous membrane and submucosal layer of the intestine. It is excreted from the body in an unchanged form with excrements.

Indications

Eimicid is prescribed for broilers and replacement chickens to prevent coccidiosis.

Video

Dosage and route of administration

Eimicid is used mixed with the feed at a dose of 500 g per 1 ton of feed (on API basis — 60 mg of sodium salinomycin per 1 kg of feed, which corresponds to 6 mg of salinomycin sodium per 1 kg of poultry body weight):

in broiler chickens — introduced on the first day of life for the entire period of rearing and excluded from the diet only 5 days before slaughter
in replacement chickens — introduced on the first day of life and excluded from the diet 14 days before the egg-laying period starts.

To ensure uniform distribution of the drug throughout the feed, a two stage mixing method is used: the calculated dose of Eimicid is mixed with a little amount (up 10% of a daily portion) of the combined feed and then added to the rest of the combined feed while mixing thoroughly. Added to the combined feed, the drug is stable within 3 months.

Restrictions

CONTRAINDICATIONS

Avoid applying the drug in laying hens and replacement chicks less than 14 days before egg laying starts.

RESTRICTIONS

Treated animals can be slaughtered for human consumption 5 days after the last application of Eimicid. Meat of animals forcedly slaughtered before the established deadlines can be used for feeding carnivores.