Composition: 1 vial of powder for suspension for injection contains:

Active ingredients:

Benzylpenicillin-potassium 0.63 g

(Equivalent to 1,000,000 IU benzylpenicillin)

Benzilpenicillin-procaine 3.00 g

(In the form of procaine benzylpenicillin-1% lecithin)

(Equivalent to 3,000,000 IU benzylpenicillin)

Indications: Treatment of infections caused by bacteria susceptible to penicillin, which is

made after antibioticogram: infections of the gastrointestinal, respiratory and urogenital

tract, skin and soft tissues.

Contraindications: The drug is not administered to animals hypersensitive to penicillins

and cephalosporins. Also, the composition is not given to pregnant sows and gilts, small

herbivores and sport horses two weeks before the race. The drug is not used in horses

whose meat is intended for human consumption, or in sheep whose milk is used in

human nutrition.

Side effects: In treated animals may develop hypersensitivity reactions (allergy,

anaphylaxis), nerve disorders (excitation, incoordination, ataxia, vomiting) and possible

“vaginal wash” and abortions in sows and gilts.

If you notice serious, or any other side effects not listed here, notify your veterinarian.

Target species:

Cattle, sheep, pigs, horses, dogs and cats.

Dosage and method of administration: Preliminary reconstituted with water for

injection drug is given intramuscularly at a dose, amount:

Horses 25000 IU (0.0625 mL) / kg b.w..

Cattle and pigs 6000-12000 IU (0.015 – 0.03mL) / kg b.w.

Calves and sheep 18000- 36000 IU / (0.045 – 0.09 mL) / kg b.w.

Dogs and cats 25000 IU (0.0625mL) / kg b.w.

1 ml of reconstituted suspension containing 400000 IU

The medicine is applied once a day to cure. The treatment is continued for 3-4 days after

the cessation of the symptoms of the disease.

When the horse’s daily dose should be divided applied at three locations.

Instructions for proper use of drugs: Neo-penicillin should be reconstituted with water

for njection.

For the process of reconstitution are necessary vials with water for injection, a sterile

syringe ogf 10-mL and sterile needle.

Remove the perforated part of the aluminum caps. Into the sterile siringe pull in 10 mL

of water for injection making sure that an excess of entrapped air is pumped out. In the

vial (bottle) of Neo-penicillin displace 10 ml of water for injections through the hole on

the aluminum cap piercing the rubber stopper.

Thereafter a syringe with a needle draws out.

Vial (bottle) shake vigorously until a fine white suspension.

After reconstitution each ml contains 400 000 IU (0.3 g, procaine benzylpenicillin and

0.063 g of potassium Benzilpenicillin).

Reconstituted product is a homogeneous white suspension without lumps

(agglomerates). The product should be rejected immediately if any of the lumps in the


Before using the rubber tip is disinfected with an alcohol swab and a new sterile syringe

and needle to draw the appropriate amount of suspension.

Reconstituted preparation should be used immediately. Unused amount to be rejected

that is disposed of in accordance with applicable regulations.

The drug is administered intramuscularly, does not give i.v.

Broad-spectrum antibiotics and erythromycin reduce the antimicrobial activity of

penicillin. Cephalosporins, polymyxin and aminoglycoside antibiotics enhance the

antimicrobial activity of penicillin. Oxyphenbutazone and probenecid reduces excretion of

penicillin in the kidney. Acids, bases and oxidizing agents rapidly inactivate penicillins.

Penicillin enhances the effect of anticoagulant agents.

Withdrawal period: Meat and edible organs are not for use during the course of

therapy, as well as 16 days in cattle, 9 days in sheep and 7 days in pigs after the last

application of the drug.Milk of cows is not for use during therapy and 3 days after the last

application of the medicine. The drug is not used in horses whose products are used in

human nutrition, as well as in sheep whose milk is used in human nutrition.

Special considerations:

Use in pregnancy and lactation: The drug is not given to sows and gilts, as well as

sheep whose milk is used in human nutrition.

Special considerations for persons administering the veterinary medicinal product

to animals:

In applying the drug should avoid direct contact with skin and mucous membranes, or

eyes.Hands after each application should be washed and medicine kept out of the reach

of children.In the case of the signs of hypersensitivity consult a specialist.

Special precautions for disposal and destruction of drug

Unused drug or drug residues shall be destroyed in accordance with applicable


Special considerations for storing drugs: Store in original container at temperatures

up to 25 ° C, out of reach of children.

Shelf life: 2 years in original packaging.

Shelf life after reconstitution: use immediately.

Packaging: Box of 50 vials x 4 million i.j.

ATCvet code: QJ 01CE30

Method of issue: on prescription of veterinarian

Number and date of registration: 323-01-00583-14-001 date 21.07.2015.

Producer:” FM” Pharm, Subotica, 024/548-130


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