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