SUMMARY
The technological aspects of optimization of production preparation SINARTA for parenteral introduction have been carried out. It is set during experiment, that a production comes true in aseptic terms from sterile initial substances and materials with the use of sterile filtration for an ampoule A and eventual thermal sterilization for the ampoule of B. Reasonable technology of preparation SINARTA for parenteral introduction provides the indexes of quality concordantly pharmacopeias requirements and specifications.