A bacteriostatic broad-spectrum antibiotic disrupts protein synthesis in a microbial cell (having fat-solubility, penetrates through the bacterial cell membrane and reversibly binds to the subunit 50S bacterial ribosomes, in which the movement of amino acids to growing peptide chains is delayed, which leads to a violation of protein synthesis). It is effective against strains of bacteria that are resistant to penicillin, tetracycline, sulfonamides. Active with respect to Neisseria gonorrhoeae, Chlamydia trachomatis, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, some species Enterobacter and Neisseria, Staphylococcus aureus, Streptococcus spp. (at t.ch.. Streptococcus pneumoniae, Streptococcus haemolyticus), Moraxella lacunata, rickettsia and mycoplasmas.
Ineffective against acid-fast bacteria, anaerobes, Acinetobacter spp., Serratia marcescens.