Clindamycin is an antibiotic belonging to the Lincosamide group, which is a semi-synthetic modification of Lincomycin. It has an action spectrum similar to Erythromycin, i.e., gram-positive bacteria, especially staphylococci, streptococci and anaerobic bacteria. Lincosamides are useful for the treatment of infections resistant to Penicillin, Erythromycin and Cephalosporins. Clindamycin inhibits bacterial protein synthesis, altering translocation. It binds to the 50S subunit of the bacterial ribosome, preventing the translocation of transfer RNA from the A site to the P site of the ribosome, preventing the formation of peptide bonds and generating the inhibition of protein synthesis of the microorganism. Each 620 mg tablet contains: Clindamycin Hydrochloride..............195.04 mg (Equivalent to 165 mg of Clindamycin base) Excipients q.s.p...........................620 mg
Place of origin
Chile
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