DOBUSTAT 250MG INJ.
Dobustat - Dobustat Injection, USP is 1,2-benzenediol, 4-[2-[[3-(4-hydro-xyphenyl)-1-methylpropyl]amino]ethyl]-hydrochloride, (±). It is a synthetic catecholamine. The clinical formulation is supplied in a sterile form for intravenous use only. Each mL contains: Dobustat hydrochloride, equivalent to 12.5 mg (41.5 μmol) Dobustat; 0.24 mg sodium metabisulfite (added during manufacture), and water for injection. pH adjusted between 2.5 to 5.5 with hydrochloric acid and/or sodium hydroxide. Dobustat is oxygen sensitive. Dobustat injection is indicated when parenteral therapy is necessary for inotropic support in the short-term treatment of adults with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures. In patients who have atrial fibrillation with rapid ventricular response, a digitalis preparation should be used prior to institution of therapy with Dobustat hydrochloride. Active ingredients: Dobutamine