ISO 9001:2000 Certified |

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Maxef (Ceftriaxone) Composition: Vials containing dry substance equivalent to 250mg, 500mg, 1g Ceftriaxone. Indications: Infections caused by pathogens sensitive to Maxef (Ceftriaxone), e.g.: sepsis,meningitis; abdominal infections (Peritonitis, infections of the biliary and gastrointestinal tracts); infections of the bones, joints, soft tissue, skin and of wounds; infections in patients with impaired defence mechanisms; renal and urinary tract infections; respiratory tract infections, particularly pneumonia, and ear, nose and throat infections; genital infections, including gonorrhea. preoperative prophylaxis of infections. Availabilty: Maxef I.M. injection containing: 1 vial with sterile ceftriaxone sodium U.S.P. equivalent to 250mg, 500mg and 1g ceftriaxone, and 1 ampoule 2ml & 3.5ml of 1 % w/v Lignocaine Hydrochloride solution. Maxef I.V. injection containing: 1 vial with sterile ceftriaxone sodium U.S.P. equivalent to 250mg, 500mg and 1g ceftriaxone, and 1 ampoule 5ml & 10ml of sterile Water for injection.
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