CEFUROXIME AXETIL tablet ABD - İngilizce - NLM (National Library of Medicine)

cefuroxime axetil tablet

denton pharma, inc. dba northwind pharmaceuticals - cefuroxime axetil (unii: z49qdt0j8z) (cefuroxime - unii:o1r9fj93ed) - cefuroxime 500 mg - cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (13 years and older) with mild-to-moderate pharyngitis/tonsillitis caused by susceptible strains of streptococcus pyogenes . limitations of use - the efficacy of cefuroxime axetil tablets in the prevention of rheumatic fever was not established in clinical trials. - the efficacy of cefuroxime axetil tablets in the treatment of penicillin-resistant strains of streptococcus pyogenes has not been demonstrated in clinical trials. cefuroxime axetil tablets are indicated for the treatment of pediatric patients (who can swallow tablets whole) with acute bacterial otitis media caused by susceptible strains of streptococcus pneumoniae, haemophilus influenzae (including β-lactamase–producing strains), moraxella catarrhalis (including β-lactamase–producing strains), or streptococcus pyogenes . cefuroxime axetil tablets are indicated for the tr

Cefuroxime Actavis Yeni Zelanda - İngilizce - Medsafe (Medicines Safety Authority)

cefuroxime actavis

teva pharma (new zealand) limited - cefuroxime sodium 1578mg equivalent to cefuroxime 1500 mg;   - powder for injection - 1.5 g - active: cefuroxime sodium 1578mg equivalent to cefuroxime 1500 mg   - cefuroxime is a bactericidal cephalosporin antibiotic which is resistant to most ?-lactamases and is active against a wide range of gram-positive and gram-negative organisms. it is indicated for the treatment of infections before the infecting organism has been identified or when caused by sensitive bacteria. susceptibility to cefuroxime sodium will vary with geography and time and local susceptibility data should be consulted where available. indications include:

Cefuroxime Actavis Yeni Zelanda - İngilizce - Medsafe (Medicines Safety Authority)

cefuroxime actavis

teva pharma (new zealand) limited - cefuroxime sodium 789mg equivalent to cefuroxime 750 mg;   - powder for injection - 750 mg - active: cefuroxime sodium 789mg equivalent to cefuroxime 750 mg   - cefuroxime is a bactericidal cephalosporin antibiotic which is resistant to most ?-lactamases and is active against a wide range of gram-positive and gram-negative organisms. it is indicated for the treatment of infections before the infecting organism has been identified or when caused by sensitive bacteria. susceptibility to cefuroxime sodium will vary with geography and time and local susceptibility data should be consulted where available. indications include:

Zinacef 1.5 g Powder for Solution for Injection or Infusion İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 1.5 g powder for solution for injection or infusion

glaxosmithkline (ireland) limited - cefuroxime sodium - powder for solution for injection/infusion - 1.5 gram(s) - second-generation cephalosporins; cefuroxime

Zinacef 1.5 g Powder for Solution for Injection or Infusion İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 1.5 g powder for solution for injection or infusion

sandoz pharmaceuticals d.d. - cefuroxime sodium - powder for solution for injection/infusion - second-generation cephalosporins; cefuroxime

CEFUROXIME PANPHARMA 750 MG İsrail - İngilizce - Ministry of Health

cefuroxime panpharma 750 mg

pharmalogic ltd - cefuroxime as sodium - powder for solution for inj/inf - cefuroxime as sodium 750 mg/vial - cefuroxime - cefuroxime - infections caused by susceptible microorganisms, prophylaxis against post operative infections in a variety of operations.

Zinacef 250 mg Powder for Solution or Suspension for Injection İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 250 mg powder for solution or suspension for injection

glaxosmithkline (ireland) limited - cefuroxime sodium - powder for solution for injection - 250 milligram(s) - second-generation cephalosporins; cefuroxime

Zinacef  750 mg Powder for Solution or Suspension for Injection İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 750 mg powder for solution or suspension for injection

glaxosmithkline (ireland) limited - cefuroxime sodium - powder for solution for injection - 750 milligram(s) - second-generation cephalosporins; cefuroxime

Zinacef  750 mg Powder for Solution or Suspension for Injection İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 750 mg powder for solution or suspension for injection

sandoz pharmaceuticals d.d. - cefuroxime sodium - powder for solution for injection - second-generation cephalosporins; cefuroxime

Zinacef 250 mg Powder for Solution or Suspension for Injection İrlanda - İngilizce - HPRA (Health Products Regulatory Authority)

zinacef 250 mg powder for solution or suspension for injection

sandoz pharmaceuticals d.d. - cefuroxime sodium - powder for solution for injection - second-generation cephalosporins; cefuroxime