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Guangdong Bozhou Pharmaceutical Co., Ltd.
  • Founded in:

    2000-12-07
  • Country:

    China China
  • Address:

    Green Industrial Park, Jiedong Economic Development Zone, Jieyang City
  • Tax NO.:

    9144520372599310X7
  • Registered Funds:

    20 million yuan
  • Email:

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Cefonicid Sodium for Injection
Cefonicid Sodium
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Cefonicid sodium

This product is a second-generation cephalosporin for intravenous or intramuscular injection. This product has a wider antibacterial spectrum against Gram-negative bacilli than the first-generation cephalosporins. It has good antibacterial activity similar to cefoxitin against Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Citrobacter, Providencia and Enterobacter, but its activity against indole-positive Proteus, Morganella, Providencia and some Klebsiella is lower than that of cefoxitin. It has satisfactory activity against gonococci of influenza bacilli, including beta-lactamase-producing strains. Like other second-generation cephalosporins, Pseudomonas, Serratia and Acinetobacter are resistant to this product. This product is effective against most Gram-positive cocci. Its activity against Staphylococcus aureus is similar to that of cefoxitin and cefuroxime, but lower than that of cefoxitin, cephalothin and cefazolin. 90% of the strains can be inhibited by this product at a concentration of 4.0 to 8.3 mg/L. Most streptococci, including Streptococcus pneumoniae, Streptococcus pyogenes and Group B Streptococcus, are sensitive to this product. Staphylococcus epidermidis is relatively resistant to this product. Streptococcus faecalis, Staphylococcus aureus and methicillin-resistant strains of Staphylococcus epidermidis are all resistant to this product. The activity of this product against anaerobic bacteria has not been well studied, and Bacteroides fragilis is resistant to this product. The minimum bactericidal concentration (MBC) of this product for Staphylococcus aureus, Group B Streptococcus and Escherichia coli is significantly higher than its minimum inhibitory concentration (MIC). This product is very stable to type I beta-lactamase, but can be slowly hydrolyzed by type IIIa, IIIb and V beta-lactamase, while only type IV beta-lactamase is sensitive.

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This product is a second-generation cephalosporin for intravenous or intramuscular injection. This product has a wider antibacterial spectrum against Gram-negative bacilli than the first-generation cephalosporins. It has good antibacterial activity similar to cefoxitin against Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Citrobacter, Providencia and Enterobacter, but its activity against indole-positive Proteus, Morganella, Providencia and some Klebsiella is lower than that of cefoxitin. It has satisfactory activity against gonococci of influenza bacilli, including beta-lactamase-producing strains. Like other second-generation cephalosporins, Pseudomonas, Serratia and Acinetobacter are resistant to this product. This product is effective against most Gram-positive cocci. Its activity against Staphylococcus aureus is similar to that of cefoxitin and cefuroxime, but lower than that of cefoxitin, cephalothin and cefazolin. 90% of the strains can be inhibited by this product at a concentration of 4.0 to 8.3 mg/L. Most streptococci, including Streptococcus pneumoniae, Streptococcus pyogenes and Group B Streptococcus, are sensitive to this product. Staphylococcus epidermidis is relatively resistant to this product. Streptococcus faecalis, Staphylococcus aureus and methicillin-resistant strains of Staphylococcus epidermidis are all resistant to this product. The activity of this product against anaerobic bacteria has not been well studied, and Bacteroides fragilis is resistant to this product. The minimum bactericidal concentration (MBC) of this product for Staphylococcus aureus, Group B Streptococcus and Escherichia coli is significantly higher than its minimum inhibitory concentration (MIC). This product is very stable to type I beta-lactamase, but can be slowly hydrolyzed by type IIIa, IIIb and V beta-lactamase, while only type IV beta-lactamase is sensitive.

61270-78-8 15
Cefpiramide for injection
The main ingredient of this product is cefpiramide, and its chemical name is: (6R, 7R)-7-[(R)-2-(4-hydroxy-6-methyl-3-pyridinecarbonylamino)-2-(p-hydroxyphenyl)acetylamino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene-2-carboxylic acid.
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Cefpiramide acid

70797-11-4 9
Cefpiramide for injection
The main ingredient of this product is cefpiramide, and its chemical name is: (6R, 7R)-7-[(R)-2-(4-hydroxy-6-methyl-3-pyridinecarbonylamino)-2-(p-hydroxyphenyl)acetylamino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene-2-carboxylic acid.
Name Description Content CAS NO. Registered Holders
Cefpiramide acid

70797-11-4 9
Cefpiramide for injection
The main ingredient of this product is cefpiramide, and its chemical name is: (6R, 7R)-7-[(R)-2-(4-hydroxy-6-methyl-3-pyridinecarbonylamino)-2-(p-hydroxyphenyl)acetylamino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene-2-carboxylic acid.
Name Description Content CAS NO. Registered Holders
Cefpiramide acid

70797-11-4 9
Cefditoren Pivoxil Capsules
The main ingredient of this product is cefditoren pivoxil.
Name Description Content CAS NO. Registered Holders
Cefteram pivoxil

It blocks the synthesis of bacterial cell walls and has strong binding to 3, 1A, 1Bs in penicillin binding protein (PBP). It has antibacterial effects on both Gram-positive and Gram-negative bacteria, especially on Streptococcus, Pneumococcus, Escherichia coli, Klebsiella, Neisseria gonorrhoeae, Haemophilus influenzae, anaerobic bacteria, Streptococcus pyogenes, etc. It also has good antibacterial effects on Serratia, indole-positive Proteus, Enterobacter, Citrobacter, etc. It is effective against strains that produce β-lactamase. No reports of carcinogenicity and teratogenicity have been found.

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It blocks the synthesis of bacterial cell walls and has strong binding to 3, 1A, 1Bs in penicillin binding protein (PBP). It has antibacterial effects on both Gram-positive and Gram-negative bacteria, especially on Streptococcus, Pneumococcus, Escherichia coli, Klebsiella, Neisseria gonorrhoeae, Haemophilus influenzae, anaerobic bacteria, Streptococcus pyogenes, etc. It also has good antibacterial effects on Serratia, indole-positive Proteus, Enterobacter, Citrobacter, etc. It is effective against strains that produce β-lactamase. No reports of carcinogenicity and teratogenicity have been found.

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