On ECHEMI
Home > Drugs > Qilu Pharmaceutical Co., Ltd.

Qilu Pharmaceutical Co., Ltd.

  • Founded in:

    1992-08-21
  • Country:

    China China
  • Address:

    No. 317, Xinluo Street, High-tech Zone, Jinan City, Shandong Province
  • Tax NO.:

    91370000614073351Q
  • Registered Funds:

    600 million yuan
  • Website:

  • Email:

Related Drugs
Mezlocillin Sodium for Injection
The main ingredient of this product is mezlocillin sodium, and its chemical name is (2S, 5R, 6R)-3,3-dimethyl-6-[(R)-2[3-(methylsulfonyl)-2-oxo-1-imidazolidinecarboxamido]-2-phenylacetylamino]-7-oxo-4-thia-1-azabicyclo[3.2.0]-heptane-2-carboxylic acid sodium salt.
Name Description Content CAS NO. Registered Holders
Mezlocillin sodium

This product is a semi-synthetic penicillin antibiotic. It has antibacterial effects on Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Proteus, Enterobacter, Citrobacter, Serratia, Acinetobacter, and Gram-positive cocci sensitive to penicillin. It has a bactericidal effect in large doses. Its antibacterial activity against Escherichia coli, Enterobacter, Klebsiella pneumoniae, Citrobacter, Serratia, and Acinetobacter is stronger than carbenicillin and ampicillin; its antibacterial activity against indole-positive Proteus and Pseudomonas aeruginosa is stronger than carbenicillin and sulbenicillin; its antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus is similar to that of carbenicillin, and its antibacterial activity against Streptococcus faecalis is superior to that of carbenicillin and sulbenicillin. It has good antibacterial effect on most anaerobic bacteria such as Bacteroides fragilis. In vitro tests of this product show that it is unstable to (lactamase produced by bacteria. This product has a significant synergistic effect when used in combination with aminoglycoside antibiotics such as gentamicin and kanamycin.

More

This product is a semi-synthetic penicillin antibiotic. It has antibacterial effects on Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Proteus, Enterobacter, Citrobacter, Serratia, Acinetobacter, and Gram-positive cocci sensitive to penicillin. It has a bactericidal effect in large doses. Its antibacterial activity against Escherichia coli, Enterobacter, Klebsiella pneumoniae, Citrobacter, Serratia, and Acinetobacter is stronger than carbenicillin and ampicillin; its antibacterial activity against indole-positive Proteus and Pseudomonas aeruginosa is stronger than carbenicillin and sulbenicillin; its antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus is similar to that of carbenicillin, and its antibacterial activity against Streptococcus faecalis is superior to that of carbenicillin and sulbenicillin. It has good antibacterial effect on most anaerobic bacteria such as Bacteroides fragilis. In vitro tests of this product show that it is unstable to (lactamase produced by bacteria. This product has a significant synergistic effect when used in combination with aminoglycoside antibiotics such as gentamicin and kanamycin.

59798-30-0 13
Mezlocillin Sodium for Injection
The main ingredient of this product is mezlocillin sodium, and its chemical name is (2S, 5R, 6R)-3,3-dimethyl-6-[(R)-2[3-(methylsulfonyl)-2-oxo-1-imidazolidinecarboxamido]-2-phenylacetylamino]-7-oxo-4-thia-1-azabicyclo[3.2.0]-heptane-2-carboxylic acid sodium salt.
Name Description Content CAS NO. Registered Holders
Mezlocillin sodium

This product is a semi-synthetic penicillin antibiotic. It has antibacterial effects on Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Proteus, Enterobacter, Citrobacter, Serratia, Acinetobacter, and Gram-positive cocci sensitive to penicillin. It has a bactericidal effect in large doses. Its antibacterial activity against Escherichia coli, Enterobacter, Klebsiella pneumoniae, Citrobacter, Serratia, and Acinetobacter is stronger than carbenicillin and ampicillin; its antibacterial activity against indole-positive Proteus and Pseudomonas aeruginosa is stronger than carbenicillin and sulbenicillin; its antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus is similar to that of carbenicillin, and its antibacterial activity against Streptococcus faecalis is superior to that of carbenicillin and sulbenicillin. It has good antibacterial effect on most anaerobic bacteria such as Bacteroides fragilis. In vitro tests of this product show that it is unstable to (lactamase produced by bacteria. This product has a significant synergistic effect when used in combination with aminoglycoside antibiotics such as gentamicin and kanamycin.

More

This product is a semi-synthetic penicillin antibiotic. It has antibacterial effects on Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Proteus, Enterobacter, Citrobacter, Serratia, Acinetobacter, and Gram-positive cocci sensitive to penicillin. It has a bactericidal effect in large doses. Its antibacterial activity against Escherichia coli, Enterobacter, Klebsiella pneumoniae, Citrobacter, Serratia, and Acinetobacter is stronger than carbenicillin and ampicillin; its antibacterial activity against indole-positive Proteus and Pseudomonas aeruginosa is stronger than carbenicillin and sulbenicillin; its antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus is similar to that of carbenicillin, and its antibacterial activity against Streptococcus faecalis is superior to that of carbenicillin and sulbenicillin. It has good antibacterial effect on most anaerobic bacteria such as Bacteroides fragilis. In vitro tests of this product show that it is unstable to (lactamase produced by bacteria. This product has a significant synergistic effect when used in combination with aminoglycoside antibiotics such as gentamicin and kanamycin.

59798-30-0 13
Calcium folinate
Name Description Content CAS NO. Registered Holders
Calcium levofolinate

Extract from the above information

More

Extract from the above information

80433-71-2 14
Bromfenac sodium eye drops
The main ingredient of this product is bromfenac sodium. Chemical name: 2-amino-3-(4-bromobenzoyl)phenylacetic acid sodium sesquihydrate. Chemical structure: Molecular formula: C15H11BrNNaO3·11/2H2O Molecular weight: 383.17
Name Description Content CAS NO. Registered Holders
Bromfenac Sodium

It has an anti-inflammatory effect on experimental conjunctival edema in rats; it has an almost complete inhibitory effect on the increase in aqueous humor protein concentration after anterior chamber puncture or laser irradiation in rabbits; it has an inhibitory effect on the production of inflammatory mediators of the prostaglandin system through cyclooxygenase (invitro).

More

It has an anti-inflammatory effect on experimental conjunctival edema in rats; it has an almost complete inhibitory effect on the increase in aqueous humor protein concentration after anterior chamber puncture or laser irradiation in rabbits; it has an inhibitory effect on the production of inflammatory mediators of the prostaglandin system through cyclooxygenase (invitro).

120638-55-3 18
Cisplatin
Name Description Content CAS NO. Registered Holders
Cisplatin

It is not possible to clearly extract a specific description of the pharmacological action from the above information

More

It is not possible to clearly extract a specific description of the pharmacological action from the above information

15663-27-1 31
Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.