On ECHEMI
Home > Drugs > Shanxi Zhendong Anxin Biopharmaceutical Co., Ltd.
Shanxi Zhendong Anxin Biopharmaceutical Co., Ltd.
  • Founded in:

    1992-06-12
  • Country:

    China China
  • Address:

    No. 908, Jicheng Road, Huitong Industrial Park, Jinzhong Development Zone, Shanxi Demonstration Zone, Jinzhong City, Shanxi Province
  • Tax NO.:

    91140700602052641X
  • Registered Funds:

    170 million yuan
  • Website:

  • Email:

Related Drugs
Flunarizine Hydrochloride Capsules
The main component of this product is flunarizine hydrochloride. The chemical name is: (E)-1-[bis(4-fluorophenyl)methyl]-4-2(2-propenyl-3-phenyl)-piperazine dihydrochloride. Its structural formula is: Molecular formula: C26H26F2N2·2HCl Molecular weight: 477.42
Name Description Content CAS NO. Registered Holders
Flunarizine dihydrochloride

This product is a calcium channel blocker that can prevent cell damage caused by pathological intracellular calcium overload due to ischemia and other causes; it has the effects of relieving vasospasm, vestibular inhibition, anti-epileptic effect, myocardial protection, improving renal function and anti-histamine.

More

This product is a calcium channel blocker that can prevent cell damage caused by pathological intracellular calcium overload due to ischemia and other causes; it has the effects of relieving vasospasm, vestibular inhibition, anti-epileptic effect, myocardial protection, improving renal function and anti-histamine.

30484-77-6 25
Bifonazole gel
Each gram of this product contains 10 mg of the main ingredient bifonazole, whose chemical name is: () 1-(-biphenyl-4-ylbenzyl)-1H-imidazole. Its chemical structure is: Molecular formula: C22H18N2, molecular weight: 310.40.
Name Description Content CAS NO. Registered Holders
Bifonazole

This product is a broad-spectrum antifungal drug. Its mechanism of action is to inhibit the synthesis of cell membranes. It has antibacterial effects on dermatophytes and Candida.

More

This product is a broad-spectrum antifungal drug. Its mechanism of action is to inhibit the synthesis of cell membranes. It has antibacterial effects on dermatophytes and Candida.

10mg 60628-96-8 11
Hydroxyurea tablets
The chemical name of this product is: Hydroxyurea. Its structural formula is: Molecular formula: CH4N2O2 Molecular weight: 76.06
Name Description Content CAS NO. Registered Holders
Hydroxyurea

It is a nucleoside diphosphate reductase inhibitor that can prevent nucleotides from being reduced to deoxynucleotides, interfere with the biosynthesis of purine and pyrimidine bases, selectively inhibit DNA synthesis, and have no blocking effect on RNA and protein synthesis. It is a cycle-specific drug, and is sensitive to S-phase cells.

More

It is a nucleoside diphosphate reductase inhibitor that can prevent nucleotides from being reduced to deoxynucleotides, interfere with the biosynthesis of purine and pyrimidine bases, selectively inhibit DNA synthesis, and have no blocking effect on RNA and protein synthesis. It is a cycle-specific drug, and is sensitive to S-phase cells.

127-07-1 14
Chloramphenicol Injection
The main ingredient of this product is chloramphenicol, and its chemical name is D-threo-(-)-N-[α-(hydroxymethyl)-β-hydroxy-p-nitrophenylethyl]-2,2-dichloroacetamide.
Name Description Content CAS NO. Registered Holders
Chloramphenicol

It has a broad-spectrum antimicrobial effect in vitro, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has a bactericidal effect on influenza bacilli, Streptococcus pneumoniae and Neisseria meningitidis; it only has an antibacterial effect on anaerobic bacteria such as Staphylococcus aureus, Streptococcus pyogenes, Streptococcus viridans, group B hemolytic streptococci, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Salmonella typhi, Salmonella paratyphi, Shigella, Bacteroides fragilis, etc. Pseudomonas aeruginosa, Acinetobacter, Enterobacter, Serratia marcescens, indole-positive Proteus, methicillin-resistant Staphylococcus and Enterococcus are usually resistant to chloramphenicol. Chloramphenicol is fat-soluble, enters bacterial cells by diffusion, and reversibly binds to the 50S subunit of the bacterial ribosome, inhibiting the action of transpeptidase and preventing protein synthesis.

More

It has a broad-spectrum antimicrobial effect in vitro, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has a bactericidal effect on influenza bacilli, Streptococcus pneumoniae and Neisseria meningitidis; it only has an antibacterial effect on anaerobic bacteria such as Staphylococcus aureus, Streptococcus pyogenes, Streptococcus viridans, group B hemolytic streptococci, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Salmonella typhi, Salmonella paratyphi, Shigella, Bacteroides fragilis, etc. Pseudomonas aeruginosa, Acinetobacter, Enterobacter, Serratia marcescens, indole-positive Proteus, methicillin-resistant Staphylococcus and Enterococcus are usually resistant to chloramphenicol. Chloramphenicol is fat-soluble, enters bacterial cells by diffusion, and reversibly binds to the 50S subunit of the bacterial ribosome, inhibiting the action of transpeptidase and preventing protein synthesis.

56-75-7 14
Guaifenesin Tablets
The main ingredient of this product is guaifenesin.
Name Description Content CAS NO. Registered Holders
Guaifenesin

Guaifenesin is an expectorant that can stimulate the gastric mucosa reflex to increase the secretion of bronchial mucosal glands, reduce the viscosity of sputum, and make sticky sputum easier to cough up.

More

Guaifenesin is an expectorant that can stimulate the gastric mucosa reflex to increase the secretion of bronchial mucosal glands, reduce the viscosity of sputum, and make sticky sputum easier to cough up.

93-14-1 30
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.