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Shanxi Sanjin Pharmaceutical Co., Ltd.
  • Founded in:

    1999-01-28
  • Country:

    China China
  • Address:

    No. 1001, Middle Section of Tongge Street, Xiaohe Industrial Park, Shanxi Transformation and Comprehensive Reform Demonstration Zone
  • Tax NO.:

    91140100713652658Q
  • Registered Funds:

    66 million yuan
  • Website:

  • Email:

Related Drugs
Tetracycline Hydrochloride Capsules
The main ingredient of this product is tetracycline hydrochloride. Its chemical name is 6-methyl-4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-2-naphthacenecarboxamide hydrochloride.
Name Description Content CAS NO. Registered Holders
Tetracycline hydrochloride

This product is a broad-spectrum antibacterial agent, with bactericidal effect at high concentrations. It has antibacterial effects on Streptococcus pneumoniae, hemolytic Streptococcus, Streptococcus viridans and some Staphylococci, Clostridium perfringens, Bacillus anthracis, Bacillus plague, Corynebacterium diphtheriae, Corynebacterium tetani, Brucella, Haemophilus influenzae, Campylobacter, Vibrio cholerae, etc. It also has inhibitory effects on Rickettsia, Mycoplasma, Chlamydia, Spirochete, and some protozoa. This product has better effects on Gram-positive bacteria than Gram-negative bacteria, but Enterococcus is resistant to it. In addition, it is also sensitive to Actinomyces, Bacillus anthracis, Listeria monocytogenes, Clostridium, Nocardia, etc. The mechanism of action is that the drug can specifically bind to the A position of the 30S subunit of the bacterial ribosome, preventing the connection of aminoacyl-tRNA at this position, thereby inhibiting the growth of the peptide chain and affecting the synthesis of bacterial proteins.

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This product is a broad-spectrum antibacterial agent, with bactericidal effect at high concentrations. It has antibacterial effects on Streptococcus pneumoniae, hemolytic Streptococcus, Streptococcus viridans and some Staphylococci, Clostridium perfringens, Bacillus anthracis, Bacillus plague, Corynebacterium diphtheriae, Corynebacterium tetani, Brucella, Haemophilus influenzae, Campylobacter, Vibrio cholerae, etc. It also has inhibitory effects on Rickettsia, Mycoplasma, Chlamydia, Spirochete, and some protozoa. This product has better effects on Gram-positive bacteria than Gram-negative bacteria, but Enterococcus is resistant to it. In addition, it is also sensitive to Actinomyces, Bacillus anthracis, Listeria monocytogenes, Clostridium, Nocardia, etc. The mechanism of action is that the drug can specifically bind to the A position of the 30S subunit of the bacterial ribosome, preventing the connection of aminoacyl-tRNA at this position, thereby inhibiting the growth of the peptide chain and affecting the synthesis of bacterial proteins.

64-75-5 30
Wei Yan Kang Capsule
White peony root, licorice root, cinnamon twig, galangal, coptis root, bupleurum root. No auxiliary materials.
Name Description Content CAS NO. Registered Holders
PAEONIAE RADIX ALBA

0
DGL

0
Cmnamomi Mmulus

0
Alpiniae Officinarum Rhizoma

0
COPTIDISRHIZOMA

0
Bupleurum

0
Metformin Glibenclamide Capsules (Ⅰ)
This product is a compound preparation, and its components are: each tablet contains 1.25 mg of glibenclamide and 250 mg of metformin hydrochloride.
Name Description Content CAS NO. Registered Holders
Glibenclamide

Mainly stimulates pancreatic β cells to secrete insulin to produce blood sugar lowering effect

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Mainly stimulates pancreatic β cells to secrete insulin to produce blood sugar lowering effect

1.25mg 10238-21-8 28
1,1-DIMETHYLBIGUANIDE HYDROCHLORIDE

It can reduce the production of liver glycogen, reduce intestinal absorption of sugar, and improve insulin sensitivity by increasing peripheral sugar uptake and utilization

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It can reduce the production of liver glycogen, reduce intestinal absorption of sugar, and improve insulin sensitivity by increasing peripheral sugar uptake and utilization

250mg 15537-72-1 55
Compound sulfamethoxazole granules for children
Compound preparation. Each bag contains 100 mg of sulfamethoxazole and 20 mg of trimethoprim, and the auxiliary material is white sugar.
Name Description Content CAS NO. Registered Holders
Sulfamethoxazole

This product is a sulfonamide antibiotic. When used in combination with trimethoprim, it can double block the bacterial folic acid metabolism and enhance the synergistic antibacterial effect, especially the antibacterial effect on Escherichia coli, Haemophilus influenzae, and Staphylococcus aureus is significantly enhanced compared with a single drug.

More

This product is a sulfonamide antibiotic. When used in combination with trimethoprim, it can double block the bacterial folic acid metabolism and enhance the synergistic antibacterial effect, especially the antibacterial effect on Escherichia coli, Haemophilus influenzae, and Staphylococcus aureus is significantly enhanced compared with a single drug.

100mg 723-46-6 33
Trimethoprim

This product is a sulfonamide antibiotic. When used in combination with sulfamethoxazole, it can double block the bacterial folic acid metabolism, enhance the synergistic antibacterial effect, and reduce drug-resistant strains.

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This product is a sulfonamide antibiotic. When used in combination with sulfamethoxazole, it can double block the bacterial folic acid metabolism, enhance the synergistic antibacterial effect, and reduce drug-resistant strains.

20mg 738-70-5 44
Ranitidine Hydrochloride Capsules
Ranitidine hydrochloride, its chemical name is: N'-methyl-N-[2-[[[5-[(dimethylamino)methyl]-2-furyl]-methyl]thio]ethyl]-2-nitro-1,1-ethylenediamine hydrochloride.
Name Description Content CAS NO. Registered Holders
Ranitidine Hydrochloride

It has the effect of competitively blocking the binding of histamine to H2 receptors and inhibiting the effect of gastric acid. Its molarity is 5 to 12 times that of cimetidine, making it a potent H2 receptor blocker.

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It has the effect of competitively blocking the binding of histamine to H2 receptors and inhibiting the effect of gastric acid. Its molarity is 5 to 12 times that of cimetidine, making it a potent H2 receptor blocker.

66357-59-3 49
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