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Suzhou Pharmaceutical Factory

  • Founded in:

    2006-02-14
  • Country:

    China China
  • Address:

    No. 2-1, Dongwu South Road, Wuzhong District, Suzhou City
  • Tax NO.:

    91320506138170408U
  • Registered Funds:

    -
  • Website:

  • Email:

Related Drugs
Sisomicin Sulfate Injection
Sisomicin sulfate.
Name Description Content CAS NO. Registered Holders
Sisomycin Sulfate

53179-09-2 3
Sisomicin Sulfate Injection
Sisomicin sulfate.
Name Description Content CAS NO. Registered Holders
Sisomycin Sulfate

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53179-09-2 3
Pantoprazole sodium
Name Description Content CAS NO. Registered Holders
Pantoprazole Sodium

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138786-67-1 58
Thiamphenicol Enteric-coated Tablets
The main ingredient of this product is thiamphenicol. Its chemical name is [R-(R*,R*)]N-{1-(hydroxymethyl)-2-hydroxy-2-[4-(methylsulfonyl)phenyl]ethyl}2,2-dichloroacetamide. Molecular formula: C12H15Cl2NO5S Molecular weight: 356.23
Name Description Content CAS NO. Registered Holders
Thiamphenicol

It has a broad-spectrum antimicrobial effect, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has a bactericidal effect on Haemophilus influenzae, Streptococcus pneumoniae and Neisseria meningitidis, and only has an antibacterial effect on anaerobic bacteria such as Staphylococcus aureus, Streptococcus pyogenes, Streptococcus viridans, Group B hemolytic Streptococcus, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Salmonella typhi, Salmonella paratyphi, Shigella, Bacteroides fragilis, etc. It is usually resistant to Pseudomonas aeruginosa, Acinetobacter, Enterobacter, Serratia marcescens, indole-positive Proteus, methicillin-resistant Staphylococcus and Enterococcus. This product is an antibacterial agent that reversibly binds to the 50S subunit of the bacterial ribosome, inhibits protein synthesis, and is completely cross-resistant with chloramphenicol. It has a strong immunosuppressive effect, about 6 times stronger than chloramphenicol.

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It has a broad-spectrum antimicrobial effect, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has a bactericidal effect on Haemophilus influenzae, Streptococcus pneumoniae and Neisseria meningitidis, and only has an antibacterial effect on anaerobic bacteria such as Staphylococcus aureus, Streptococcus pyogenes, Streptococcus viridans, Group B hemolytic Streptococcus, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Salmonella typhi, Salmonella paratyphi, Shigella, Bacteroides fragilis, etc. It is usually resistant to Pseudomonas aeruginosa, Acinetobacter, Enterobacter, Serratia marcescens, indole-positive Proteus, methicillin-resistant Staphylococcus and Enterococcus. This product is an antibacterial agent that reversibly binds to the 50S subunit of the bacterial ribosome, inhibits protein synthesis, and is completely cross-resistant with chloramphenicol. It has a strong immunosuppressive effect, about 6 times stronger than chloramphenicol.

15318-45-3 4
Coenzyme Q10 capsules
Coenzyme Q10 chemical name: 2-(3,7,11,15,19,23,27,31,35,39-decylmethyl-2,6,10,14,18,22,26,30,34,38-tetradecenyl)-5,6-dimethoxy-3-methyl-p-benzoquinone. Molecular formula: C59H90O4 Molecular weight: 863.36
Name Description Content CAS NO. Registered Holders
Coenzyme Q10

In acute toxicity experiments, the LD50 in mice and rats was greater than 4000 mg/Kg. In subacute toxicity experiments, Wistar male and female rats were given 40 mg, 200 mg and 1000 mg/Kg per day for 5 weeks, and male and female rabbits were given 6 mg, 60 mg and 600 mg/Kg per day for 23 consecutive days. There were no special changes in the blood, urine and morphological observations of the test animals. In chronic toxicity experiments, Wistar male and female rats were given 6 mg, 60 mg and 600 mg/Kg per day for 26 consecutive weeks. There were no special changes in the general state, blood and urine examinations, and morphological observations of the test animals.

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In acute toxicity experiments, the LD50 in mice and rats was greater than 4000 mg/Kg. In subacute toxicity experiments, Wistar male and female rats were given 40 mg, 200 mg and 1000 mg/Kg per day for 5 weeks, and male and female rabbits were given 6 mg, 60 mg and 600 mg/Kg per day for 23 consecutive days. There were no special changes in the blood, urine and morphological observations of the test animals. In chronic toxicity experiments, Wistar male and female rats were given 6 mg, 60 mg and 600 mg/Kg per day for 26 consecutive weeks. There were no special changes in the general state, blood and urine examinations, and morphological observations of the test animals.

303-98-0 14
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