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Hainan Pharmaceutical FACTORY Co., Ltd.

  • Founded in:

    2001-07-09
  • Country:

    China China
  • Address:

    Hebei West Road, Wuzhishan City, Hainan Province
  • Tax NO.:

    91469001730040768G
  • Registered Funds:

    12.8 million yuan
  • Website:

  • Email:

Related Drugs
Lincomycin Hydrochloride Injection
The main ingredient is lincomycin hydrochloride, and its chemical name is 6-(1-methyl-trans-4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-6,8-dideoxy-D-erythro-alpha;-D-galacto-octinopyranoside hydrochloride hydrate. Its structural formula is: Molecular formula: C18H34N2O6SHClH2O Molecular weight: 461.02
Name Description Content CAS NO. Registered Holders
Lincomycin hydrochloride

It has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, beta-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium diphtheriae, and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae, and Haemophilus influenzae, as well as fungi. There is no cross-resistance between this product and penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. This product acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria.

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It has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, beta-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium diphtheriae, and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae, and Haemophilus influenzae, as well as fungi. There is no cross-resistance between this product and penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. This product acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria.

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Isatis root injection
Isatis root.
Name Description Content CAS NO. Registered Holders
Isatidis Radix

0
Cimetidine injection
The main ingredient of this product is cimetidine, and its chemical name is: N-methyl-N-[2[[(5-methyl-1H-imidazol-4-yl)methyl]thio]ethyl]-N-cyanoguanidine.
Name Description Content CAS NO. Registered Holders
Cimetidine

This product is a histamine H2-receptor antagonist, which blocks the effect of histamine on the H2-receptor of parietal cells through a competitive inhibition mechanism. It inhibits basal gastric acid secretion during the day and at night, and inhibits gastric acid secretion caused by food, histamine, pentagastrin, caffeine and insulin. In addition, cimetidine is a powerful inhibitor of irritant gastric acid secretion. When the blood drug concentration reaches a certain level, it can significantly inhibit gastric acid secretion, while reducing gastric juice secretion and pepsin activity.

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This product is a histamine H2-receptor antagonist, which blocks the effect of histamine on the H2-receptor of parietal cells through a competitive inhibition mechanism. It inhibits basal gastric acid secretion during the day and at night, and inhibits gastric acid secretion caused by food, histamine, pentagastrin, caffeine and insulin. In addition, cimetidine is a powerful inhibitor of irritant gastric acid secretion. When the blood drug concentration reaches a certain level, it can significantly inhibit gastric acid secretion, while reducing gastric juice secretion and pepsin activity.

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Fenbufen Tablets
The main ingredient of this product is fenbufen (C16H14O3), whose chemical name is 3-(4-biphenylcarbonyl) propionic acid. Its structural formula is: Molecular formula: C16H14O3 Molecular weight: 254.28
Name Description Content CAS NO. Registered Holders
Fenbufen

This product is a long-acting non-steroidal anti-inflammatory drug. It can inhibit the activity of cyclooxygenase and reduce the synthesis of prostaglandins. Animal experiments show that the anti-inflammatory and analgesic effects of this product are weaker than indomethacin, but stronger than aspirin.

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This product is a long-acting non-steroidal anti-inflammatory drug. It can inhibit the activity of cyclooxygenase and reduce the synthesis of prostaglandins. Animal experiments show that the anti-inflammatory and analgesic effects of this product are weaker than indomethacin, but stronger than aspirin.

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Ammonium iodide lozenges
Name Description Content CAS NO. Registered Holders
Ammonium iodide

No specific pharmacological effects mentioned

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No specific pharmacological effects mentioned

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