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Yichang Humanwell Pharmaceutical Co., Ltd.

  • Founded in:

    2001-08-08
  • Country:

    China China
  • Address:

    No. 19, Dalian Road, Yichang Development Zone, Hubei Province
  • Tax NO.:

    91420500730843405M
  • Registered Funds:

    293,527,036 yuan
  • Website:

  • Email:

Related Drugs
Gliclazide extended-release tablets
Gliclazide, its chemical name is: 1-(3-azabicyclo[3.3.0]oct-3-yl)-3-toluenesulfonylurea.
Name Description Content CAS NO. Registered Holders
Gliclazide

This drug is a hypoglycemic sulfonylurea-oral diabetes treatment drug. Gliclazide lowers blood sugar levels by stimulating pancreatic β cells to secrete insulin. For type 2 diabetes, gliclazide can restore the first-phase insulin secretion peak in response to glucose and increase the second-phase insulin secretion. It can be seen that the insulin secretion response induced or stimulated by glucose after a meal is significantly increased.

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This drug is a hypoglycemic sulfonylurea-oral diabetes treatment drug. Gliclazide lowers blood sugar levels by stimulating pancreatic β cells to secrete insulin. For type 2 diabetes, gliclazide can restore the first-phase insulin secretion peak in response to glucose and increase the second-phase insulin secretion. It can be seen that the insulin secretion response induced or stimulated by glucose after a meal is significantly increased.

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Thiamphenicol Capsules
The main component of this product is thiamphenicol, and its chemical name is [R-(R*,R*)]N-[1-(hydroxymethyl)-2-hydroxy-2-[4-(methylsulfonyl)phenyl]ethyl]2,2,-dichloroacetamide. Its structural formula is: Molecular formula: C12H15Cl2NO5S, molecular weight: 356.23.
Name Description Content CAS NO. Registered Holders
Thiamphenicol

It has a broad spectrum of antimicrobial effects, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has bactericidal effects on Haemophilus influenzae, Streptococcus pneumoniae and Neisseria meningitidis, and only has antibacterial effects 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 completely cross-resistant with chloramphenicol. It has a strong immunosuppressive effect, which is about 6 times stronger than chloramphenicol.

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It has a broad spectrum of antimicrobial effects, including aerobic Gram-negative and Gram-positive bacteria, anaerobes, Rickettsia, spirochetes and Chlamydia. It has bactericidal effects on Haemophilus influenzae, Streptococcus pneumoniae and Neisseria meningitidis, and only has antibacterial effects 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 completely cross-resistant with chloramphenicol. It has a strong immunosuppressive effect, which is about 6 times stronger than chloramphenicol.

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Licorice Zinc Capsules
The main ingredient of this product is a zinc-containing drug that is a combination of an active ingredient extracted from the root of the legume plant licorice and zinc.
Name Description Content CAS NO. Registered Holders
Active ingredients extracted from licorice root

Increase the "glycosamine" content of gastric mucosal cells, improve the defense of gastric mucosa, prolong the life of gastric epithelial cells, and accelerate the healing of ulcers

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Increase the "glycosamine" content of gastric mucosal cells, improve the defense of gastric mucosa, prolong the life of gastric epithelial cells, and accelerate the healing of ulcers

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ZINC

Promote mucosal regeneration and accelerate ulcer healing

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Promote mucosal regeneration and accelerate ulcer healing

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Cimetidine capsules
Cimetidine
Name Description Content CAS NO. Registered Holders
Cimetidine

It can significantly inhibit the day and night basal gastric acid secretion, and can also inhibit the gastric acid secretion induced by food, histamine, pentagastrin, caffeine and insulin.

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It can significantly inhibit the day and night basal gastric acid secretion, and can also inhibit the gastric acid secretion induced by food, histamine, pentagastrin, caffeine and insulin.

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Nitrofurantoin enteric-coated tablets
Molecular weight: C8H6N4O5
Name Description Content CAS NO. Registered Holders
Nitrofurantoin [3H(G)] C8H6N4O5

This product is an antibacterial drug. Escherichia coli is mostly sensitive to this product, and some strains of Enterobacteriaceae such as Enterobacter aerogenes, Enterobacter cloacae, Proteus, and Klebsiella are sensitive to this product. Pseudomonas aeruginosa is usually resistant to this product. This product has antibacterial effects on Gram-positive bacteria such as Enterococcus. The antibacterial activity of this product is not affected by pus and tissue decomposition products. It is more active in acidic urine. The antibacterial mechanism is to interfere with the oxidoreductase system in the bacteria, thereby blocking its metabolic process.

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This product is an antibacterial drug. Escherichia coli is mostly sensitive to this product, and some strains of Enterobacteriaceae such as Enterobacter aerogenes, Enterobacter cloacae, Proteus, and Klebsiella are sensitive to this product. Pseudomonas aeruginosa is usually resistant to this product. This product has antibacterial effects on Gram-positive bacteria such as Enterococcus. The antibacterial activity of this product is not affected by pus and tissue decomposition products. It is more active in acidic urine. The antibacterial mechanism is to interfere with the oxidoreductase system in the bacteria, thereby blocking its metabolic process.

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