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CSPC OUYI Pharmaceutical Co., Ltd.
  • Founded in:

    2001-03-29
  • Country:

    China China
  • Address:

    No. 88, Yangzi Road, Shijiazhuang Economic and Technological Development Zone
  • Tax NO.:

    91130100601289268L
  • Registered Funds:

    298 million yuan
  • Website:

  • Email:

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Cefuroxime for injection
The main ingredient of this product is cefradine, and its chemical name is (6R,7R)-7[(R)-2-amino-2-(1,4-cyclohexenyl)acetylamino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-87-carboxylic acid.
Name Description Content CAS NO. Registered Holders
Cefradine

This product is a first-generation cephalosporin, which has good antibacterial effect on some strains of Gram-positive cocci such as non-penicillinase-producing and penicillinase-producing Staphylococcus aureus, coagulase-negative Staphylococci, group A hemolytic streptococci, Streptococcus pneumoniae and viridans streptococci. Anaerobic Gram-positive bacteria are mostly sensitive to this product, while Bacteroides fragilis is resistant to it. Methicillin-resistant Staphylococci and Enterococci are resistant to this product. The effect of this product on Gram-positive and Gram-negative bacteria is similar to that of cephalexin. This product has a certain effect on gonococci and is also active against enzyme-producing gonococci; its activity against Haemophilus influenzae is poor.

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This product is a first-generation cephalosporin, which has good antibacterial effect on some strains of Gram-positive cocci such as non-penicillinase-producing and penicillinase-producing Staphylococcus aureus, coagulase-negative Staphylococci, group A hemolytic streptococci, Streptococcus pneumoniae and viridans streptococci. Anaerobic Gram-positive bacteria are mostly sensitive to this product, while Bacteroides fragilis is resistant to it. Methicillin-resistant Staphylococci and Enterococci are resistant to this product. The effect of this product on Gram-positive and Gram-negative bacteria is similar to that of cephalexin. This product has a certain effect on gonococci and is also active against enzyme-producing gonococci; its activity against Haemophilus influenzae is poor.

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Compound Rutin Tablets
This product is a compound preparation, its components are: rutin and vitamin C
Name Description Content CAS NO. Registered Holders
Rutin

It is a glycoside of dehydrogenated flavonoids, which often coexists with vitamin C in food. It may participate in the action of oxidoreductase in the body, affect the activity of the thyroid gland, and protect adrenaline from oxidation. In the body, it can enhance the effect of vitamin C and promote its accumulation in the body, maintain vascular elasticity, enhance capillary resistance, reduce its fragility and permeability, and promote its cell proliferation and prevent blood cell aggregation.

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It is a glycoside of dehydrogenated flavonoids, which often coexists with vitamin C in food. It may participate in the action of oxidoreductase in the body, affect the activity of the thyroid gland, and protect adrenaline from oxidation. In the body, it can enhance the effect of vitamin C and promote its accumulation in the body, maintain vascular elasticity, enhance capillary resistance, reduce its fragility and permeability, and promote its cell proliferation and prevent blood cell aggregation.

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Ascorbic Acid

Its main pharmacological effects are to maintain vascular elasticity, enhance capillary resistance, reduce its fragility and permeability, promote cell proliferation and prevent blood cell aggregation.

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Its main pharmacological effects are to maintain vascular elasticity, enhance capillary resistance, reduce its fragility and permeability, promote cell proliferation and prevent blood cell aggregation.

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Compound acetaminophen tablets (Ⅱ)
This product is a compound preparation, each tablet contains 0.25g of acetaminophen, 0.15g of isopropyl antipyrine, and 50mg of anhydrous caffeine. Excipients are: microcrystalline cellulose, hydroxypropyl methylcellulose, formaldehyde casein, corn starch, magnesium stearate, talc, and silicic acid.
Name Description Content CAS NO. Registered Holders
Acetaminophen

Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Propyphenazone

Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Caffeine

Central nervous system stimulant, can enhance the antipyretic and analgesic effects of the first two

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Central nervous system stimulant, can enhance the antipyretic and analgesic effects of the first two

50mg 0
Albendazole tablets
Albendazole Chemical name: [5-(propylthio)-1H-benzimidazol-2-yl] methyl carbamate Molecular formula: C11H16N2O·HCl Molecular weight: 228.72
Name Description Content CAS NO. Registered Holders
Albendazole

This product is a benzimidazole derivative, which is rapidly metabolized into sulfoxide, sulfone alcohol and 2-amine sulfone alcohol in the body. It selectively and irreversibly inhibits the polymerization of the cytoplasmic microtubule system of the parasite's intestinal wall cells, blocks its absorption of various nutrients and glucose, leads to the depletion of endogenous glycogen in the worm, and inhibits the fumarate reductase system, preventing the production of adenosine triphosphate, making it impossible for the worm to survive and reproduce. It can also cause the degeneration of the cytoplasmic microtubules of the worm's intestinal cells, and bind to its microtubule protein, causing intracellular transport blockage, resulting in the accumulation of Golgi endocrine granules, the gradual dissolution of the cytoplasm, and the complete degeneration of the absorbing cells, causing the death of the worm. It has the effect of completely killing hookworm eggs and whipworm eggs and partially killing ascarid eggs. In addition to killing and expelling various nematodes parasitic in animals, it also has a significant killing and expelling effect on tapeworms and cysticerci.

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This product is a benzimidazole derivative, which is rapidly metabolized into sulfoxide, sulfone alcohol and 2-amine sulfone alcohol in the body. It selectively and irreversibly inhibits the polymerization of the cytoplasmic microtubule system of the parasite's intestinal wall cells, blocks its absorption of various nutrients and glucose, leads to the depletion of endogenous glycogen in the worm, and inhibits the fumarate reductase system, preventing the production of adenosine triphosphate, making it impossible for the worm to survive and reproduce. It can also cause the degeneration of the cytoplasmic microtubules of the worm's intestinal cells, and bind to its microtubule protein, causing intracellular transport blockage, resulting in the accumulation of Golgi endocrine granules, the gradual dissolution of the cytoplasm, and the complete degeneration of the absorbing cells, causing the death of the worm. It has the effect of completely killing hookworm eggs and whipworm eggs and partially killing ascarid eggs. In addition to killing and expelling various nematodes parasitic in animals, it also has a significant killing and expelling effect on tapeworms and cysticerci.

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Fosfomycin Sodium for Injection
The main ingredients of this product are: Fosfomycin sodium
Name Description Content CAS NO. Registered Holders
Disodium phosphonomycin

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