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North China Pharmaceutical Company.Ltd
  • Founded in:

    1992-12-20
  • Country:

    China China
  • Address:

    No. 388, Heping East Road, Shijiazhuang City
  • Tax NO.:

    91130100104397700P
  • Registered Funds:

    1,715,730,370 yuan
  • Website:

  • Email:

Related Drugs
Amoxicillin Sodium and Sulbactam Sodium for Injection
Flupenthixol dihydrochloride
Name Description Content CAS NO. Registered Holders
Fupentixol dihydrochloride

It is a thioxanthene derivative with a strong dopamine receptor blocking effect. In addition to blocking D1 and D2 receptors, it can also inhibit D2 autoreceptors and increase the DA concentration between synapses. It has no sedative effect. Its antipsychotic effect is 4 to 8 times stronger than that of Telden. In addition, it also has antidepressant and antianxiety effects.

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It is a thioxanthene derivative with a strong dopamine receptor blocking effect. In addition to blocking D1 and D2 receptors, it can also inhibit D2 autoreceptors and increase the DA concentration between synapses. It has no sedative effect. Its antipsychotic effect is 4 to 8 times stronger than that of Telden. In addition, it also has antidepressant and antianxiety effects.

2413-38-9 0
Amoxicillin Sodium and Sulbactam Sodium for Injection
This product is a compound preparation, and its components are amoxicillin sodium and sulbactam sodium. Chemical name: Amoxicillin sodium: (2S, 5R, 6R)-3,3-dimethyl-6-(R)-(-)-2-amino-2-(4-hydroxyphenyl)-acetylamino 7-oxo-4-thia-1-azabicyclo 3.2.0 heptane-2-carboxylate sodium. Sulbactam sodium: (2S, 5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo 3.2.0 heptane-2-carboxylate sodium-4,4-dioxide.
Name Description Content CAS NO. Registered Holders
Amoxicillin sodium

A bactericidal broad-spectrum antibiotic that can kill a variety of Gram-positive and Gram-negative bacteria. The presence of sulbactam sodium protects it from being destroyed by β-lactamase, so it is still effective against β-lactamase-producing resistant bacteria.

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A bactericidal broad-spectrum antibiotic that can kill a variety of Gram-positive and Gram-negative bacteria. The presence of sulbactam sodium protects it from being destroyed by β-lactamase, so it is still effective against β-lactamase-producing resistant bacteria.

34642-77-8 16
Sulbactam sodium

Irreversible broad-spectrum β-lactamase inhibitors can effectively inhibit β-lactamase produced by drug-resistant bacteria and enhance the effect of amoxicillin against drug-resistant bacteria.

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Irreversible broad-spectrum β-lactamase inhibitors can effectively inhibit β-lactamase produced by drug-resistant bacteria and enhance the effect of amoxicillin against drug-resistant bacteria.

69388-84-7 30
Amoxicillin Sodium and Sulbactam Sodium for Injection
Amoxicillin sodium: sodium (2S, 5R, 6R)-3,3-dimethyl-6-[(R)-(-)-2-(4-hydroxyphenyl)ethylamino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Sulbactam sodium: sodium (2S, 5R)-3,3-dimethyl-7-oxido-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4,4-dioxide.
Name Description Content CAS NO. Registered Holders
Amoxicillin sodium

A bactericidal broad-spectrum antibiotic that can kill a variety of Gram-positive and Gram-negative bacteria. When used in combination with sulbactam sodium, it can protect against the destruction of β-lactamase and has a special effect on resistant bacteria that produce β-lactamase.

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A bactericidal broad-spectrum antibiotic that can kill a variety of Gram-positive and Gram-negative bacteria. When used in combination with sulbactam sodium, it can protect against the destruction of β-lactamase and has a special effect on resistant bacteria that produce β-lactamase.

34642-77-8 16
Sulbactam sodium

Irreversible broad-spectrum β-lactamase inhibitor that protects amoxicillin from destruction by β-lactamase and enhances its antibacterial activity against drug-resistant bacteria.

More

Irreversible broad-spectrum β-lactamase inhibitor that protects amoxicillin from destruction by β-lactamase and enhances its antibacterial activity against drug-resistant bacteria.

69388-84-7 30
Amoxicillin Sodium and Sulbactam Sodium for Injection
Amoxicillin sodium: sodium (2S, 5R, 6R)-3,3-dimethyl-6-[(R)-(-)-2-(4-hydroxyphenyl)ethylamino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Sulbactam sodium: sodium (2S, 5R)-3,3-dimethyl-7-oxido-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4,4-dioxide.
Name Description Content CAS NO. Registered Holders
Amoxicillin sodium

It is a bactericidal broad-spectrum antibiotic. When used in combination with sulbactam sodium, it can be protected from destruction by β-lactamase and has antibacterial effects on a variety of Gram-positive and Gram-negative bacteria.

More

It is a bactericidal broad-spectrum antibiotic. When used in combination with sulbactam sodium, it can be protected from destruction by β-lactamase and has antibacterial effects on a variety of Gram-positive and Gram-negative bacteria.

34642-77-8 16
Sulbactam sodium

Irreversible broad-spectrum β-lactamase inhibitor that protects amoxicillin from destruction by β-lactamases and enhances its effectiveness against β-lactamase-producing resistant bacteria.

More

Irreversible broad-spectrum β-lactamase inhibitor that protects amoxicillin from destruction by β-lactamases and enhances its effectiveness against β-lactamase-producing resistant bacteria.

69388-84-7 30
Ranitidine Hydrochloride Injection
The main ingredient of this product is: Ranitidine hydrochloride. Its chemical name is: Nprime;-methyl-N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]-methyl]thio]ethyl]-2-nitro-1,1-ethylenediamine hydrochloride. Structural formula: (see Ranitidine hydrochloride capsules) Molecular formula: C13H22N4O3SHCl Molecular weight: 350.87
Name Description Content CAS NO. Registered Holders
Ranitidine Hydrochloride

H2 receptor antagonists can significantly inhibit the basal and nocturnal gastric acid secretion in normal people and ulcer patients, as well as the gastric acid secretion caused by pentagastrin, histamine and meals. They have a certain inhibitory effect on the secretion of pepsinogen, and have a protective effect on experimental gastric mucosal damage and acute ulcers. They have no effect on the secretion of gastrin and sex hormones.

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H2 receptor antagonists can significantly inhibit the basal and nocturnal gastric acid secretion in normal people and ulcer patients, as well as the gastric acid secretion caused by pentagastrin, histamine and meals. They have a certain inhibitory effect on the secretion of pepsinogen, and have a protective effect on experimental gastric mucosal damage and acute ulcers. They have no effect on the secretion of gastrin and sex hormones.

66357-59-3 48
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