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Changchun Haiwang Biological Pharmaceutical Co., Ltd.
  • Founded in:

    1995-01-25
  • Country:

    China China
  • Address:

    No. 833, Huoju Road, Qianjin Street, High-tech Development Zone, Changchun City, Jilin Province;
  • Tax NO.:

    91220101243880532N
  • Registered Funds:

    20 million yuan
  • Website:

  • Email:

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FRITILLARIAE USSURIENSIS BULBUS

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polygala

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Ephedrine hydrochloride

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Sucrose

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Children's Guangpu Antidiarrhea Oral Liquid
Patchouli, Atractylodes, Poria, Alisma, Magnolia officinalis (processed with ginger), Plantain, Tangerine peel, and Liushenqu (fried).
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POGOSTEMONIS HERBA

Inhibits gastric emptying and propulsive motility of the small intestine in mice, fights rhubarb-induced diarrhea in mice and rotavirus-induced diarrhea in tree shrews, and promotes the phagocytic function of peritoneal macrophages and the formation of anti-sheep red blood cell antibodies in "spleen deficiency" mice

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ATRACTYLODIS RHIZOMA

Inhibits gastric emptying and propulsive motility of the small intestine in mice, fights rhubarb-induced diarrhea in mice and rotavirus-induced diarrhea in tree shrews, and promotes the phagocytic function of peritoneal macrophages and the formation of anti-sheep red blood cell antibodies in "spleen deficiency" mice

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Poria

Inhibits gastric emptying and propulsive motility of the small intestine in mice, fights rhubarb-induced diarrhea in mice and rotavirus-induced diarrhea in tree shrews, and promotes the phagocytic function of peritoneal macrophages and the formation of anti-sheep red blood cell antibodies in "spleen deficiency" mice

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ALISMATIS RHIZOMA

Inhibits gastric emptying and propulsive motility of the small intestine in mice, fights rhubarb-induced diarrhea in mice and rotavirus-induced diarrhea in tree shrews, and promotes the phagocytic function of peritoneal macrophages and the formation of anti-sheep red blood cell antibodies in "spleen deficiency" mice

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Magnolia officinalis (prepared with ginger)

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HERBA PLANTAGINIS

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Citri reticulatae pericarpium

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Six-spirited Sauce (fried)

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Moxonidine Hydrochloride Tablets
The main ingredient of this product is moxonidine hydrochloride. 4-Chloro-N-(4,5-dihydro-1-hydro-imidazolyl-2)-6-methoxy-2-methyl-5-aminopyrimidine hydrochloride monohydrate
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Moxonidine hydrochloride

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Moxonidine is a new type of central antihypertensive drug. It is a selective agonist with high affinity for imidazoline I1 receptors. The antihypertensive effect of this product has no obvious relationship with the binding of alpha 2 adrenergic receptors. Pharmacological experiments on mice show that this product can reduce the number of spontaneous activities, promote sleep in mice in synergy with pentobarbital, and inhibit central nervous system activity; it slows down the heart rate while lowering blood pressure, but has no obvious effect on the ECG and respiratory rate and depth.

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Oxaprozin Tablets
The main ingredient of this product is oxaprozin.
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Oxaprozin

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Fluconazole for injection
Ingredients: Fluconazole. Chemical name: alpha;-(2,4-difluorophenyl)-alpha;-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-triazol-1-ylethanol.
Name Description Content CAS NO. Registered Holders
Fluconazole

Fluconazole is a triazole broad-spectrum antifungal drug that inhibits the reproduction and growth of fungi by highly selectively inhibiting the C-14-alpha;-demethylation of fungal cytochrome P-450 sterols, causing the accumulation of 14-alpha;-methyl sterols in fungi. In vitro tests have shown that this product has antibacterial activity against Cryptococcus neoformans and Candida species. Oral and intravenous injection of fluconazole in animals is effective in the following animal fungal infection models: Candida infection (including systemic candidiasis in immunodeficient animals); Cryptococcus neoformans infection (including intracranial infection); Microsporum and Trichophyton infection, etc. Fluconazole is also effective against Blastomyces dermatitidis infection and Coccidioides immitis infection (including intracranial infection); and is also effective against infections caused by Histoplasma capsulatum in normal animals and immunosuppressed animals.

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Fluconazole is a triazole broad-spectrum antifungal drug that inhibits the reproduction and growth of fungi by highly selectively inhibiting the C-14-alpha;-demethylation of fungal cytochrome P-450 sterols, causing the accumulation of 14-alpha;-methyl sterols in fungi. In vitro tests have shown that this product has antibacterial activity against Cryptococcus neoformans and Candida species. Oral and intravenous injection of fluconazole in animals is effective in the following animal fungal infection models: Candida infection (including systemic candidiasis in immunodeficient animals); Cryptococcus neoformans infection (including intracranial infection); Microsporum and Trichophyton infection, etc. Fluconazole is also effective against Blastomyces dermatitidis infection and Coccidioides immitis infection (including intracranial infection); and is also effective against infections caused by Histoplasma capsulatum in normal animals and immunosuppressed animals.

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