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Shanghai BAOLONG Pharmaceutical Co., Ltd.

  • Founded in:

    1993-09-02
  • Country:

    China China
  • Address:

    No. 358, Tianchen Road, Qingpu District, Shanghai
  • Tax NO.:

    91310118134354787F
  • Registered Funds:

    100 million yuan
  • Website:

  • Email:

Related Drugs
Ranitidine hydrochloride syrup
Name Description Content CAS NO. Registered Holders
Ranitidine Hydrochloride

Inhibit gastric acid secretion

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Inhibit gastric acid secretion

66357-59-3 48
Inositol Nicotinate Ointment
Contains inositol nicotinate. Molecular formula: C42H30N6O12 Molecular weight: 810.72
Name Description Content CAS NO. Registered Holders
Inositol nicotinate

This product can selectively dilate blood vessels in diseased areas and areas sensitive to cold stimulation, relieve vascular spasms, and improve peripheral blood circulation.

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This product can selectively dilate blood vessels in diseased areas and areas sensitive to cold stimulation, relieve vascular spasms, and improve peripheral blood circulation.

6556-11-2 9
Thymosin enteric-coated capsules
This product is a biologically active polypeptide substance extracted from bovine thymus with a molecular weight of less than 10,000 Daltons.
Name Description Content CAS NO. Registered Holders
Bioactive peptides extracted from bovine thymus

Immunomodulatory drug. It has the function of regulating and enhancing the cellular immune function of the human body. It can promote the maturation of T lymphocytes in the peripheral blood after mitogen activation, increase the secretion of various lymphokines (such as alpha;, gamma; interferon, interleukin 2 and interleukin 3) after T cells are activated by various antigens or mitogens, and increase the level of lymphokine receptors on T cells. It also enhances lymphocyte response by activating T4 helper cells. In addition, this product may affect the chemotaxis of NK precursor cells, which become more cytotoxic after exposure to interferon. Therefore, this product has the function of regulating and enhancing the cellular immune function of the human body.

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Immunomodulatory drug. It has the function of regulating and enhancing the cellular immune function of the human body. It can promote the maturation of T lymphocytes in the peripheral blood after mitogen activation, increase the secretion of various lymphokines (such as alpha;, gamma; interferon, interleukin 2 and interleukin 3) after T cells are activated by various antigens or mitogens, and increase the level of lymphokine receptors on T cells. It also enhances lymphocyte response by activating T4 helper cells. In addition, this product may affect the chemotaxis of NK precursor cells, which become more cytotoxic after exposure to interferon. Therefore, this product has the function of regulating and enhancing the cellular immune function of the human body.

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Sophora flavescens ointment
Total Sophora flavescens alkaloids
Name Description Content CAS NO. Registered Holders
Sophora flavescens

Animal experiments show that this product has a certain antipruritic effect on guinea pig skin itching caused by histamine phosphate when applied externally to the skin. This product has a certain improvement effect on rats with Candida albicans vaginitis when administered vaginally.

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Animal experiments show that this product has a certain antipruritic effect on guinea pig skin itching caused by histamine phosphate when applied externally to the skin. This product has a certain improvement effect on rats with Candida albicans vaginitis when administered vaginally.

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Ranitidine Hydrochloride Capsules
Ranitidine hydrochloride, its chemical name is: N'-methyl-N-[2-[[[5-[(dimethylamino)methyl]-2-furyl]-methyl]thio]ethyl]-2-nitro-1,1-ethylenediamine hydrochloride.
Name Description Content CAS NO. Registered Holders
Ranitidine Hydrochloride

It competitively blocks the binding of histamine to H2 receptors and inhibits the action of gastric acid. Its molar potency is 5 to 12 times that of cimetidine, making it a potent H2 receptor blocker.

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It competitively blocks the binding of histamine to H2 receptors and inhibits the action of gastric acid. Its molar potency is 5 to 12 times that of cimetidine, making it a potent H2 receptor blocker.

66357-59-3 48
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