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Wuhan Zhengtong Pharmaceutical Co., Ltd.
  • Founded in:

    2011-05-17
  • Country:

    China China
  • Address:

    Room 1, 2nd Floor, Building B-3, No. 776, Huian Avenue, Cihui Office, Dongxihu District, Wuhan City (8)
  • Tax NO.:

    91420112574931779Q
  • Registered Funds:

    50 million yuan
  • Website:

  • Email:

Related Drugs
Sulfasalazine suppository
This product contains sulfasalazine.
Name Description Content CAS NO. Registered Holders
Sulfasalazine

Anti-inflammatory drugs. A pharmacological experiment on a rat immune ulcerative colitis model was conducted to compare the effects of anal suppositories and oral tablets in the treatment of colitis. The results showed that the therapeutic effect of anal suppositories was significantly better than oral administration.

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Anti-inflammatory drugs. A pharmacological experiment on a rat immune ulcerative colitis model was conducted to compare the effects of anal suppositories and oral tablets in the treatment of colitis. The results showed that the therapeutic effect of anal suppositories was significantly better than oral administration.

599-79-1 13
Metronidazole suppositories
Metronidazole.
Name Description Content CAS NO. Registered Holders
Metronidazole

This product is a nitroimidazole derivative that can inhibit the redox reaction of amoeba and break the nitrogen chain of the protozoa. In vitro tests have shown that when the drug concentration is 1~2mg/L, the histolytica amoeba can undergo morphological changes in 6~20 hours and all are killed within 24 hours. When the concentration is 0.2mg/L, the histolytica amoeba can be killed within 72 hours. This product has a strong effect of killing trichomonas, and its mechanism is unknown. Metronidazole has a killing effect on cells and anaerobic microorganisms growing under hypoxic conditions. The metabolites generated when it is reduced in the human body also have anti-anaerobic effects, inhibiting the synthesis of bacterial deoxyribonucleic acid, thereby interfering with the growth and reproduction of bacteria, and ultimately causing bacterial death.

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This product is a nitroimidazole derivative that can inhibit the redox reaction of amoeba and break the nitrogen chain of the protozoa. In vitro tests have shown that when the drug concentration is 1~2mg/L, the histolytica amoeba can undergo morphological changes in 6~20 hours and all are killed within 24 hours. When the concentration is 0.2mg/L, the histolytica amoeba can be killed within 72 hours. This product has a strong effect of killing trichomonas, and its mechanism is unknown. Metronidazole has a killing effect on cells and anaerobic microorganisms growing under hypoxic conditions. The metabolites generated when it is reduced in the human body also have anti-anaerobic effects, inhibiting the synthesis of bacterial deoxyribonucleic acid, thereby interfering with the growth and reproduction of bacteria, and ultimately causing bacterial death.

443-48-1 39
Diclofenac Sodium Suppository
The main component of this product and its chemical name is: 2-[(2,6-dichlorophenyl)amino]-phenylacetic acid sodium. Its structural formula is: Molecular formula: C14H10CI2NNaO2; Molecular weight: 318.13
Name Description Content CAS NO. Registered Holders
Diclofenac sodium

This product is a derivative of ibufenac, and its analgesic, anti-inflammatory and antipyretic effects are 2-2.5 times stronger than indomethacin and 26-50 times stronger than aspirin. The analgesic and anti-inflammatory effects of this product are achieved by inhibiting cyclooxygenase to reduce prostaglandins and also by inhibiting lipoxygenates to reduce the products of leukotrienes, bradykinin, etc.

More

This product is a derivative of ibufenac, and its analgesic, anti-inflammatory and antipyretic effects are 2-2.5 times stronger than indomethacin and 26-50 times stronger than aspirin. The analgesic and anti-inflammatory effects of this product are achieved by inhibiting cyclooxygenase to reduce prostaglandins and also by inhibiting lipoxygenates to reduce the products of leukotrienes, bradykinin, etc.

15307-79-6 55
Diclofenac Sodium Suppository
The main ingredient and chemical name of this product are: Sodium 2-[(2,6-dichlorophenyl)amino]-phenylacetate
Name Description Content CAS NO. Registered Holders
Diclofenac sodium

This product is a derivative of ibufenac, and its analgesic, anti-inflammatory and antipyretic effects are 2-2.5 times stronger than indomethacin and 26-50 times stronger than aspirin. The analgesic and anti-inflammatory effects of this product are achieved by inhibiting cyclooxygenase to reduce prostaglandins and also by inhibiting lipoxygenates to reduce the products of leukotrienes, bradykinin, etc.

More

This product is a derivative of ibufenac, and its analgesic, anti-inflammatory and antipyretic effects are 2-2.5 times stronger than indomethacin and 26-50 times stronger than aspirin. The analgesic and anti-inflammatory effects of this product are achieved by inhibiting cyclooxygenase to reduce prostaglandins and also by inhibiting lipoxygenates to reduce the products of leukotrienes, bradykinin, etc.

15307-79-6 55
Nitrofurantoin suppositories
This product is a compound preparation, containing 0.75 mg of dexamethasone acetate, 10 mg of camphor, and 10 mg of menthol per gram. The auxiliary material is an emulsion matrix.
Name Description Content CAS NO. Registered Holders
Dexamethasone-17-acetate

0.75mg 1177-87-3 13
D-CAMPHOR

10mg 464-49-3 2
DL-Menthol

10mg 89-78-1 8
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