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ShanxiTongda Pharmaceutical Co., Ltd.
  • Founded in:

    1997-05-30
  • Country:

    China China
  • Address:

    The First Pharmaceutical Industrial Park, Datong Economic Development Zone
  • Tax NO.:

    911402006020035321
  • Registered Funds:

    50 million yuan
  • Website:

  • Email:

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Aminopyrine Caffeine Tablets
The content of aminopyrine (C13H17N3O) in this product should be 95.0% to 105.0% of the labeled amount; the content of caffeine (C8H10N4O2) should be 90.0% to 110.0% of the labeled amount.
Name Description Content CAS NO. Registered Holders
Aminopyrine

95.0%~105.0%Label quantity 0
Caffeine

90.0%~110.0%Label quantity 0
Miconazole nitrate suppository
Each tablet of this product contains 0.2 grams of miconazole nitrate as the main ingredient and stearic acid as the auxiliary ingredient.
Name Description Content CAS NO. Registered Holders
Miconazole nitrate

This product is a broad-spectrum antifungal drug that has antibacterial effects on a variety of fungi, especially Candida albicans, and also has antibacterial effects on certain Gram-positive bacteria. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes.

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This product is a broad-spectrum antifungal drug that has antibacterial effects on a variety of fungi, especially Candida albicans, and also has antibacterial effects on certain Gram-positive bacteria. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes.

0.2g 22832-87-7 31
Glycerol tristearate

This product is a broad-spectrum antifungal drug that has antibacterial effects on a variety of fungi, especially Candida albicans, and also has antibacterial effects on certain Gram-positive bacteria. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes.

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This product is a broad-spectrum antifungal drug that has antibacterial effects on a variety of fungi, especially Candida albicans, and also has antibacterial effects on certain Gram-positive bacteria. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes.

555-43-1 1
Spirulina Tablets
Spirulina.
Name Description Content CAS NO. Registered Holders
SPIRULINA POWDER

724424-92-4 0
Amoxicillin and Clavulanate Potassium Tablets
Amoxicillin 0.25g and clavulanic acid 0.0625g.
Name Description Content CAS NO. Registered Holders
Amoxicillin

Broad-spectrum penicillin antibiotics, when used in combination with clavulanic acid, can protect it from hydrolysis by β-lactamase, and have a good effect on enzyme-producing Staphylococcus aureus, Staphylococcus epidermidis and other bacteria.

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Broad-spectrum penicillin antibiotics, when used in combination with clavulanic acid, can protect it from hydrolysis by β-lactamase, and have a good effect on enzyme-producing Staphylococcus aureus, Staphylococcus epidermidis and other bacteria.

0.25g 26787-78-0 30
Clavulanic acid

It has a strong broad-spectrum β-lactamase inhibitory effect and has only weak antibacterial activity itself. Its antibacterial spectrum can be expanded when used in combination with amoxicillin.

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It has a strong broad-spectrum β-lactamase inhibitory effect and has only weak antibacterial activity itself. Its antibacterial spectrum can be expanded when used in combination with amoxicillin.

0.0625g 58001-44-8 0
Roxithromycin Dispersible Tablets
The main component of this product is roxithromycin. 9-(O-[(2-methoxyethoxy)-methyl]oxime)erythromycin.
Name Description Content CAS NO. Registered Holders
Roxithromycin

This product is a semi-synthetic 14-membered macrolide antibiotic. Its antibacterial spectrum and antibacterial effect are basically similar to those of erythromycin. It is slightly less effective than erythromycin against Gram-positive bacteria, but stronger than erythromycin against Legionella pneumophila. Its antimicrobial effect against Chlamydia pneumoniae, Mycoplasma pneumoniae, and Ureaplasma urealyticum is similar to or slightly stronger than that of erythromycin. This product can penetrate the bacterial cell membrane and reversibly bind to the 50S subunit of the bacterial ribosome near the donor (P site), blocking the transfer RNA (t-RNA) from binding to the P site, and also blocking the transfer of the polypeptide chain from the acceptor site (A site) to the P site, thereby inhibiting bacterial protein synthesis.

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This product is a semi-synthetic 14-membered macrolide antibiotic. Its antibacterial spectrum and antibacterial effect are basically similar to those of erythromycin. It is slightly less effective than erythromycin against Gram-positive bacteria, but stronger than erythromycin against Legionella pneumophila. Its antimicrobial effect against Chlamydia pneumoniae, Mycoplasma pneumoniae, and Ureaplasma urealyticum is similar to or slightly stronger than that of erythromycin. This product can penetrate the bacterial cell membrane and reversibly bind to the 50S subunit of the bacterial ribosome near the donor (P site), blocking the transfer RNA (t-RNA) from binding to the P site, and also blocking the transfer of the polypeptide chain from the acceptor site (A site) to the P site, thereby inhibiting bacterial protein synthesis.

80214-83-1 28
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