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Hainan Haishen Tongzhou Pharmaceutical Co., Ltd.

  • Founded in:

    1993-08-03
  • Country:

    China China
  • Address:

    No. 6, Yaogu 2nd Road, Yaogu Industrial Park, National High-tech Zone, Haikou City, Hainan Province
  • Tax NO.:

    91460100283995932K
  • Registered Funds:

    10.5 million yuan
  • Website:

  • Email:

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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, blocking the transfer RNA (t-RNA) from binding to the site, and also blocking the transfer of the polypeptide chain from the acceptor site to the site, thereby inhibiting bacterial protein synthesis.

80214-83-1 28
Roxithromycin Dispersible Tablets
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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, blocking the transfer RNA (t-RNA) from binding to the site, and also blocking the transfer of the polypeptide chain from the acceptor site to the 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, blocking the transfer RNA (t-RNA) from binding to the site, and also blocking the transfer of the polypeptide chain from the acceptor site to the site, thereby inhibiting bacterial protein synthesis.

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