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Heilongjiang Fuhe Pharmaceutical Group Co., Ltd.
  • Founded in:

    1994-12-28
  • Country:

    China China
  • Address:

    No. 1166, Zhengyang Street, Zhaodong City, Suihua City, Heilongjiang Province
  • Tax NO.:

    912312001313217015
  • Registered Funds:

    78.54 million yuan
  • Website:

  • Email:

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Ambroxol Hydrochloride and Glucose Injection
trans-4-[(2-amino-3,5-dibromobenzyl)amino]cyclohexanol hydrochloride
Name Description Content CAS NO. Registered Holders
trans-4-[(2-amino-3,5-dibromobenzyl)amino]cyclohexanol hydrochloride

This product has the characteristics of promoting mucus elimination and dissolving secretions. It can promote the elimination of viscous secretions in the respiratory tract and reduce mucus retention, significantly promote expectoration, and improve respiratory conditions. When using this product for treatment, the patient's mucus secretion can return to normal, cough and sputum volume are usually significantly reduced, and the surfactant on the respiratory mucosa can thus play its normal protective function. In the acute toxicity test, the toxicity index of ambroxol hydrochloride is very low, and it has no mutagenicity and carcinogenicity.

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This product has the characteristics of promoting mucus elimination and dissolving secretions. It can promote the elimination of viscous secretions in the respiratory tract and reduce mucus retention, significantly promote expectoration, and improve respiratory conditions. When using this product for treatment, the patient's mucus secretion can return to normal, cough and sputum volume are usually significantly reduced, and the surfactant on the respiratory mucosa can thus play its normal protective function. In the acute toxicity test, the toxicity index of ambroxol hydrochloride is very low, and it has no mutagenicity and carcinogenicity.

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Erythromycin Ethylsuccinate Tablets
The main ingredient of this product is erythromycin ethylsuccinate.
Name Description Content CAS NO. Registered Holders
Erythromycin ethylsuccinate

This product belongs to the macrolide antibiotics, which is the ethyl succinate of erythromycin. It is more stable than erythromycin in gastric acid. It has antibacterial activity against Staphylococcus (except methicillin-resistant strains), various groups of streptococci and Gram-positive bacilli. Neisseria, Haemophilus influenzae, Bordetella pertussis, etc. are also sensitive to this product. This product also has antibacterial effects on various anaerobic bacteria except Bacteroides fragilis and Fusobacterium. It also has inhibitory effects on Legionella, Campylobacter fetus, some spirochetes, Mycoplasma pneumoniae, Rickettsia and Chlamydia. This product is an antibacterial agent, but it also has a bactericidal effect on some bacteria at high concentrations. This product can penetrate the bacterial cell membrane and form a reversible bond with the 50S subunit of the bacterial ribosome near the donor site (P site), blocking the transfer RNA (t-RNA) from binding to the P site, and also blocking the displacement 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 belongs to the macrolide antibiotics, which is the ethyl succinate of erythromycin. It is more stable than erythromycin in gastric acid. It has antibacterial activity against Staphylococcus (except methicillin-resistant strains), various groups of streptococci and Gram-positive bacilli. Neisseria, Haemophilus influenzae, Bordetella pertussis, etc. are also sensitive to this product. This product also has antibacterial effects on various anaerobic bacteria except Bacteroides fragilis and Fusobacterium. It also has inhibitory effects on Legionella, Campylobacter fetus, some spirochetes, Mycoplasma pneumoniae, Rickettsia and Chlamydia. This product is an antibacterial agent, but it also has a bactericidal effect on some bacteria at high concentrations. This product can penetrate the bacterial cell membrane and form a reversible bond with the 50S subunit of the bacterial ribosome near the donor site (P site), blocking the transfer RNA (t-RNA) from binding to the P site, and also blocking the displacement of the polypeptide chain from the acceptor site (A site) to the P site, thereby inhibiting bacterial protein synthesis.

1264-62-6 25
Ketoprofen Tablets
beta;-Methyl-(3-benzoyl)phenylacetic acid is also known as ketoprofen.
Name Description Content CAS NO. Registered Holders
beta;-methyl-(3-benzoyl)phenylacetic acid (ketoprofen)

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Ketoprofen Tablets
beta;-Methyl-(3-benzoyl)phenylacetic acid is also known as ketoprofen.
Name Description Content CAS NO. Registered Holders
beta;-methyl-(3-benzoyl)phenylacetic acid (ketoprofen)

Not yet clear

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Prostate Shule Tablets
Epimedium, Astragalus, Pollen Typhae, Plantain, and Cyathula.
Name Description Content CAS NO. Registered Holders
Epimedium P.E Icariin 10%,20% HPLC

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Astragali Radix

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POLLEN TYPHAE

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HERBA PLANTAGINIS

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Cyathulae Radix

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