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Changchun City XinAn Pharmaceutical Group Co., Ltd.
  • Founded in:

    2002-06-11
  • Country:

    China China
  • Address:

    Changchun Helong Economic Development Zone
  • Tax NO.:

    91220101735927085J
  • Registered Funds:

    125 million yuan
  • Email:

Related Drugs
Anti-bone hyperplasia pills
Rehmannia root, Cistanche deserticola (steamed), Epimedium, Millettia reticulata, Achyranthes bidentata, etc.
Name Description Content CAS NO. Registered Holders
REHMANNIAE RADIX PRAEPARATA

0
Cistanche deserticola (steamed)

0
Epimedium P.E Icariin 10%,20% HPLC

0
Spatholobi Caulis

0
Achyranthis bidentatae radix

0
Chuanke Ning Tablets
Ephedra, pig bile, bitter almond powder, platycodon, and licorice.
Name Description Content CAS NO. Registered Holders
Ephedra

0
GALL

8008-63-7 0
Bitter almond cream

0
Platycodonis Radix

0
DGL

0
Calcium Gluconate Lozenges
Each tablet of this product contains the main ingredient calcium gluconate. The auxiliary ingredients are sucrose, tartrazine, flavor, talcum powder and magnesium stearate.
Name Description Content CAS NO. Registered Holders
CALCIUM GLUCONATE MONOHYDRATE

Participates in the formation of bones and the reconstruction of bone tissue after fracture, muscle contraction, nerve transmission, coagulation process and reduces the permeability of capillaries, etc.

More

Participates in the formation of bones and the reconstruction of bone tissue after fracture, muscle contraction, nerve transmission, coagulation process and reduces the permeability of capillaries, etc.

66905-23-5 33
Compound Hericium Granules
Hericium erinaceus fruiting body, sucralfate, bismuth subnitrate, magnesium trisilicate.
Name Description Content CAS NO. Registered Holders
Hericium erinaceus fruiting body

0
Sucralfate

54182-58-0 22
Bismuth subnitrate

1304-85-4 17
Magnesium trisilicate

14987-04-3 11
Erythromycin Ethylsuccinate Granules
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.

More

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
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