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YANGTZE River Pharmaceutical Group Shanghai HAI-NI Pharmaceutical Co., Ltd.
  • Founded in:

    2001-01-08
  • Country:

    China China
  • Address:

    No. 3999, Hunan Road, Zhoupu Town, Pudong New Area
  • Tax NO.:

    91310115132179436W
  • Registered Funds:

    110 million yuan
  • Website:

  • Email:

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Xianhuang Granules
Rehmannia root, yam, wolfberry, eucommia bark, dodder seed, curculigo, codonopsis pilosula, astragalus, salvia miltiorrhiza, yanhusuo (made with vinegar), oyster (calcined).
Name Description Content CAS NO. Registered Holders
REHMANNIAE RADIX PRAEPARATA

0
Wild Yam P.E Diosgenine 7%-16%

0
lycii Fructus

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Eucommia

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Cuscutae Semen

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curculigo

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Codonopsis

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Astragali Radix

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Salvia Root P.E Tanshinone IIA 20%

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Yanhusuo (vinegar-made)

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Oyster (calcined)

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Cough capsules
Ephedra, Perilla Seed, Magnolia Bark (fried with ginger), Ledebouriella Seed, Fritillaria Bulbus Fritillariae Citrus (fried with sand), Ginkgo, Poppy Shell, Borax, Citrus Aurantium (fried with bran), Tangerine Peel, Platycodon, Saposhnikovia, Poria, White Head, Peucedanum, Licorice, Mulberry Leaf, Scutellaria Baicalensis (fried with wine), Adenophora australis, Mint, Perilla Leaf.
Name Description Content CAS NO. Registered Holders
Platycodonis Radix

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Folia perillae acutae

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PEPPERMINT

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Adenophorae Radix

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Scutellaria baicalensis (roasted with wine)

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Mori Folium

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DGL

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PEUCEDANI RADIX

0
CYNANCHI STAUNTONII RHIZOMA ET RADIX

0
Poria

0
SAPOSHNIKOVIAE RADIX

0
Ephedra

0
Citri reticulatae pericarpium

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Citrus aurantium (fried with bran)

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Sodium tetraborate decahydrate

1303-96-4 15
PAPAVERIS PERICARPIUM

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ginkgo

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French Pinellia (fried with sand)

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Dehydroandrographolide

134418-28-3 0
Tinglizi (solitary vegetable)

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Magnolia officinalis (roasted with ginger)

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Perillae Fructus

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Donepezil Hydrochloride Capsules
Donepezil hydrochloride chemical name: l-benzyl-4-[(5,6-dimethoxy-1-indanone-2-yl)methyl]piperidine hydrochloride.
Name Description Content CAS NO. Registered Holders
Donepezil Hydrochloride

No specific pharmacological information is provided

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No specific pharmacological information is provided

120011-70-3 41
Gatifloxacin Capsules
The main ingredient of this product is gatifloxacin, chemical name: (±)-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(-3-methyl-1-piperazine)-4-keto-3-quinolinecarboxylic acid sesquihydrate. Chemical structure: Molecular formula: C19H22FN3O4·1.5H2O Molecular weight: 402.42
Name Description Content CAS NO. Registered Holders
Gatifloxacin

By inhibiting bacterial DNA gyrase and topoisomerase IV, it inhibits bacterial DNA replication, transcription, and repair processes. It has antibacterial activity against the following microorganisms: Gram-positive bacteria (such as Staphylococcus aureus, Streptococcus pneumoniae, etc.), Gram-negative bacteria (such as Haemophilus, Moraxella catarrhalis, Neisseria, Acinetobacter, Klebsiella pneumoniae, Pseudomonas aeruginosa, etc.) and other microorganisms (such as Chlamydia pneumoniae, Legionella pneumophila, Mycoplasma pneumoniae).

More

By inhibiting bacterial DNA gyrase and topoisomerase IV, it inhibits bacterial DNA replication, transcription, and repair processes. It has antibacterial activity against the following microorganisms: Gram-positive bacteria (such as Staphylococcus aureus, Streptococcus pneumoniae, etc.), Gram-negative bacteria (such as Haemophilus, Moraxella catarrhalis, Neisseria, Acinetobacter, Klebsiella pneumoniae, Pseudomonas aeruginosa, etc.) and other microorganisms (such as Chlamydia pneumoniae, Legionella pneumophila, Mycoplasma pneumoniae).

112811-59-3 20
Gatifloxacin Injection
Gatifloxacin, chemical name 1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methylpiperazinyl)-4-oxo-3-quinolinecarboxylic acid.
Name Description Content CAS NO. Registered Holders
Gatifloxacin

It inhibits bacterial DNA replication, transcription and repair processes by inhibiting bacterial DNA gyrase and topoisomerase IV. It has antibacterial activity against the following microorganisms: Gram-positive bacteria (such as Staphylococcus aureus, Streptococcus pneumoniae), Gram-negative bacteria (such as Escherichia coli, Haemophilus influenzae and parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis, Neisseria gonorrhoeae, Proteus mirabilis) and other microorganisms (such as Chlamydia pneumoniae, Legionella pneumophila, Mycoplasma pneumoniae).

More

It inhibits bacterial DNA replication, transcription and repair processes by inhibiting bacterial DNA gyrase and topoisomerase IV. It has antibacterial activity against the following microorganisms: Gram-positive bacteria (such as Staphylococcus aureus, Streptococcus pneumoniae), Gram-negative bacteria (such as Escherichia coli, Haemophilus influenzae and parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis, Neisseria gonorrhoeae, Proteus mirabilis) and other microorganisms (such as Chlamydia pneumoniae, Legionella pneumophila, Mycoplasma pneumoniae).

112811-59-3 20
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