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Jiangxi Pharmaceutical Co., Ltd.
  • Founded in:

    1996-06-10
  • Country:

    China China
  • Address:

    No. 758, Huiren West Avenue, Xiaolan Industrial Park, Nanchang County, Nanchang City, Jiangxi Province
  • Tax NO.:

    913600001582615429
  • Registered Funds:

    295.8 million yuan
  • Website:

  • Email:

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Neomycin Sulfate Injection
Micromycin sulfate. Its chemical name is: O-2-amino-2,3,4,5-tetradeoxy-5-(methylamino)-2-D-erythro-hexopyranosyl-(1rarr;4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1rarr;6)-2-deoxy-D-streptamine sulfate.
Name Description Content CAS NO. Registered Holders
MICRONOMICIN SULFATE

This product is an aminoglycoside antibiotic with an antibacterial spectrum similar to that of gentamicin. It has antibacterial effects on a variety of Gram-negative bacteria and Staphylococcus aureus (including beta-lactamase-producing strains); Streptococci, anaerobic bacteria, Mycobacterium tuberculosis, Rickettsia, viruses and fungi are resistant to this product. This product is stable to aminoglycoside acetyltransferase AAC (6) produced by bacteria, with a minimum inhibitory concentration of 0.1 to 6.25 mg/L. The mechanism of action is to bind to the 30S subunit of the bacterial ribosome and inhibit the synthesis of bacterial proteins.

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This product is an aminoglycoside antibiotic with an antibacterial spectrum similar to that of gentamicin. It has antibacterial effects on a variety of Gram-negative bacteria and Staphylococcus aureus (including beta-lactamase-producing strains); Streptococci, anaerobic bacteria, Mycobacterium tuberculosis, Rickettsia, viruses and fungi are resistant to this product. This product is stable to aminoglycoside acetyltransferase AAC (6) produced by bacteria, with a minimum inhibitory concentration of 0.1 to 6.25 mg/L. The mechanism of action is to bind to the 30S subunit of the bacterial ribosome and inhibit the synthesis of bacterial proteins.

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Neomycin Sulfate Injection
Streptavidin sulfate. Its chemical name is: O-2-amino-2,3,4,5-tetrateoxy-5-(methylamino)-2-D-erythro-hexopyranosyl-(14)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(16)-2-deoxy-D-streptamine sulfate.
Name Description Content CAS NO. Registered Holders
MICRONOMICIN SULFATE

This product is an aminoglycoside antibiotic. The antibacterial spectrum is similar to that of gentamicin. It has antibacterial effects on Gram-negative bacteria such as Escherichia coli, aerogenes, Klebsiella, Proteus mirabilis, some indole-positive Proteus, Pseudomonas aeruginosa, some Neisseria, some non-pigmented Serratia and Shigella. Among Gram-positive bacteria, Staphylococcus aureus (including beta-lactamase-producing strains) is sensitive to this product; Streptococci (including Streptococcus pyogenes, Pneumococcus, Streptococcus faecalis, etc.) are all resistant to this product. Anaerobic bacteria (Bacteroides), Mycobacterium tuberculosis, Rickettsia, viruses and fungi are also resistant to this product. This product is stable to aminoglycoside acetyltransferase AAC (6) produced by bacteria, so it still has antibacterial activity against bacteria that are resistant to kanamycin, gentamicin, amikacin, ribosomycin, etc. due to the production of this enzyme. The minimum inhibitory concentration of this product is 0.1-6.25 mg/L. The mechanism of action of this product is to bind to the bacterial ribosome 30S subunit and inhibit the synthesis of bacterial protein.

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This product is an aminoglycoside antibiotic. The antibacterial spectrum is similar to that of gentamicin. It has antibacterial effects on Gram-negative bacteria such as Escherichia coli, aerogenes, Klebsiella, Proteus mirabilis, some indole-positive Proteus, Pseudomonas aeruginosa, some Neisseria, some non-pigmented Serratia and Shigella. Among Gram-positive bacteria, Staphylococcus aureus (including beta-lactamase-producing strains) is sensitive to this product; Streptococci (including Streptococcus pyogenes, Pneumococcus, Streptococcus faecalis, etc.) are all resistant to this product. Anaerobic bacteria (Bacteroides), Mycobacterium tuberculosis, Rickettsia, viruses and fungi are also resistant to this product. This product is stable to aminoglycoside acetyltransferase AAC (6) produced by bacteria, so it still has antibacterial activity against bacteria that are resistant to kanamycin, gentamicin, amikacin, ribosomycin, etc. due to the production of this enzyme. The minimum inhibitory concentration of this product is 0.1-6.25 mg/L. The mechanism of action of this product is to bind to the bacterial ribosome 30S subunit and inhibit the synthesis of bacterial protein.

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Acacia tablets
Each tablet of this product mainly contains aspirin and caffeine.
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Acetylsalicylic acid

Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Inhibits prostaglandin synthesis and has antipyretic and analgesic effects

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Caffeine

Central nervous system stimulant, can enhance the antipyretic and analgesic effects of the above drugs

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Central nervous system stimulant, can enhance the antipyretic and analgesic effects of the above drugs

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Atropine Sulfate Tablets
The main ingredient of this product is atropine. Chemical name: alpha;-(hydroxymethyl)phenylacetic acid 8-methyl-8-azabicyclo[3,2,1]-3-octyl ester sulfate monohydrate Molecular weight: C34H46N2O6.H2SO4.H2O
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Atropine

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alpha;-(Hydroxymethyl)phenylacetic acid 8-methyl-8-azabicyclo[3,2,1]-3-octyl ester sulfate monohydrate Molecular weight: C34H46N2O6.H2SO4.H2O

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Haloperidol Tablets
The main ingredient of this product is haloperidol, and its chemical name is: 1-(4-fluorophenyl)-4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]-1-butanone.
Name Description Content CAS NO. Registered Holders
Haloperidol

This product belongs to the butyrophenone antipsychotic drug. Its antipsychotic effect is related to its ability to block dopamine receptors in the brain and promote the conversion of dopamine in the brain. It has a good effect on resisting hallucinations and delusions and excitement and agitation, has a strong effect in blocking extrapyramidal dopamine, and also has a strong antiemetic effect, but its sedative effect and blocking effects on adrenaline receptors and cholinergic receptors are weak.

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This product belongs to the butyrophenone antipsychotic drug. Its antipsychotic effect is related to its ability to block dopamine receptors in the brain and promote the conversion of dopamine in the brain. It has a good effect on resisting hallucinations and delusions and excitement and agitation, has a strong effect in blocking extrapyramidal dopamine, and also has a strong antiemetic effect, but its sedative effect and blocking effects on adrenaline receptors and cholinergic receptors are weak.

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