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Shanghai Fudan Fuhua Pharmaceutical Co., Ltd.
  • Founded in:

    1981-12-01
  • Country:

    China China
  • Address:

    No. 1399 Shuguang Road, Minhang District, Shanghai
  • Tax NO.:

    91310112132661556L
  • Registered Funds:

    44.8 million yuan
  • Email:

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Huperzine A Capsules
The active ingredient of this product is Huperzine A, and the excipients are starch, lactose, and talc. Chemical name: (5R, 9R, 11E)-5-amino-11ethylidene-5,8,9,10-tetrahydro-7-methyl-5,9-methylenecyclooctatetraen[b]pyridine-2(1H)-one. Chemical structure: Molecular formula: C15H18N2O Molecular weight: 242.32
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(-)-Huperzine A

This product is a cholinesterase inhibitor, which has a selective inhibitory effect on acetylcholinesterase and is easy to cross the blood-brain barrier. It has the effect of promoting memory retrieval and enhancing memory retention.

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Tamoxifen Citrate Tablets
The main chemical component of this product is tamoxifen citrate. The chemical name is: (Z)-N, N-dimethyl-2-[4-(1,2-diphenyl-1-butenyl)phenoxy]-ethylamine citrate. Molecular formula: C26H29NOC6H8O7. Molecular weight: 563.65
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Tamoxifen citrate

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Tamoxifen is a non-steroidal anti-estrogen drug. Its Z isomer competes with estrogen receptors to form a receptor complex, blocking the effects of estrogen and thus inhibiting the proliferation of breast cancer cells.

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Tiapride Hydrochloride Tablets
The main ingredient of this product is tiapride hydrochloride.
Name Description Content CAS NO. Registered Holders
Tiapride hydrochloride

This product belongs to the benzamide antipsychotic drug, which has an inhibitory effect on the hyperfunction of dopaminergic nerves in the midbrain limbic system and an antagonistic effect on dopaminergic nerve movement disorders in the striatum, thereby producing a calming and sedative effect. It is characterized by its good effect on sensory and motor neurological diseases and psychomotor behavioral disorders. Animal experiments have confirmed that this product can block the conduction of pain impulses through the spinal thalamic tract to the reticular formation. The analgesic effect of this drug may be related to the integration of pain impulses by the thalamus. In addition, it has an antiemetic effect.

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This product belongs to the benzamide antipsychotic drug, which has an inhibitory effect on the hyperfunction of dopaminergic nerves in the midbrain limbic system and an antagonistic effect on dopaminergic nerve movement disorders in the striatum, thereby producing a calming and sedative effect. It is characterized by its good effect on sensory and motor neurological diseases and psychomotor behavioral disorders. Animal experiments have confirmed that this product can block the conduction of pain impulses through the spinal thalamic tract to the reticular formation. The analgesic effect of this drug may be related to the integration of pain impulses by the thalamus. In addition, it has an antiemetic effect.

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Ofloxacin Tablets
The chemical name of this product is (±)-9-fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid, and its molecular weight is 361.37.
Name Description Content CAS NO. Registered Holders
(±)-9-Fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid

This product has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacilli, and has high antibacterial activity against penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae, and Moraxella. It has antibacterial activity against most strains of Pseudomonas, such as Pseudomonas aeruginosa. It has antibacterial activity against methicillin-sensitive Staphylococci, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus, and Enterococcus faecalis. It has good antimicrobial effects against Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. Ofloxacin is a bactericide that acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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This product has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacilli, and has high antibacterial activity against penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae, and Moraxella. It has antibacterial activity against most strains of Pseudomonas, such as Pseudomonas aeruginosa. It has antibacterial activity against methicillin-sensitive Staphylococci, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus, and Enterococcus faecalis. It has good antimicrobial effects against Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. Ofloxacin is a bactericide that acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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Ofloxacin Tablets
The chemical name of this product is (±)-9-fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid, and its molecular weight is 361.37.
Name Description Content CAS NO. Registered Holders
(±)-9-Fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid

It has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacteria, and has antibacterial activity against most bacteria of the Enterobacteriaceae family, penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae and Moraxella, Pseudomonas aeruginosa, etc. It has antibacterial activity against methicillin-sensitive Staphylococcus aureus, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus and Enterococcus faecalis. It has good antimicrobial effects on Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. It acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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It has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacteria, and has antibacterial activity against most bacteria of the Enterobacteriaceae family, penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae and Moraxella, Pseudomonas aeruginosa, etc. It has antibacterial activity against methicillin-sensitive Staphylococcus aureus, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus and Enterococcus faecalis. It has good antimicrobial effects on Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. It acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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