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Nanchang Feihong Pharmaceutical Co., Ltd.
  • Founded in:

    1996-06-13
  • Country:

    China China
  • Address:

    No. 388, Gaoxin 5th Road, High-tech Industrial Development Zone, Nanchang City, Jiangxi Province
  • Tax NO.:

    91360100158404187P
  • Registered Funds:

    10 million yuan
  • Email:

Related Drugs
Ferrous Lactate Tablets
Structural formula: Ferrous lactate Molecular formula: C6H10FeO6·3H2O Molecular weight: 288.04
Name Description Content CAS NO. Registered Holders
Ferrous lactate

Iron is an indispensable element for the human body and is an important component of hemoglobin, myoglobin and various tissue enzymes. Iron deficiency can cause iron deficiency anemia or other iron deficiency diseases. Ferrous lactate has a high absorption rate and can be used as an iron supplement.

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Iron is an indispensable element for the human body and is an important component of hemoglobin, myoglobin and various tissue enzymes. Iron deficiency can cause iron deficiency anemia or other iron deficiency diseases. Ferrous lactate has a high absorption rate and can be used as an iron supplement.

5905-52-2 2
Oyster Calcium Carbonate Chewable Tablets
Main ingredients: oyster calcium carbonate; auxiliary ingredients: sucrose, citric acid, magnesium stearate, pigment (tartrazine).
Name Description Content CAS NO. Registered Holders
Oyster calcium carbonate

Participates in bone formation and reconstruction of bone tissue after fracture, as well as muscle contraction, nerve transmission, coagulation mechanism and reduces capillary permeability, etc.

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Participates in bone formation and reconstruction of bone tissue after fracture, as well as muscle contraction, nerve transmission, coagulation mechanism and reduces capillary permeability, etc.

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Nimesulide Dispersible Tablets
This product mainly contains nimesulide.
Name Description Content CAS NO. Registered Holders
Nimesulide

This product is a non-steroidal anti-inflammatory drug with anti-inflammatory, analgesic and antipyretic effects. Its mechanism of action is not yet fully understood, but it may be mainly related to the inhibition of prostaglandin synthesis, mediator release of leukocytes and oxidative reactions of polymorphonuclear leukocytes.

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This product is a non-steroidal anti-inflammatory drug with anti-inflammatory, analgesic and antipyretic effects. Its mechanism of action is not yet fully understood, but it may be mainly related to the inhibition of prostaglandin synthesis, mediator release of leukocytes and oxidative reactions of polymorphonuclear leukocytes.

51803-78-2 14
Acyclovir dispersible tablets
The main ingredient of this product is acyclovir, whose chemical name is 9-(2-hydroxyethoxymethyl)guanine.
Name Description Content CAS NO. Registered Holders
Acyclovir

Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells.

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Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells.

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Indapamide Tablets
The main ingredient and chemical name of this product is indapamide, and its chemical name is N-(2-methyl-2,3-dihydro-1H-indolyl)-3-sulfamoyl-4-chloro-benzamide. Molecular formula: C16H16CIN3O3S Molecular weight: 365.83
Name Description Content CAS NO. Registered Holders
Indapamide

It is a sulfonamide diuretic that works by inhibiting the reabsorption of water and electrolytes in the dilution segment of the distal renal tubular cortex. The mechanism of blood pressure reduction is unknown, but possible mechanisms include regulating calcium influx into vascular smooth muscle cells; stimulating the synthesis of prostaglandins PGE2 and prostaglandins PGI2; and reducing vascular hypersensitivity to vasopressors, thereby inhibiting vasoconstriction. This product has little or no effect on cardiac output, heart rate and rhythm when lowering blood pressure. Long-term use of this product rarely affects glomerular filtration rate or renal blood flow. This drug does not affect the metabolism of blood lipids and carbohydrates.

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It is a sulfonamide diuretic that works by inhibiting the reabsorption of water and electrolytes in the dilution segment of the distal renal tubular cortex. The mechanism of blood pressure reduction is unknown, but possible mechanisms include regulating calcium influx into vascular smooth muscle cells; stimulating the synthesis of prostaglandins PGE2 and prostaglandins PGI2; and reducing vascular hypersensitivity to vasopressors, thereby inhibiting vasoconstriction. This product has little or no effect on cardiac output, heart rate and rhythm when lowering blood pressure. Long-term use of this product rarely affects glomerular filtration rate or renal blood flow. This drug does not affect the metabolism of blood lipids and carbohydrates.

26807-65-8 28
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