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Yunnan Dianchi Pharmaceutical Co., Ltd.
  • Founded in:

    2002-01-10
  • Country:

    China China
  • Address:

    Zhuangdian Pharmaceutical Park, Chuxiong High-tech Zone, Yunnan Province
  • Tax NO.:

    915304027342981338
  • Registered Funds:

    19.8 million yuan
  • Email:

Related Drugs
Phellodendron chinense tablets
Palmitoyl hydrochloride.
Name Description Content CAS NO. Registered Holders
Palmitoyl Hydrochloride

1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.

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1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.

0
Phellodendron chinense tablets
Palmitoyl hydrochloride.
Name Description Content CAS NO. Registered Holders
Palmitoyl Hydrochloride

1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.

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1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.

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Phenolamine tablets
This product is a compound preparation, its components are: acetaminophen 0.15g, aminopyrine 0.1g, caffeine 30mg, chlorpheniramine maleate 2mg.
Name Description Content CAS NO. Registered Holders
Acetaminophen

It is a peripheral analgesic. Its mechanism of action is to inhibit the synthesis and release of prostaglandins (PGE1) in the hypothalamic temperature regulation center, thereby causing peripheral vasodilation and sweating to achieve an antipyretic effect. At the same time, it can inhibit the effects of PGE1, bradykinin and histamine, increase the pain threshold and produce analgesic effect.

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It is a peripheral analgesic. Its mechanism of action is to inhibit the synthesis and release of prostaglandins (PGE1) in the hypothalamic temperature regulation center, thereby causing peripheral vasodilation and sweating to achieve an antipyretic effect. At the same time, it can inhibit the effects of PGE1, bradykinin and histamine, increase the pain threshold and produce analgesic effect.

0.15g 103-90-2 68
Aminopyrine

It can inhibit the synthesis and release of prostaglandins in the hypothalamus, restore the normal responsiveness of the receptor neurons in the body temperature regulation center and have an antipyretic effect; at the same time, it also has an analgesic effect by inhibiting the synthesis of prostaglandins, etc., and can inhibit the synthesis and release of prostaglandins in local inflammatory tissues, stabilize lysosomal enzymes, and affect the phagocytic function of macrophages to have an anti-inflammatory effect.

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It can inhibit the synthesis and release of prostaglandins in the hypothalamus, restore the normal responsiveness of the receptor neurons in the body temperature regulation center and have an antipyretic effect; at the same time, it also has an analgesic effect by inhibiting the synthesis of prostaglandins, etc., and can inhibit the synthesis and release of prostaglandins in local inflammatory tissues, stabilize lysosomal enzymes, and affect the phagocytic function of macrophages to have an anti-inflammatory effect.

0.1g 0
Caffeine

It is a central nervous system stimulant that can excite the cerebral cortex, increase sensitivity to the outside world, constrict cerebral blood vessels, and enhance the effect of the first two drugs in relieving headaches.

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It is a central nervous system stimulant that can excite the cerebral cortex, increase sensitivity to the outside world, constrict cerebral blood vessels, and enhance the effect of the first two drugs in relieving headaches.

30mg 0
Chlorphenamine maleate

It has a strong histamine H1 receptor blocking effect, can alleviate other respiratory symptoms caused by allergies, and also has a mild inhibitory effect on the central nervous system.

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It has a strong histamine H1 receptor blocking effect, can alleviate other respiratory symptoms caused by allergies, and also has a mild inhibitory effect on the central nervous system.

2mg 113-92-8 28
Children's compound sulfamethoxazole tablets
This product is a compound preparation, each tablet contains the active ingredients 0.4g of sulfamethoxazole and 0.08g of trimethoprim.
Name Description Content CAS NO. Registered Holders
Sulfamethoxazole

After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

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After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

0.4g 723-46-6 33
Trimethoprim

After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

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After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

0.08g 738-70-5 44
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