-
Founded in:
1989-08-29 -
Country:
China -
Address:
No. 22, Minhang South Road, Xiaodian District, Taiyuan City -
Tax NO.:
911401051100866506 -
Registered Funds:
11.56938626 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Aluminum hydroxide |
Antacids, which neutralize stomach acid and protect the ulcer surface
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Antacids, which neutralize stomach acid and protect the ulcer surface |
140mg | 21645-51-2 | 14 |
| Vitamin U (iodomethylmethionine) |
Promote granulation development and mucosal regeneration
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Promote granulation development and mucosal regeneration |
50mg | 0 | |
| Atropa Belladonnal |
Inhibit glandular secretion and relieve pain caused by smooth spasm
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Inhibit glandular secretion and relieve pain caused by smooth spasm |
10mg | 0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Protionamide |
This product is a derivative of isonicotinic acid. Its mechanism of action is unknown. It may have an inhibitory effect on peptide synthesis. The effect of this product on Mycobacterium tuberculosis depends on the drug concentration at the infected site. It only has an antibacterial effect at low concentrations and a bactericidal effect at high concentrations. It inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis. This product has partial cross-resistance with ethionamide.
More
This product is a derivative of isonicotinic acid. Its mechanism of action is unknown. It may have an inhibitory effect on peptide synthesis. The effect of this product on Mycobacterium tuberculosis depends on the drug concentration at the infected site. It only has an antibacterial effect at low concentrations and a bactericidal effect at high concentrations. It inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis. This product has partial cross-resistance with ethionamide. |
14222-60-7 | 4 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Cyperus rotundus (made with vinegar) |
|
0 | ||
| DGL |
|
0 | ||
| Corydalis yanhusuo (fried with vinegar) |
|
0 | ||
| Nepeta tenuifolia carbon, flavonoids, saponins, polysaccharides, polyphenols, alkaloids, volatile oils |
|
0 | ||
| Poria |
|
0 | ||
| Magnolia |
|
0 | ||
| Curcuma zedoaria (fried with vinegar) |
|
0 | ||
| CURCUMAE RADIX |
|
0 | ||
| Citri reticulatae pericarpium |
|
0 | ||
| Bupleurum (roasted with wine) |
|
0 | ||
| Argy Wormwood Leaf |
|
0 | ||
| Linderae Radix |
|
0 | ||
| Angelicae Sinensis Radix |
|
0 | ||
| Aucklandiae Radix |
|
0 | ||
| MOUTAN CORTEX |
|
0 | ||
| CARTHAMI FLOS |
|
0 | ||
| PERSICAE SEMEN |
|
0 | ||
| dogwood |
|
0 | ||
| donkey-hide gelatin |
|
0 | ||
| REHMANNIAE RADIX PRAEPARATA |
|
0 | ||
| PAEONIAE RADIX ALBA |
|
0 | ||
| Astragali Radix |
|
0 | ||
| Salvia Root P.E Tanshinone IIA 20% |
|
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Captopril |
Inhibit the activity of angiotensin converting enzyme, reduce the level of angiotensin II, reduce the secretion of aldosterone, dilate arteries and veins, achieve a hypotensive effect and reduce the preload and afterload of the heart to improve heart function
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Inhibit the activity of angiotensin converting enzyme, reduce the level of angiotensin II, reduce the secretion of aldosterone, dilate arteries and veins, achieve a hypotensive effect and reduce the preload and afterload of the heart to improve heart function |
62571-86-2 | 28 | |
| Hydrochlorothiazide |
Increase the excretion of sodium chloride by the kidneys to play a diuretic role, reduce blood volume, and exert a hypotensive effect
More
Increase the excretion of sodium chloride by the kidneys to play a diuretic role, reduce blood volume, and exert a hypotensive effect |
58-93-5 | 54 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| 1-(2,6-Dichlorophenyl)-2-indolinone |
Diclofenac is a non-steroidal anti-inflammatory analgesic derived from phenylacetic acid. Its mechanism of action is to inhibit the activity of cyclooxygenase, thereby blocking the conversion of arachidonic acid into prostaglandins. At the same time, it can also promote the combination of arachidonic acid and triglycerides (triacylglycerols), reduce the concentration of free arachidonic acid in cells, and indirectly inhibit the synthesis of leukotrienes. Diclofenac is a stronger non-steroidal anti-inflammatory drug. Its inhibitory effect on prostaglandin synthesis is stronger than that of aspirin and indomethacin.
More
Diclofenac is a non-steroidal anti-inflammatory analgesic derived from phenylacetic acid. Its mechanism of action is to inhibit the activity of cyclooxygenase, thereby blocking the conversion of arachidonic acid into prostaglandins. At the same time, it can also promote the combination of arachidonic acid and triglycerides (triacylglycerols), reduce the concentration of free arachidonic acid in cells, and indirectly inhibit the synthesis of leukotrienes. Diclofenac is a stronger non-steroidal anti-inflammatory drug. Its inhibitory effect on prostaglandin synthesis is stronger than that of aspirin and indomethacin. |
15307-86-5 | 4 |