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Founded in:
2001-08-09 -
Country:
China -
Address:
No. 113, Lianhua West Road, Shilou Town, Panyu District, Guangzhou -
Tax NO.:
914401137315771107 -
Registered Funds:
HK$270 million -
Website:
-
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Gentamicin sulfate |
This product is an aminoglycoside antibiotic that has good antibacterial effects on various Gram-negative and Gram-positive bacteria. The mechanism of action is to bind to the 30S subunit of the bacterial ribosome and inhibit the synthesis of bacterial proteins. In recent years, the number of Gram-negative bacteria resistant to gentamicin has increased significantly.
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This product is an aminoglycoside antibiotic that has good antibacterial effects on various Gram-negative and Gram-positive bacteria. The mechanism of action is to bind to the 30S subunit of the bacterial ribosome and inhibit the synthesis of bacterial proteins. In recent years, the number of Gram-negative bacteria resistant to gentamicin has increased significantly. |
1405-41-0 | 29 |
| 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 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 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 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 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 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 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 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 be secreted into breast milk. |
0.08g | 738-70-5 | 44 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Rotundine |
A non-narcotic analgesic with analgesic, sedative, hypnotic and tranquilizer effects; the analgesic effect is stronger than that of general antipyretic analgesics, with the analgesic effect appearing 10 minutes after taking the medicine and lasting for 2-5 hours; it has a good analgesic effect on dull pain caused by the gastrointestinal system, but has a poor effect on severe pain such as trauma; it is also effective for menstrual pain, and is more suitable for insomnia, especially insomnia caused by pain, with no aftereffects after waking up.
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A non-narcotic analgesic with analgesic, sedative, hypnotic and tranquilizer effects; the analgesic effect is stronger than that of general antipyretic analgesics, with the analgesic effect appearing 10 minutes after taking the medicine and lasting for 2-5 hours; it has a good analgesic effect on dull pain caused by the gastrointestinal system, but has a poor effect on severe pain such as trauma; it is also effective for menstrual pain, and is more suitable for insomnia, especially insomnia caused by pain, with no aftereffects after waking up. |
93.0%～107.0%C21H25NO4 nominal amount | 10097-84-4 | 15 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Bromhexine hydrochloride |
This product acts directly on the bronchial glands, releasing the lysosomes of mucus-secreting cells, thereby depolymerizing the mucopolysaccharides in the mucus and reducing the viscosity of the mucus; it can also cause the respiratory tract to secrete low-viscosity small-molecule mucins, making the sputum thinner and easier to cough up.
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This product acts directly on the bronchial glands, releasing the lysosomes of mucus-secreting cells, thereby depolymerizing the mucopolysaccharides in the mucus and reducing the viscosity of the mucus; it can also cause the respiratory tract to secrete low-viscosity small-molecule mucins, making the sputum thinner and easier to cough up. |
8mg | 611-75-6 | 26 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Tetracycline |
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Extract from the above information |
60-54-8 | 25 |