Jinling Pharmaceutical Co., Ltd. Nanjing Jinling Pharmaceutical Factory
-
Founded in:
1996-09-16 -
Country:
China -
Address:
No. 58, Xingang Avenue, Nanjing Economic and Technological Development Zone -
Tax NO.:
9132019270413930XB -
Registered Funds:
- -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| 4-Methylumbelliferone |
It can relax the sphincter of Oddi, has strong antispasmodic and analgesic effects, and can also gently and continuously promote bile secretion, strengthen gallbladder contraction and antibacterial effects, has obvious choleretic effects, is conducive to the discharge of stones, and has a certain stone discharge effect on common bile duct stones. Some patients with elevated alanine aminotransferase will return to normal after taking the medicine as the inflammation is eliminated. This product has low toxicity, and the acute toxicity LD50 of mice is 5375mg/kg.
More
It can relax the sphincter of Oddi, has strong antispasmodic and analgesic effects, and can also gently and continuously promote bile secretion, strengthen gallbladder contraction and antibacterial effects, has obvious choleretic effects, is conducive to the discharge of stones, and has a certain stone discharge effect on common bile duct stones. Some patients with elevated alanine aminotransferase will return to normal after taking the medicine as the inflammation is eliminated. This product has low toxicity, and the acute toxicity LD50 of mice is 5375mg/kg. |
90-33-5 | 5 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Active ingredients extracted from licorice root |
Increase the "glycosamine" content of gastric mucosal cells, improve the defense of gastric mucosa, prolong the life of gastric epithelial cells, and accelerate the healing of ulcers
More
Increase the "glycosamine" content of gastric mucosal cells, improve the defense of gastric mucosa, prolong the life of gastric epithelial cells, and accelerate the healing of ulcers |
0 | ||
| ZINC |
Promote mucosal regeneration and accelerate ulcer healing
More
Promote mucosal regeneration and accelerate ulcer healing |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Nicardipine hydrochloride |
1. Calcium channel blocker, inhibits transmembrane calcium ion influx of myocardial and vascular smooth muscle without changing blood calcium concentration; 2. Has high vascular selectivity and dilates coronary vascular smooth muscle; 3. Can increase exercise tolerance of patients with chronic stable angina pectoris and reduce the frequency of angina attacks; 4. Reduces peripheral vascular resistance and blood pressure, can reduce systolic and diastolic blood pressure in patients with mild and moderate hypertension, but does not change the circadian rhythm of blood pressure; 5. Increases cardiac ejection fraction and cardiac output, with little change in left ventricular end-diastolic pressure; 6. Can temporarily increase urinary sodium excretion; 7. Blocks slow calcium channels without affecting fast sodium channels; 8. Does not affect atrioventricular conduction.
More
1. Calcium channel blocker, inhibits transmembrane calcium ion influx of myocardial and vascular smooth muscle without changing blood calcium concentration; 2. Has high vascular selectivity and dilates coronary vascular smooth muscle; 3. Can increase exercise tolerance of patients with chronic stable angina pectoris and reduce the frequency of angina attacks; 4. Reduces peripheral vascular resistance and blood pressure, can reduce systolic and diastolic blood pressure in patients with mild and moderate hypertension, but does not change the circadian rhythm of blood pressure; 5. Increases cardiac ejection fraction and cardiac output, with little change in left ventricular end-diastolic pressure; 6. Can temporarily increase urinary sodium excretion; 7. Blocks slow calcium channels without affecting fast sodium channels; 8. Does not affect atrioventricular conduction. |
54527-84-3 | 33 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Nefopam hydrochloride |
This product is a new type of non-narcotic analgesic, with mild antipyretic and muscle relaxant effects. Its chemical structure belongs to cyclized o-methylbenzylamine. Therefore, it does not have the characteristics of non-steroidal anti-inflammatory drugs, nor is it an opioid receptor agonist. It is effective for moderate and severe pain. An intramuscular injection of 20 mg of this product is equivalent to the effect of 12 mg of morphine. It has a mild respiratory depressant effect. It has no depressant effect on the circulatory system. There is no tolerance and dependence.
More
This product is a new type of non-narcotic analgesic, with mild antipyretic and muscle relaxant effects. Its chemical structure belongs to cyclized o-methylbenzylamine. Therefore, it does not have the characteristics of non-steroidal anti-inflammatory drugs, nor is it an opioid receptor agonist. It is effective for moderate and severe pain. An intramuscular injection of 20 mg of this product is equivalent to the effect of 12 mg of morphine. It has a mild respiratory depressant effect. It has no depressant effect on the circulatory system. There is no tolerance and dependence. |
23327-57-3 | 12 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Piracetam |
It is a similar substance of aminobutyric acid, which can activate, protect and repair brain cells, improve brain hypoxia, activate brain cells, increase the ATP/ADP ratio in the brain, promote the absorption of amino acids and phospholipids, protein synthesis, glucose utilization and energy storage, promote brain metabolism, increase cerebral blood flow. It can accelerate the speed of information transmission between the cerebral hemispheres through the corpus callosum, and improve the ability of learning, memory and thinking activities.
More
It is a similar substance of aminobutyric acid, which can activate, protect and repair brain cells, improve brain hypoxia, activate brain cells, increase the ATP/ADP ratio in the brain, promote the absorption of amino acids and phospholipids, protein synthesis, glucose utilization and energy storage, promote brain metabolism, increase cerebral blood flow. It can accelerate the speed of information transmission between the cerebral hemispheres through the corpus callosum, and improve the ability of learning, memory and thinking activities. |
0.114g | 7491-74-9 | 25 |
| Choline bitartrate |
It is a similar substance of aminobutyric acid, which can activate, protect and repair brain cells, improve brain hypoxia, activate brain cells, increase the ATP/ADP ratio in the brain, promote the absorption of amino acids and phospholipids, protein synthesis, glucose utilization and energy storage, promote brain metabolism, increase cerebral blood flow. It can accelerate the speed of information transmission between the cerebral hemispheres through the corpus callosum, and improve the ability of learning, memory and thinking activities.
More
It is a similar substance of aminobutyric acid, which can activate, protect and repair brain cells, improve brain hypoxia, activate brain cells, increase the ATP/ADP ratio in the brain, promote the absorption of amino acids and phospholipids, protein synthesis, glucose utilization and energy storage, promote brain metabolism, increase cerebral blood flow. It can accelerate the speed of information transmission between the cerebral hemispheres through the corpus callosum, and improve the ability of learning, memory and thinking activities. |
0.286g | 87-67-2 | 4 |