-
Founded in:
1997-03-26 -
Country:
China -
Address:
No. 1, Minxie Road, Gulou District, Kaifeng City -
Tax NO.:
91410200706774630U -
Registered Funds:
33.56 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Angelicae Sinensis Radix |
|
0 | ||
| Radix astragali preparata |
|
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| REHMANNIAE RADIX PRAEPARATA |
|
0 | ||
| Cornus officinalis (processed) |
|
0 | ||
| MOUTAN CORTEX |
|
0 | ||
| Wild Yam P.E Diosgenine 7%-16% |
|
0 | ||
| Poria |
|
0 | ||
| ALISMATIS RHIZOMA |
|
0 | ||
| Yellow wine |
|
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| LONICERAE JAPONICAE FLOS |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| Forsythiae Fructus |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| PEPPERMINT |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| Schizonepeta |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| Semen sojae praeparatum |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| Burdock seeds (fried) |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| Platycodonis Radix |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| LOPHATHERI HERBA |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 | ||
| DGL |
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic
More
Antipyretic, antibacterial, antiviral, anti-inflammatory, analgesic |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Medicated Leaven Extract |
|
0 | ||
| Fructus oryzae germinatus |
|
0 | ||
| Maltitol |
|
585-88-6 | 6 | |
| Hawthorn |
|
0 | ||
| Atractylodis Macrocephalae Rhizoma |
|
0 | ||
| AURANTII FRUCTUS |
|
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Dogbane Leaf |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
0 | ||
| Chrysanthelandioum |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
0 | ||
| STEPHANIAE TETRANDRAE RADIX |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
0 | ||
| Magnesium trisilicate |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
14987-04-3 | 11 | |
| Dihydralazine sulphate |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
7327-87-9 | 9 | |
| Hydrochlorothiazide |
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia
More
Can significantly lower blood pressure; can slow heart rate; fight arrhythmia |
58-93-5 | 54 | |
| Promethazine hydrochloride |
Reduces spontaneous activity in mice and has a synergistic effect with sodium pentobarbital
More
Reduces spontaneous activity in mice and has a synergistic effect with sodium pentobarbital |
58-33-3 | 29 | |
| Chlordiazepoxide |
Reduces spontaneous activity in mice and has a synergistic effect with sodium pentobarbital
More
Reduces spontaneous activity in mice and has a synergistic effect with sodium pentobarbital |
0 | ||
| Thiamine chloride |
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex.
More
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex. |
1gg | 59-43-8 | 9 |
| Vitamin B6 |
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex.
More
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex. |
8059-24-3 | 13 | |
| Calcium D-Pantothenate |
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex.
More
This product was administered orally to experimental dogs with renal hypertension at a dose of 0.2g/kg, which significantly reduced blood pressure from 190/142 to 153/98mmHg 2 hours after oral administration. This product was administered orally to dogs and cats at 0.2 and 0.4g/kg, which slowed the heart rate 20 minutes later and lasted for 5 hours. This product was administered orally to rats at 0.3 and 0.6g/kg, which significantly counteracted arrhythmias caused by aconitine, calcium chloride and coronary artery ligation, and its anti-arrhythmic mechanism may be related to the effect on calcium ion influx. This product was administered orally to mice at 0.6 and 1.2g/kg, which reduced spontaneous activity in mice, and had a synergistic effect with sodium pentobarbital, causing the mice to lose their righting reflex. |
137-08-6 | 8 |