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Jiangsu Yunyang Group Pharmaceutical Co., Ltd.
  • Founded in:

    2003-07-17
  • Country:

    China China
  • Address:

    No. 18, Shunkang Road, Danyang Economic Development Zone, Jiangsu
  • Tax NO.:

    91321181752709469X
  • Registered Funds:

    100 million yuan
  • Website:

  • Email:

Related Drugs
Clonidine Hydrochloride
Name Description Content CAS NO. Registered Holders
Clonidine hydrochloride

Extract from the above information

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Extract from the above information

4205-91-8 23
Clonidine Hydrochloride Tablets
The main ingredient of this product is clonidine hydrochloride.
Name Description Content CAS NO. Registered Holders
Clonidine hydrochloride

1. Clonidine is an alpha receptor agonist. 2. It stimulates the alpha 2 receptors of the central postsynaptic membrane of the hypothalamus and medulla oblongata, reduces the outflow of central sympathetic nerve impulses, and inhibits peripheral sympathetic nerve activity; it stimulates the alpha 2 receptors of the presynaptic membrane of peripheral sympathetic nerves, reduces the release of norepinephrine, reduces peripheral vascular and renal vascular resistance, slows heart rate, and lowers blood pressure. 3. It moderately reduces cardiac output when lying without changing peripheral vascular resistance, and slightly reduces cardiac output and peripheral vascular resistance when tilted. 4. After long-term treatment, cardiac output tends to normal, but peripheral vascular resistance continues to decrease. 5. It reduces plasma renin activity and aldosterone and catecholamine secretion. 6. Acute use stimulates the release of growth hormone, but long-term use does not cause a continuous increase in growth hormone levels. 7. It can be used to treat migraine, dysmenorrhea, and menopausal hot flashes, which may work by stabilizing peripheral blood vessels, or by inhibiting the activity of alpha receptors in the brain to quit opioid addiction.

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1. Clonidine is an alpha receptor agonist. 2. It stimulates the alpha 2 receptors of the central postsynaptic membrane of the hypothalamus and medulla oblongata, reduces the outflow of central sympathetic nerve impulses, and inhibits peripheral sympathetic nerve activity; it stimulates the alpha 2 receptors of the presynaptic membrane of peripheral sympathetic nerves, reduces the release of norepinephrine, reduces peripheral vascular and renal vascular resistance, slows heart rate, and lowers blood pressure. 3. It moderately reduces cardiac output when lying without changing peripheral vascular resistance, and slightly reduces cardiac output and peripheral vascular resistance when tilted. 4. After long-term treatment, cardiac output tends to normal, but peripheral vascular resistance continues to decrease. 5. It reduces plasma renin activity and aldosterone and catecholamine secretion. 6. Acute use stimulates the release of growth hormone, but long-term use does not cause a continuous increase in growth hormone levels. 7. It can be used to treat migraine, dysmenorrhea, and menopausal hot flashes, which may work by stabilizing peripheral blood vessels, or by inhibiting the activity of alpha receptors in the brain to quit opioid addiction.

4205-91-8 23
Compound Radix Codonopsis pilosulae tincture
Tujingpi tincture %ml benzoic acid, salicylic acid,
Name Description Content CAS NO. Registered Holders
Compound soil

0
Benzoic acid

65-85-0 15
Salicylic acid

69-72-7 10
Compound salicylic acid solution
This product is a compound preparation, each milliliter contains 80 mg of salicylic acid, 20 mg each of phenol and resorcinol, and 0.02 ml of methyl salicylate.
Name Description Content CAS NO. Registered Holders
Salicylic acid

Analgesic, keratolytic and antifungal effects

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Analgesic, keratolytic and antifungal effects

80mg 69-72-7 10
Phenol

Antibacterial effect

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Antibacterial effect

20mg 108-95-2 14
Resorcinol

Antibacterial effect

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Antibacterial effect

20mg 108-46-3 8
Methyl salicylate

Anti-inflammatory, antipruritic, anti-swelling and analgesic effects

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Anti-inflammatory, antipruritic, anti-swelling and analgesic effects

0.02ml 119-36-8 19
Ketotifen Fumarate Tablets
Ketotifen Fumarate
Name Description Content CAS NO. Registered Holders
Ketotifen fumarate

It has both histamine H1 receptor antagonism and the effect of inhibiting the release of allergic reaction mediators. It not only has a strong anti-allergic effect, but also has a longer duration of efficacy. Therefore, it is more effective in preventing various bronchial asthma attacks and exogenous asthma than endogenous asthma.

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It has both histamine H1 receptor antagonism and the effect of inhibiting the release of allergic reaction mediators. It not only has a strong anti-allergic effect, but also has a longer duration of efficacy. Therefore, it is more effective in preventing various bronchial asthma attacks and exogenous asthma than endogenous asthma.

34580-14-8 13
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