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Shanghai Yishengyuan Pharmaceutical Co., Ltd.
  • Founded in:

    2001-06-26
  • Country:

    China China
  • Address:

    No. 139, Jianhao Road, Pudong New Area
  • Tax NO.:

    913101157033635104
  • Registered Funds:

    111.1106 million yuan
  • Email:

Related Drugs
Levofloxacin Hydrochloride Tablets
Levofloxacin hydrochloride.
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Levofloxacin hydrochloride

It achieves antibacterial effect by inhibiting the activity of bacterial DNA gyrase (bacterial topoisomerase II) and hindering bacterial replication. It has good antibacterial effect on most Enterobacteriaceae, some Gram-positive bacteria and Legionella, mycoplasma, Chlamydia, etc., but has poor effect on anaerobic bacteria and enterococci.

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It achieves antibacterial effect by inhibiting the activity of bacterial DNA gyrase (bacterial topoisomerase II) and hindering bacterial replication. It has good antibacterial effect on most Enterobacteriaceae, some Gram-positive bacteria and Legionella, mycoplasma, Chlamydia, etc., but has poor effect on anaerobic bacteria and enterococci.

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Artemisia argyi dampness spray
Artemisia annua, Angelica dahurica, Cynanchum wilfordii, Olea europaea, Cassia twig, camphor, menthol, Belladonna fluid extract, Curcuma zedoaria.
Name Description Content CAS NO. Registered Holders
Artemisia scoparia

0
Angelicae Dahuricae Radix

0
CYNANCHI PANICULATI RADIX ET RHIZOMA

0
RADIX TINOSPORAE

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Cmnamomi Mmulus

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D-CAMPHOR

464-49-3 1
DL-Menthol

89-78-1 8
Extract Belladonna soft liquid and powder

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Zedoary turmeric

0
Benserazide hydrochloride
Name Description Content CAS NO. Registered Holders
Benserazide hydrochloride

No specific description provided

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No specific description provided

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Oxaprozin Enteric-coated Capsules
The main ingredient of this product is oxaprozin, whose chemical name is 4,5-diphenyloxazole-2-propionic acid.
Name Description Content CAS NO. Registered Holders
Oxaprozin

This product belongs to the propionic acid class of nonsteroidal anti-inflammatory drugs, with anti-inflammatory, analgesic and antipyretic effects. It reduces the synthesis of inflammatory mediators prostaglandins by inhibiting cyclooxygenase, so that the swelling and pain of local tissues caused by prostaglandins can be controlled. The anti-inflammatory effect of this product is stronger than that of ibuprofen, and the analgesic effect is better than that of ibuprofen, phenylbutazone and aspirin, while the gastric mucosal damage effect is lower than that of aspirin and phenylbutazone. It causes slight damage to the digestive tract and the drug effect is long-lasting. This drug has a central muscle relaxant effect.

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This product belongs to the propionic acid class of nonsteroidal anti-inflammatory drugs, with anti-inflammatory, analgesic and antipyretic effects. It reduces the synthesis of inflammatory mediators prostaglandins by inhibiting cyclooxygenase, so that the swelling and pain of local tissues caused by prostaglandins can be controlled. The anti-inflammatory effect of this product is stronger than that of ibuprofen, and the analgesic effect is better than that of ibuprofen, phenylbutazone and aspirin, while the gastric mucosal damage effect is lower than that of aspirin and phenylbutazone. It causes slight damage to the digestive tract and the drug effect is long-lasting. This drug has a central muscle relaxant effect.

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Sulpiride Tablets
The main ingredient of this product is Sulpiride, and its chemical name is: N-[methyl-(1-ethyl-2-pyrrolidinyl)]-2-methoxy-5-aminosulfonyl)-benzamide.
Name Description Content CAS NO. Registered Holders
Sulpiride

This product belongs to the benzamide antipsychotic drug. Its characteristic action is to selectively block the dopamine (DA2) receptors of the mesolimbic system, with little effect on other neurotransmitter receptors, mild anticholinergic effect, and no obvious sedative and anti-excitement and agitation effects. This product also has strong antiemetic and gastric juice secretion inhibitory effects.

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This product belongs to the benzamide antipsychotic drug. Its characteristic action is to selectively block the dopamine (DA2) receptors of the mesolimbic system, with little effect on other neurotransmitter receptors, mild anticholinergic effect, and no obvious sedative and anti-excitement and agitation effects. This product also has strong antiemetic and gastric juice secretion inhibitory effects.

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