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

    2009-03-10
  • Country:

    China China
  • Address:

    No. 685, Xinji Road, Qingpu District, Shanghai
  • Tax NO.:

    91310105685497805C
  • Registered Funds:

    93.641789 yuan
  • Website:

  • Email:

Related Drugs
Molsomal tablets
Name Description Content CAS NO. Registered Holders
Molsidomine

Unspecified

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Unspecified

25717-80-0 4
Chondroitin Sulfate Sodium Tablets
It is an acidic mucopolysaccharide extracted from the cartilage tissue of the pig's larynx, nasal bone, trachea, etc. The hexose amino content of this product is calculated as glucosamine (C6H13O5N), which shall not be less than 24.0% of the labeled amount of chondroitin sulfate.
Name Description Content CAS NO. Registered Holders
Chondroitin 4-sulfate

It can remove lipids and lipoproteins from the blood and prevent and treat atherosclerosis; it can effectively prevent and treat coronary heart disease, resist atherosclerosis and the formation of atherosclerotic plaques; it can increase the biosynthesis of cellular mRNA and DNA and promote cell metabolism; it has a mild anticoagulant effect (each 1 mg of chondroitin sulfate A is equivalent to the anticoagulant activity of 0.45 U of heparin); it has anti-inflammatory, accelerates wound healing and anti-tumor effects.

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It can remove lipids and lipoproteins from the blood and prevent and treat atherosclerosis; it can effectively prevent and treat coronary heart disease, resist atherosclerosis and the formation of atherosclerotic plaques; it can increase the biosynthesis of cellular mRNA and DNA and promote cell metabolism; it has a mild anticoagulant effect (each 1 mg of chondroitin sulfate A is equivalent to the anticoagulant activity of 0.45 U of heparin); it has anti-inflammatory, accelerates wound healing and anti-tumor effects.

Not less than 24.0% of the labeled amountGlucosamine (C6H13O5N) 9007-28-7 2
Dragon Tiger Pill
Menthol, borneol, cloves, amomum villosum, star anise, cinnamon, pepper, costus root, dried ginger, catechu, licorice, glutinous rice flour, sodium benzoate, red iron oxide, dextrin, talc, methyl silicone oil, graphite powder, ethanol.
Name Description Content CAS NO. Registered Holders
Borneol

507-70-0 1
DGL

0
CATECHU

0
Zingiberis Rhizoma

0
Aucklandiae Radix

0
Black Pepper Oil

8006-82-4 0
Cassia Aurantium P.E Catechins 8% HPLC

0
Anise oil

8007-70-3 10
Amomum villosum Lour

0
Clove oil

8000-34-8 4
DL-Menthol

89-78-1 8
Glutinous Rice Powder Flavor

0
Sodium benzoate

532-32-1 23
Ferric oxide

1309-37-1 7
Dextrin

9004-53-9 49
Talc

14807-96-6 26
SILICONE OV-101

0
Graphite

7782-42-5 0
Ethanol

64-17-5 91
Freeze-dried royal jelly capsules
Royal jelly, micro powder silica gel.
Name Description Content CAS NO. Registered Holders
Royal Jelly

8031-67-2 0
Microsilica gel

0
Lisinopril Tablets
The main ingredient of this product is: lisinopril.
Name Description Content CAS NO. Registered Holders
Lisinopril Dihydrate

This product is a third-generation angiotensin converting enzyme inhibitor, which can inhibit the activity of angiotensin converting enzyme, reduce the concentration of angiotensin II and aldosterone, increase plasma renin activity, lead to peripheral vasodilation and decreased vascular resistance, and thus produce a hypotensive effect. The hypotensive effect occurs within about 2 hours after oral administration, and the maximum hypotensive effect occurs about 4 to 6 hours after oral administration, which is consistent with the peak time of blood drug concentration (tmax). The hypotensive effect lasts for 24 hours, and there will be no blood pressure rebound after stopping the drug, and there is no significant change in heart rate after taking the drug.

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This product is a third-generation angiotensin converting enzyme inhibitor, which can inhibit the activity of angiotensin converting enzyme, reduce the concentration of angiotensin II and aldosterone, increase plasma renin activity, lead to peripheral vasodilation and decreased vascular resistance, and thus produce a hypotensive effect. The hypotensive effect occurs within about 2 hours after oral administration, and the maximum hypotensive effect occurs about 4 to 6 hours after oral administration, which is consistent with the peak time of blood drug concentration (tmax). The hypotensive effect lasts for 24 hours, and there will be no blood pressure rebound after stopping the drug, and there is no significant change in heart rate after taking the drug.

83915-83-7 21
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