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Tianjin Pacific Pharmaceutical Co., Ltd.
  • Founded in:

    1994-08-08
  • Country:

    China China
  • Address:

    Economic Development Zone, Xiqing District, Tianjin
  • Tax NO.:

    91120111600584134N
  • Registered Funds:

    133.19 million yuan
  • Website:

  • Email:

Related Drugs
Dibazole Tablets
Main ingredients: The chemical name of this product is: 2-benzylbenzimidazole hydrochloride. Molecular formula: C14H12N2·HCl Molecular weight: 244.72
Name Description Content CAS NO. Registered Holders
2-Benzylbenzimidazole hydrochloride

It has a direct relaxing effect on vascular smooth muscle, reducing peripheral resistance and lowering blood pressure. It has an antispasmodic effect on gastrointestinal smooth muscle.

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It has a direct relaxing effect on vascular smooth muscle, reducing peripheral resistance and lowering blood pressure. It has an antispasmodic effect on gastrointestinal smooth muscle.

0
Dibazole Tablets
Main ingredients: The chemical name of this product is: 2-benzylbenzimidazole hydrochloride. Molecular formula: C14H12N2·HCl Molecular weight: 244.72
Name Description Content CAS NO. Registered Holders
2-Benzylbenzimidazole hydrochloride

It has a direct relaxing effect on vascular smooth muscle, reducing peripheral resistance and lowering blood pressure. It has an antispasmodic effect on gastrointestinal smooth muscle.

More

It has a direct relaxing effect on vascular smooth muscle, reducing peripheral resistance and lowering blood pressure. It has an antispasmodic effect on gastrointestinal smooth muscle.

0
Ribavirin Tablets
Ribavirin
Name Description Content CAS NO. Registered Holders
Ribavirin

Broad-spectrum antiviral drug. It has the effect of inhibiting the growth of multiple viruses such as respiratory syncytial virus, influenza virus, hepatitis A virus, adenovirus, etc. in vitro. After entering the virus-infected cells, the drug is rapidly phosphorylated, and its product acts as a competitive inhibitor of viral synthase, inhibiting inosine monophosphate dehydrogenase, influenza virus RNA polymerase and mRNA guanosine transferase, thereby causing a decrease in intracellular guanosine triphosphate, impairing viral RNA and protein synthesis, and inhibiting viral replication and transmission. It may also have an immune effect and neutralizing antibody effect on respiratory syncytial virus.

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Broad-spectrum antiviral drug. It has the effect of inhibiting the growth of multiple viruses such as respiratory syncytial virus, influenza virus, hepatitis A virus, adenovirus, etc. in vitro. After entering the virus-infected cells, the drug is rapidly phosphorylated, and its product acts as a competitive inhibitor of viral synthase, inhibiting inosine monophosphate dehydrogenase, influenza virus RNA polymerase and mRNA guanosine transferase, thereby causing a decrease in intracellular guanosine triphosphate, impairing viral RNA and protein synthesis, and inhibiting viral replication and transmission. It may also have an immune effect and neutralizing antibody effect on respiratory syncytial virus.

36791-04-5 33
Compound dexamethasone acetate cream
This product is a compound preparation, each gram contains 0.75 mg of dexamethasone acetate, 10 mg of camphor, and 10 mg of menthol.
Name Description Content CAS NO. Registered Holders
Dexamethasone-17-acetate

Adrenal cortical hormones have anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

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Adrenal cortical hormones have anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

0.75mg 1177-87-3 13
D-CAMPHOR

Adrenal cortex hormone drugs. This product has anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

More

Adrenal cortex hormone drugs. This product has anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

10mg 464-49-3 2
DL-Menthol

Adrenal cortex hormone drugs. This product has anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

More

Adrenal cortex hormone drugs. This product has anti-inflammatory and anti-allergic effects, can inhibit the proliferation of connective tissue, reduce the permeability of capillary walls and cell membranes, reduce inflammatory exudate, and inhibit the formation and release of histamine and other toxic substances.

10mg 89-78-1 8
Chenodeoxycholic acid capsules
Main ingredients and their chemical names: Chenodeoxycholic acid, chemical name 3alpha;, 7alpha;-dihydroxy-5beta;-cholanic acid
Name Description Content CAS NO. Registered Holders
Chenodeoxycholic acid

The main function of CDCA is to reduce the saturation of cholesterol in bile. After taking CDCA for most patients (when CDCA accounts for 70% of bile salts in bile), lipids return to the micelle state and cholesterol is in an unsaturated state, thereby dissolving and falling off the cholesterol in the stones. Large doses of CDCA (10-15 mg/kg per day) can inhibit the synthesis of cholesterol and increase the secretion of bile in patients with cholelithiasis, but the secretion of bile salts and phospholipids remains unchanged.

More

The main function of CDCA is to reduce the saturation of cholesterol in bile. After taking CDCA for most patients (when CDCA accounts for 70% of bile salts in bile), lipids return to the micelle state and cholesterol is in an unsaturated state, thereby dissolving and falling off the cholesterol in the stones. Large doses of CDCA (10-15 mg/kg per day) can inhibit the synthesis of cholesterol and increase the secretion of bile in patients with cholelithiasis, but the secretion of bile salts and phospholipids remains unchanged.

474-25-9 10
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