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Anhui Renhe Pharmaceutical Co., Ltd.

  • Founded in:

    1991-12-15
  • Country:

    China China
  • Address:

    No. 27 Xinyang Avenue, Fuyang Economic and Technological Development Zone
  • Tax NO.:

    913412007349648451
  • Registered Funds:

    16.8 million yuan
  • Website:

  • Email:

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Chlorphenamine yellow sensitive tablets
This product is a compound preparation, and its components per tablet are: diclofenac sodium 15 mg, artificial bezoar 15 mg, and chlorpheniramine maleate 2.5 mg.
Name Description Content CAS NO. Registered Holders
Diclofenac sodium

Inhibits cyclooxygenase activity, thereby blocking the conversion of arachidonic acid to prostaglandins; promotes the combination of arachidonic acid and triglycerides, reduces the concentration of free arachidonic acid in cells, and indirectly inhibits the synthesis of leukotrienes; the inhibitory effect on prostaglandin synthesis is stronger than aspirin and indomethacin, etc.

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Inhibits cyclooxygenase activity, thereby blocking the conversion of arachidonic acid to prostaglandins; promotes the combination of arachidonic acid and triglycerides, reduces the concentration of free arachidonic acid in cells, and indirectly inhibits the synthesis of leukotrienes; the inhibitory effect on prostaglandin synthesis is stronger than aspirin and indomethacin, etc.

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Atificial Cow-bezoar

Antipyretic, analgesic, sedative, anti-inflammatory

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Antipyretic, analgesic, sedative, anti-inflammatory

15mg 1002-00-2 2
Chlorphenamine maleate

It can counteract the allergic reaction of histamine by antagonizing H1 receptors, does not affect histamine metabolism, does not prevent the release of histamine in the body, and has M cholinergic receptor blocking and central inhibition effects

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It can counteract the allergic reaction of histamine by antagonizing H1 receptors, does not affect histamine metabolism, does not prevent the release of histamine in the body, and has M cholinergic receptor blocking and central inhibition effects

2.5mg 113-92-8 28
Ibuprofen tablets
Ibuprofen
Name Description Content CAS NO. Registered Holders
Ibuprofen

This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects.

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This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects.

15687-27-1 54
Xiaoyao Pills
Bupleurum, Chinese angelica, white peony root, Atractylodes macrocephala (fried), Poria, roasted licorice, and mint.
Name Description Content CAS NO. Registered Holders
Bupleurum

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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Angelicae Sinensis Radix

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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PAEONIAE RADIX ALBA

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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Atractylodes macrocephala (fried)

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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Poria

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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Licorice root flavonoids saponins polysaccharides polyphenols alkaloids volatile oils

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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PEPPERMINT

It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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It has antidepressant effects; it can lower blood pressure and dilate blood vessels

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Tripibutone Tablets
Tripibuton, chemical name: 3-(2,4,5-triethoxybenzoyl)propionic acid.
Name Description Content CAS NO. Registered Holders
Trepibutone

It selectively relaxes the ballistic smooth muscle and directly inhibits the sphincter of Oddi in the biliary tract, thereby relaxing the biliary sphincter and reducing the resistance to passage through the common bile duct and the duodenum. It also reduces the pressure inside the gallbladder and bile duct, promotes the discharge of bile and pancreatic juice, improves appetite, and eliminates abdominal distension. It has antispasmodic, analgesic and choleretic effects.

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It selectively relaxes the ballistic smooth muscle and directly inhibits the sphincter of Oddi in the biliary tract, thereby relaxing the biliary sphincter and reducing the resistance to passage through the common bile duct and the duodenum. It also reduces the pressure inside the gallbladder and bile duct, promotes the discharge of bile and pancreatic juice, improves appetite, and eliminates abdominal distension. It has antispasmodic, analgesic and choleretic effects.

41826-92-0 9
Erythromycin Enteric-coated Tablets
The main ingredient of this product is erythromycin
Name Description Content CAS NO. Registered Holders
Erythromycin

This product belongs to the macrolide antibiotics. It has antibacterial activity against Staphylococcus (except methicillin-resistant strains), all groups of streptococci and Gram-positive bacilli. Neisseria, Haemophilus influenzae, Bordetella pertussis, etc. are also sensitive to this product. This product also has antibacterial effects on various anaerobic bacteria except Bacteroides fragilis and Fusobacterium. It also has inhibitory effects on Legionella, Campylobacter fetus, certain spirochetes, Mycoplasma pneumoniae, Rickettsia and Chlamydia. This product is an antibacterial agent, but it also has a bactericidal effect on certain bacteria at high concentrations. It can penetrate the bacterial cell membrane and reversibly bind to the 50S subunit of the bacterial ribosome near the donor site ("P" site), blocking the transfer RNA (t-RNA) from binding to the "P" site, and also blocking the self-acceptor site ("A" site) of the polypeptide chain.

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This product belongs to the macrolide antibiotics. It has antibacterial activity against Staphylococcus (except methicillin-resistant strains), all groups of streptococci and Gram-positive bacilli. Neisseria, Haemophilus influenzae, Bordetella pertussis, etc. are also sensitive to this product. This product also has antibacterial effects on various anaerobic bacteria except Bacteroides fragilis and Fusobacterium. It also has inhibitory effects on Legionella, Campylobacter fetus, certain spirochetes, Mycoplasma pneumoniae, Rickettsia and Chlamydia. This product is an antibacterial agent, but it also has a bactericidal effect on certain bacteria at high concentrations. It can penetrate the bacterial cell membrane and reversibly bind to the 50S subunit of the bacterial ribosome near the donor site ("P" site), blocking the transfer RNA (t-RNA) from binding to the "P" site, and also blocking the self-acceptor site ("A" site) of the polypeptide chain.

114-07-8 43
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