On ECHEMI
Home > Drugs > Tangshan Likang Pharmaceutical Co., Ltd.
Tangshan Likang Pharmaceutical Co., Ltd.
  • Founded in:

    1999-12-22
  • Country:

    China China
  • Address:

    Tangshan Guye District Linxi Hexilixi
  • Tax NO.:

    9113020072161079XW
  • Registered Funds:

    12.9 million yuan
  • Email:

Related Drugs
Aminocaine and Huangmin Tablets
This product is a compound preparation. Each tablet contains 250 mg of acetaminophen, 15 mg of caffeine, 1 mg of chlorpheniramine maleate, and 10 mg of artificial bezoar.
Name Description Content CAS NO. Registered Holders
Acetaminophen

It can inhibit the synthesis of prostaglandins and has antipyretic and analgesic effects

More

It can inhibit the synthesis of prostaglandins and has antipyretic and analgesic effects

250mg 103-90-2 68
Caffeine

It is a central nervous system stimulant that can enhance the antipyretic and analgesic effects of acetaminophen and reduce central nervous system inhibitory effects such as drowsiness and dizziness caused by other drugs.

More

It is a central nervous system stimulant that can enhance the antipyretic and analgesic effects of acetaminophen and reduce central nervous system inhibitory effects such as drowsiness and dizziness caused by other drugs.

15mg 0
Chlorphenamine maleate

It is an antihistamine that can relieve runny nose, nasal congestion, and sneezing symptoms.

More

It is an antihistamine that can relieve runny nose, nasal congestion, and sneezing symptoms.

1mg 113-92-8 28
Atificial Cow-bezoar

It has antipyretic and sedative effects

More

It has antipyretic and sedative effects

10mg 1002-00-2 2
Cephalexin Tablets
The main ingredient of this product is cephalexin, and its chemical name is (6R,7R)-3-methyl-7-[(R)-2-amino-2-phenylacetylamino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid monohydrate.
Name Description Content CAS NO. Registered Holders
Cephalexin

Cephalexin is a first-generation cephalosporin with an antibacterial spectrum similar to that of cephalothin, but its antibacterial activity is poorer than that of the latter. Except for Enterococcus and methicillin-resistant Staphylococci, most strains of Streptococcus pneumoniae, hemolytic Streptococcus, and Staphylococcus aureus that produces or does not produce penicillinase are sensitive to this product. This product has a good antibacterial effect on Neisseria, but Haemophilus influenzae is less sensitive to this product; this product has a certain antibacterial effect on some Escherichia coli, Proteus mirabilis, Salmonella and Shigella. The remaining Enterobacteriaceae, Acinetobacter, Pseudomonas aeruginosa, and Bacteroides fragilis are resistant to this product. Fusobacterium and Veillonella are generally sensitive to this product, and anaerobic Gram-positive cocci are moderately sensitive to this product.

More

Cephalexin is a first-generation cephalosporin with an antibacterial spectrum similar to that of cephalothin, but its antibacterial activity is poorer than that of the latter. Except for Enterococcus and methicillin-resistant Staphylococci, most strains of Streptococcus pneumoniae, hemolytic Streptococcus, and Staphylococcus aureus that produces or does not produce penicillinase are sensitive to this product. This product has a good antibacterial effect on Neisseria, but Haemophilus influenzae is less sensitive to this product; this product has a certain antibacterial effect on some Escherichia coli, Proteus mirabilis, Salmonella and Shigella. The remaining Enterobacteriaceae, Acinetobacter, Pseudomonas aeruginosa, and Bacteroides fragilis are resistant to this product. Fusobacterium and Veillonella are generally sensitive to this product, and anaerobic Gram-positive cocci are moderately sensitive to this product.

15686-71-2 33
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.

More

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
Flunarizine Hydrochloride Capsules
Flunarizine hydrochloride. Its chemical name is: (E)-1-[bis(4-fluorophenyl)methyl]-4-2(2-propenyl-3-phenyl)-piperazine dihydrochloride.
Name Description Content CAS NO. Registered Holders
Flunarizine dihydrochloride

This product is a calcium channel blocker. It can prevent cell damage caused by pathological calcium overload in cells due to ischemia and other reasons. It has the following effects: 1. Relieve vasospasm, especially for the basilar artery and internal carotid artery; 2. Vestibular inhibition, which can increase blood flow in the cochlear arterioles and improve vestibular organ circulation; 3. Anti-epileptic effect, which can block pathological calcium overload in nerve cells to prevent paroxysmal depolarization and cell discharge, thereby avoiding epileptic seizures; 4. Protect the myocardium and significantly reduce ischemic myocardial damage; 5. Improve renal function and can be used for chronic renal failure; 6. It also has anti-histamine effect.

More

This product is a calcium channel blocker. It can prevent cell damage caused by pathological calcium overload in cells due to ischemia and other reasons. It has the following effects: 1. Relieve vasospasm, especially for the basilar artery and internal carotid artery; 2. Vestibular inhibition, which can increase blood flow in the cochlear arterioles and improve vestibular organ circulation; 3. Anti-epileptic effect, which can block pathological calcium overload in nerve cells to prevent paroxysmal depolarization and cell discharge, thereby avoiding epileptic seizures; 4. Protect the myocardium and significantly reduce ischemic myocardial damage; 5. Improve renal function and can be used for chronic renal failure; 6. It also has anti-histamine effect.

30484-77-6 25
Fluocinolone acetonide cream
The main component of this product is fluocinolone acetonide. Its chemical name is: 11β-hydroxy-16α, 17-[(1-methylethylidene)-bis(oxy)]-21-(acetoxy)-6α, 9-difluoropregnane-1,4-diene-3,20-dione.
Name Description Content CAS NO. Registered Holders
Fluocinonide

This product is an adrenal cortex hormone drug. External use can shrink dermal capillaries, inhibit the proliferation or regeneration of epidermal cells, inhibit the regeneration of fibroblasts in connective tissue, stabilize intracellular lysosomal membranes, and prevent tissue damage caused by the release of lysosomal enzymes. It has strong anti-inflammatory and anti-allergic effects.

More

This product is an adrenal cortex hormone drug. External use can shrink dermal capillaries, inhibit the proliferation or regeneration of epidermal cells, inhibit the regeneration of fibroblasts in connective tissue, stabilize intracellular lysosomal membranes, and prevent tissue damage caused by the release of lysosomal enzymes. It has strong anti-inflammatory and anti-allergic effects.

356-12-7 14
Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.