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Hangzhou Conba Pharmaceutical Co., Ltd.
  • Founded in:

    2000-03-27
  • Country:

    China China
  • Address:

    No. 568, Binkang Road, Changhe Street, Binjiang District, Hangzhou City, Zhejiang Province
  • Tax NO.:

    91330108716159914E
  • Registered Funds:

    380 million yuan
  • Website:

  • Email:

Related Drugs
Glipizide extended-release capsules
The main ingredient is glipizide. Its chemical name is 5-methyl-N-[2-[4-[[[(cyclohexylamino)carboxyl]sulfonyl]phenyl]ethyl]-pyrazinecarboxamide. Its molecular formula is C21H27N5O4S21; its molecular weight is 445.54
Name Description Content CAS NO. Registered Holders
Glipizide

This product is a sulfonylurea antidiabetic drug, which is effective for most patients with type 2 diabetes. It can reduce fasting and postprandial blood sugar and reduce glycosylated hemoglobin (HbA1c) by 1%-2%. The main function of this type of drug is to stimulate the pancreatic beta cells to secrete insulin, but the prerequisite is that the pancreatic beta cells still have a certain function of synthesizing and secreting insulin. Its mechanism is to specifically bind to the sulfonylurea receptors on the beta cell membrane, thereby closing the K channel, causing changes in membrane potential, opening the Ca2 channel, and increasing the intracellular Ca2, which promotes insulin secretion. In addition, there are extra-pancreatic effects, including improving the insulin resistance of peripheral tissues (such as liver, muscle, and fat).

More

This product is a sulfonylurea antidiabetic drug, which is effective for most patients with type 2 diabetes. It can reduce fasting and postprandial blood sugar and reduce glycosylated hemoglobin (HbA1c) by 1%-2%. The main function of this type of drug is to stimulate the pancreatic beta cells to secrete insulin, but the prerequisite is that the pancreatic beta cells still have a certain function of synthesizing and secreting insulin. Its mechanism is to specifically bind to the sulfonylurea receptors on the beta cell membrane, thereby closing the K channel, causing changes in membrane potential, opening the Ca2 channel, and increasing the intracellular Ca2, which promotes insulin secretion. In addition, there are extra-pancreatic effects, including improving the insulin resistance of peripheral tissues (such as liver, muscle, and fat).

29094-61-9 27
Glipizide extended-release capsules
The main ingredient is glipizide. Its chemical name is 5-methyl-N-[2-[4-[[[(cyclohexylamino)carboxyl]sulfonyl]phenyl]ethyl]-pyrazinecarboxamide. Its molecular formula is C21H27N5O4S21; its molecular weight is 445.54
Name Description Content CAS NO. Registered Holders
Glipizide

This product is a sulfonylurea antidiabetic drug, which is effective for most patients with type 2 diabetes. It can reduce fasting and postprandial blood sugar and reduce glycosylated hemoglobin (HbA1c) by 1%-2%. The main function of this type of drug is to stimulate the pancreatic beta cells to secrete insulin, but the prerequisite is that the pancreatic beta cells still have a certain function of synthesizing and secreting insulin. Its mechanism is to specifically bind to the sulfonylurea receptors on the beta cell membrane, thereby closing the K channel, causing changes in membrane potential, opening the Ca2 channel, and increasing the intracellular Ca2, which promotes insulin secretion. In addition, there are extra-pancreatic effects, including improving the insulin resistance of peripheral tissues (such as liver, muscle, and fat).

More

This product is a sulfonylurea antidiabetic drug, which is effective for most patients with type 2 diabetes. It can reduce fasting and postprandial blood sugar and reduce glycosylated hemoglobin (HbA1c) by 1%-2%. The main function of this type of drug is to stimulate the pancreatic beta cells to secrete insulin, but the prerequisite is that the pancreatic beta cells still have a certain function of synthesizing and secreting insulin. Its mechanism is to specifically bind to the sulfonylurea receptors on the beta cell membrane, thereby closing the K channel, causing changes in membrane potential, opening the Ca2 channel, and increasing the intracellular Ca2, which promotes insulin secretion. In addition, there are extra-pancreatic effects, including improving the insulin resistance of peripheral tissues (such as liver, muscle, and fat).

29094-61-9 27
Naproxen Enteric Coated Pellets Capsules
Each tablet of this product contains 0.125 grams of naproxen, and the excipients are starch, microcrystalline cellulose, povidone K30, sodium carboxymethyl starch, and polyacrylic acid resin II.
Name Description Content CAS NO. Registered Holders
Naproxen

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects

0.125g 22204-53-1 30
Starch

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

9005-25-8 79
Microcrystalline cellulose

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

9004-34-6 89
Povidone K 30

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

0
Sodium carboxyl methylstarch

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

9063-38-1 46
Carfopol resin

This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

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Fluconazole Granules
Chemical name: 2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)-2-propanol Molecular weight: C13H12F2N6O
Name Description Content CAS NO. Registered Holders
Fluconazole

Fluconazole is a triazole broad-spectrum antifungal drug that inhibits the reproduction and growth of fungi by highly selectively inhibiting the C-14-α-demethylation of fungal cytochrome P-450 sterols, causing the accumulation of 14-α-methyl sterols in fungi. In vitro tests have shown that this product has antibacterial activity against Cryptococcus neoformans and Candida species. Oral and intravenous injection of fluconazole in animals is effective in the following animal fungal infection models: Candida species infection (including systemic candida disease in immunodeficient animals); Cryptococcus neoformans infection (including intracranial infection); Microsporum and Trichophyton infections, etc. Fluconazole is also effective against Blastomyces dermatitidis infection and Coccidioides immitis infection (including intracranial infection); and is also effective against infections caused by Histoplasma capsulatum in normal animals and immunosuppressed animals.

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Fluconazole is a triazole broad-spectrum antifungal drug that inhibits the reproduction and growth of fungi by highly selectively inhibiting the C-14-α-demethylation of fungal cytochrome P-450 sterols, causing the accumulation of 14-α-methyl sterols in fungi. In vitro tests have shown that this product has antibacterial activity against Cryptococcus neoformans and Candida species. Oral and intravenous injection of fluconazole in animals is effective in the following animal fungal infection models: Candida species infection (including systemic candida disease in immunodeficient animals); Cryptococcus neoformans infection (including intracranial infection); Microsporum and Trichophyton infections, etc. Fluconazole is also effective against Blastomyces dermatitidis infection and Coccidioides immitis infection (including intracranial infection); and is also effective against infections caused by Histoplasma capsulatum in normal animals and immunosuppressed animals.

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Finasteride Tablets
Each tablet contains 5 mg of finasteride.
Name Description Content CAS NO. Registered Holders
Finasteride

This drug belongs to the 4-nitrogen steroid hormone compound and is a specific type II 5alpha;-reductase competitive inhibitor. It inhibits the conversion of peripheral testosterone into dihydrotestosterone, reduces the level of dihydrotestosterone in the blood and tissues such as the prostate and skin, and inhibits prostate hyperplasia by reducing the level of dihydrotestosterone in the blood and prostate tissues, thereby improving the related clinical symptoms of benign prostatic hyperplasia.

More

This drug belongs to the 4-nitrogen steroid hormone compound and is a specific type II 5alpha;-reductase competitive inhibitor. It inhibits the conversion of peripheral testosterone into dihydrotestosterone, reduces the level of dihydrotestosterone in the blood and tissues such as the prostate and skin, and inhibits prostate hyperplasia by reducing the level of dihydrotestosterone in the blood and prostate tissues, thereby improving the related clinical symptoms of benign prostatic hyperplasia.

5mg 98319-26-7 50
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