Roxatidine acetate hydrochloride is a specific, competitive histamine H2 receptor antagonist that inhibits gastric acid secretion and ulcer formation. Roxatidine acetate hydrochloride is a competitive histamine H2 receptor antagonist that upon oral absorption is rapidly converted to its active metabolite roxatidine. By inhibiting the binding of histamine to H2 receptors, roxatidine reduces both intracellular cAMP concentrations and gastric acid secretion by parietal cells.
|Appearance||White to almost white crystalline powder||White crystalline powder|
|Loss on drying||≤0.5%||0.3%|
|Residue on ignition||≤0.1%||0.07%|
|Appearance:||White to almost white crystalline powder|
|Package details:||100g/bottle; 1kg/foil bag|
It can be used for gastric ulcer, duodenal ulcer, anastomotic ulcer, Zhuo-Ehrlich syndrome, reflux esophagitis, etc.
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