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Ranitidine Hydrochloride BP-USP

Ranitidine Hydrochloride BP-USP
Ranitidine Hydrochloride BP-USP

Ranitidine Hydrochloride BP-USP Specification

  • Ph Level
  • 4.5-6.0
  • Molecular Weight
  • 350.87 g/mol
  • Storage
  • Dry Place
  • Loss on Drying
  • 0.75%
  • Solubility
  • Very soluble in water sparingly soluble in alcohol.
  • Molecular Formula
  • C13H22N4O3S HCl
  • Shelf Life
  • 3 Years
  • Medicine Name
  • Ranitidine HCL
  • Chemical Name
  • N - [2 - [ - 5 - [(Dimethylamino)methyl]
  • CAS No
  • 66357-59-3
  • Type
  • Pharmaceutical Intermediates
  • Grade
  • Medicine Grade
  • Usage
  • To treat indigestion & heartburn and acid reflux gastro-oesophageal reflux disease
  • Purity(%)
  • 97.5%-102.0%
  • Appearance
  • White to pale yellow crystalline practically odourless powder.
  • Physical Form
  • Powder
 

Ranitidine Hydrochloride BP-USP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

About Ranitidine Hydrochloride BP-USP

Ranitidineis a competitive and reversible inhibitor of the action of histamine, releasedby enterochromaffin-like (ECL) cells, at the histamine H2-receptors on parietalcells in the stomach, thereby inhibiting the normal and meal-stimulatedsecretion of stomach acid.

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