Ranitidine Hydrochloride BP-USP

Ranitidine Hydrochloride BP-USP Specification

Loss on Drying
0.75%

Solubility
Very soluble in water sparingly soluble in alcohol.

Ph Level
4.5-6.0

Molecular Weight
350.87 g/mol

Storage
Dry Place

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.

Pharmaceutical Excellence from India

Manufactured and supplied in India, Ranitidine Hydrochloride BP-USP stands out for its consistent quality and adherence to stringent BP and USP standards. This pharmaceutical intermediate is preferred by leading exporters and suppliers for its verified purity and reliable shelf life, guaranteeing suitability for large-scale pharmaceutical production and compounding.

Optimal Efficacy and Safety

The high purity (97.5%-102.0%) and controlled pH range (4.5-6.0) of Ranitidine HCL ensure safe integration into medicinal products. Its molecular stability and very high solubility in water make formulation straightforward, while loss on drying is limited to 0.75%, securing product consistency over its 3-year shelf life.

FAQs of Ranitidine Hydrochloride BP-USP:

Q: How should Ranitidine Hydrochloride BP-USP be stored to maintain its stability?

A: Ranitidine Hydrochloride BP-USP should be stored in a dry place at room temperature, away from moisture and direct sunlight. Proper storage helps maintain its efficacy and stability throughout its 3-year shelf life.

Q: What are the main uses of Ranitidine Hydrochloride BP-USP in the pharmaceutical industry?

A: This compound is primarily used to formulate medications treating indigestion, heartburn, and acid reflux conditions like gastro-oesophageal reflux disease (GERD). Its rapid solubility and high purity make it an essential ingredient in oral pharmaceutical products.

Q: When is Ranitidine HCL most beneficial for patients?

A: Ranitidine HCL is most beneficial when patients experience symptoms of acid reflux, indigestion, or heartburn. It works by reducing stomach acid production, offering relieffrom discomfort and promoting better digestive health.

Q: Where is Ranitidine Hydrochloride BP-USP manufactured and supplied from?

A: This pharmaceutical intermediate is manufactured, exported, and supplied from India, meeting strict BP and USP standards for global pharmaceutical use.

Q: What is the typical process for using Ranitidine HCL in medicine production?

A: Manufacturers typically blend Ranitidine HCL, a highly soluble powder, with excipients and other necessary ingredients to create tablets, capsules, or liquid formulations designed for effective acid reduction.

Q: What are the benefits of using highly purified Ranitidine HCL powder?

A: Utilizing highly purified Ranitidine HCL ensures consistency, safety, and high efficacy in finished pharmaceutical products, reducing the risk of impurities and supporting regulatory compliance.

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