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Ranitidine HCL IP
Ranitidine HCL IP

Ranitidine HCL IP

MOQ : 100 Kilograms

Ranitidine HCL IP Specification

  • Smell
  • Odorless
  • Heavy Metal (%)
  • Not more than 0.001%
  • Ph Level
  • 4.5 - 6.0 (1% solution)
  • EINECS No
  • 266-565-6
  • Shelf Life
  • 5 Years
  • Solubility
  • Soluble in water, sparingly soluble in alcohol
  • Boiling point
  • Not applicable (decomposes)
  • Poisonous
  • NO
  • Melting Point
  • 134-140C
  • Storage
  • Store in cool, dry, and well-ventilated area
  • Loss on Drying
  • Not more than 0.5%
  • HS Code
  • 29420090
  • Molecular Weight
  • 350.87 g/mol
  • Color
  • White to pale yellow
  • Molecular Formula
  • C13H22N4O3SHCl
  • Taste
  • Slightly bitter
  • Particle Size
  • 90% Passes through 60 mesh
  • Structural Formula
  • C13H22N4O3SHCl (as per label)
  • Medicine Name
  • Ranitidine HCL IP
  • Chemical Name
  • N-(2-((5-((dimethylamino)methyl)furan-2-yl)methylthio)ethyl)-N-methyl-2-nitroethene-1,1-diamine hydrochloride
  • CAS No
  • 66357-35-5
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • IP (Indian Pharmacopoeia)
  • Usage
  • Used for the treatment of ulcers and gastroesophageal reflux disease (GERD)
  • Purity(%)
  • 99% Min
  • Appearance
  • White to pale yellow crystalline powder
  • Physical Form
  • Solid
  • Identification
  • Conforms to IP standard tests
  • Related substances
  • Not more than specified in IP
  • Residue on ignition
  • Not more than 0.1%
  • Packing
  • Packed in HDPE drum with double inner liner
  • Bacterial Endotoxin
  • Complies with pharmacopeia limits
  • Moisture Content
  • Not more than 0.5%
  • Manufacturing Process
  • GMP compliant facility
  • Regulatory Status
  • Pharmacopeia standard (IP, BP, USP available)
  • Chloride content
  • As per IP limit
  • Assay (on dried basis)
  • 98.5% to 101.0%
 

Ranitidine HCL IP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Supply Ability
  • 1000 Kilograms Per Week
  • Delivery Time
  • 7 Days
 

Ranitidine HCL IP About



Highlighted for its Scarce impurities and Lavish compliance, Ranitidine HCL IP is a Renowned Active Pharmaceutical Ingredient (API) primarily Utilised for the treatment of ulcers and gastroesophageal reflux disease (GERD). Presented as a ravishing white to pale yellow crystalline powder, it boasts a purity of 99% minimum and strictly adheres to IP, BP, and USP standards. Packed in HDPE drums with double inner liners, this API guarantees robustness, safety, and extended shelf life. Utilise Offer advantages with a product crafted in a GMP compliant facility, maintaining the highest grade of pharmacopeia standards.

Comprehensive Applications and Ravishing Features of Ranitidine HCL IP

Ranitidine HCL IP is extensively used in the pharmaceutical sector for treating ulcers and GERD, thanks to its reliable potency and purity. Its scarce impurities, confirmed IP-standard compliance, and stable physical form ensure optimal efficacy for various formulations. This product stands out for its ravishingly consistent quality, slight bitter taste, and complete solubility in water, making it ideal for manufacturing a wide array of medicinal products. Utilise this offer for industry-leading results.


Delivering Excellence: Supply Capability and Export Policy

As a renowned distributor, exporter, and supplier in India, we charge competitive rates and ensure timely delivery on all orders of Ranitidine HCL IP. Our supply ability encompasses bulk quantities packed robustly for safety. Sample policies are tailored as per customer demand, often with no additional charge for initial evaluation. Main export markets include Asia, Africa, the Middle East, and beyond. Utilise our seamless service and swift dispatch for a reliable, hassle-free procurement experience.


FAQ's of Ranitidine HCL IP:


Q: How is Ranitidine HCL IP commonly used in pharmaceuticals?

A: Ranitidine HCL IP is widely utilised as an active ingredient in medications for treating ulcers and gastroesophageal reflux disease (GERD), formulated in both tablets and injectable forms.

Q: What distinguishes the quality of your Ranitidine HCL IP?

A: Our Ranitidine HCL IP conforms to stringent IP, BP, and USP standards, with lavish purity of 99% minimum, scarce related substances, and compliance to all pharmacopeial limits for impurities and contaminants.

Q: When can customers expect to receive their Ranitidine HCL IP orders?

A: Orders are processed efficiently, and deliveries are dispatched promptly, ensuring customers receive their shipments within agreed timelines, based on region and quantity ordered.

Q: Where can the product be shipped, and are there any delivery restrictions?

A: Ranitidine HCL IP can be shipped globally, including to main export markets in Asia, Africa, and the Middle East, with no regular delivery restrictions, subject to local import regulations.

Q: What is the sample policy for Ranitidine HCL IP, and are there any charges?

A: We offer flexible sample policies, commonly providing samples without charge for initial evaluations, depending on customer requirements and order potential.

Q: How should Ranitidine HCL IP be stored for best results?

A: It should be stored in a cool, dry, and well-ventilated area away from moisture and direct sunlight to preserve its efficacy and shelf life.

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