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Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API
Ranitidine HCL IP contract manufacturing API

Ranitidine HCL IP contract manufacturing API

Price 1400 INR/ Kilograms

MOQ : 100 Kilograms

Ranitidine HCL IP contract manufacturing API Specification

  • Melting Point
  • 134-140C
  • Poisonous
  • Non-poisonous as per IP specifications
  • Shelf Life
  • 5 years from the date of manufacture
  • Smell
  • Odorless
  • Molecular Formula
  • C13H22N4O3S HCl
  • EINECS No
  • 266-568-5
  • HS Code
  • 29349900
  • Ph Level
  • 4.5 - 6.0 (1% solution)
  • Color
  • White to pale yellow
  • Molecular Weight
  • 350.87 g/mol
  • Particle Size
  • Passes 60 mesh
  • Boiling point
  • Not applicable / Decomposes
  • Structural Formula
  • Available on request
  • Heavy Metal (%)
  • Not more than 20 ppm
  • Loss on Drying
  • Not more than 0.5%
  • Solubility
  • Freely soluble in water, very slightly soluble in ethanol
  • Storage
  • Store in a cool, dry, and well-ventilated place, protected from light and moisture
  • 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
  • 66357-59-3
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used for the treatment of ulcers, gastroesophageal reflux disease, and conditions where reduction of stomach acid is required
  • Purity(%)
  • 99% Min
  • Appearance
  • White or almost white crystalline powder
  • Physical Form
  • Powder
  • Packing
  • 25 kg drum with double polyethylene bags liner or as required by customer
  • Assay
  • 99.0% to 101.0% (on dried basis)
  • Manufacturing Capacity
  • 2000 kg/month
  • Certificate of Analysis (COA)
  • Available with every batch
  • Microbial Limits
  • Complies with IP pharmacopeial standards
  • Chloride Content
  • Meets IP specification
  • Residue on Ignition
  • Not more than 0.1%
  • Identification
  • Meets IP requirements (by IR and chemical test)
  • Related Substances
  • Total impurities not more than 0.5%
 

Ranitidine HCL IP contract manufacturing API Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • FOB Port
  • mudara
  • Payment Terms
  • Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Week
  • Delivery Time
  • 7 Days
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India, South India, Central India, West India, North India, East India, Gujarat, Karnataka, Kerala, Lakshadweep, Mizoram, Meghalaya, Manipur, Andhra Pradesh, Bihar, Chandigarh, Daman and Diu, Goa, Jharkhand, Odisha
 

Ranitidine HCL IP contract manufacturing API About



Unlock prodigious value with our peerless Ranitidine HCL IP contract manufacturing API-crafted for the most demanding pharmaceutical applications. With an assay purity of 99.0% to 101.0% (on dried basis) and Crackerjack identification by both IR and chemical tests, this pharmaceutical-grade API is in ephemeral, limited stock at the lowest price. Delivered with a COA for every batch, it surpasses IP standards for residue on ignition, related substances, and microbial limits. Odorless, non-poisonous, and with a 5-year shelf life, it's securely packed in 25 kg drums, ensuring uncompromised quality from India's leading suppliers, exporters, and exporters.

Versatile Application Surfaces and Areas

Ranitidine HCL IP contract manufacturing API is expertly tailored for use across a range of medicinal surfaces and pharmaceutical applications. Its core area of application focuses on treatments related to ulcers and gastroesophageal reflux disease (GERD), making it highly suitable for formulation in tablet and liquid forms. Designed to meet pharmaceutical industry requirements, this API serves hospitals, clinics, research centers, and contract manufacturing organizations with quality assurance at every step.


Packing, Supply Ability, and Delivery Efficiency

Every batch of Ranitidine HCL IP API is securely packed & dispatched in 25 kg drums with double polyethylene bag liners or as required by the customer. With a manufacturing and supply ability of 2,000 kg/month, we ensure prompt dispatch upon confirmation of your asking price. Orders are processed quickly and typically dispatched within industry-stipulated delivery timelines, offering reliability for distributors, wholesalers, and service providers nationwide.


FAQ's of Ranitidine HCL IP contract manufacturing API:


Q: How is the Ranitidine HCL IP API shipped and packaged for safety and quality?

A: Our Ranitidine HCL IP API is packed in 25 kg drums with double polyethylene bag liners or customized as required. Each batch is securely sealed to maintain integrity during transit and meets all industry safety and quality standards.

Q: What is the process for ordering bulk Ranitidine HCL IP API from your company?

A: To order, simply contact us with your quantity, desired packing option, and delivery location. Based on your asking price, we will confirm availability and arrange prompt packing and dispatch in line with your specifications.

Q: Where can Ranitidine HCL IP API be effectively used?

A: Ranitidine HCL IP API is ideal for use in pharmaceutical manufacturing, especially for treatments targeting ulcers, GERD, and other acid-related conditions. It is suitable for tablets, syrups, and other drug formulations.

Q: When will I receive the Certificate of Analysis (COA) for my batch?

A: A comprehensive Certificate of Analysis (COA) is provided with every batch of Ranitidine HCL IP API, ensuring compliance with all critical pharmacopeial standards and specifications upon dispatch.

Q: What are the benefits of choosing your Ranitidine HCL IP API for contract manufacturing?

A: Choosing our Ranitidine HCL IP means partnering with a supplier who offers high purity, limited stock, lowest possible pricing, reliable delivery, and robust documentation, ideal for pharmaceutical manufacturers and contract development projects.

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