Ranitidine HCL IP contract manufacturing API

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Product Details:

Molecular Weight 350.87 g/mol
Storage Store in a cool, dry, and well-ventilated place, protected from light and moisture
Ph Level 4.5 - 6.0 (1% solution)
Melting Point 134-140C
Boiling point Not applicable / Decomposes
Poisonous Non-poisonous as per IP specifications
Color White to pale yellow
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Ranitidine HCL IP contract manufacturing API Price And Quantity

Minimum Order Quantity 100 Kilograms

Ranitidine HCL IP contract manufacturing API Product Specifications

CAS No 66357-59-3
Shelf Life 5 years from the date of manufacture
Smell Odorless
HS Code 29349900
Grade Pharmaceutical Grade
Heavy Metal (%) Not more than 20 ppm
Purity(%) 99% Min
Molecular Formula C13H22N4O3S HCl
Color White to pale yellow
Structural Formula Available on request
Usage Used for the treatment of ulcers, gastroesophageal reflux disease, and conditions where reduction of stomach acid is required
Loss on Drying Not more than 0.5%
Solubility Freely soluble in water, very slightly soluble in ethanol
Particle Size Passes 60 mesh
EINECS No 266-568-5
Chemical Name N-(2-((5-((dimethylamino)methyl)furan-2-yl)methylthio)ethyl)-N-methyl-2-nitroethene-1,1-diamine hydrochloride
Molecular Weight 350.87 g/mol
Storage Store in a cool, dry, and well-ventilated place, protected from light and moisture
Type Active Pharmaceutical Ingredient (API)
Medicine Name Ranitidine HCL IP
Ph Level 4.5 - 6.0 (1% solution)
Appearance White or almost white crystalline powder
Melting Point 134-140C
Poisonous Non-poisonous as per IP specifications
Boiling point Not applicable / Decomposes
Physical Form Powder

Related Substances Total impurities not more than 0.5%
Manufacturing Capacity 2000 kg/month
Certificate of Analysis (COA) Available with every batch
Packing 25 kg drum with double polyethylene bags liner or as required by customer
Identification Meets IP requirements (by IR and chemical test)
Chloride Content Meets IP specification
Microbial Limits Complies with IP pharmacopeial standards
Assay 99.0% to 101.0% (on dried basis)
Residue on Ignition Not more than 0.1%

Ranitidine HCL IP contract manufacturing API Trade Information

Supply Ability 1000 Kilograms Per Week
Delivery Time 7 Days

Product Description

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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