Ranitidine HCL IP contract manufacturing API

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Ranitidine HCL IP contract manufacturing API

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MOQ : 100 Kilograms

Ranitidine HCL IP contract manufacturing API Specification

Molecular Formula
C13H22N4O3S HCl

Solubility
Freely soluble in water, very slightly soluble in ethanol

Molecular Weight
350.87 g/mol

Smell
Odorless

Ph Level
4.5 - 6.0 (1% solution)

HS Code
29349900

Particle Size
Passes 60 mesh

Structural Formula
Available on request

Color
White to pale yellow

Boiling point
Not applicable / Decomposes

Shelf Life
5 years from the date of manufacture

Poisonous
Non-poisonous as per IP specifications

Melting Point
134-140C

Heavy Metal (%)
Not more than 20 ppm

EINECS No
266-568-5

Loss on Drying
Not more than 0.5%

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

Chloride Content
Meets IP specification

Identification
Meets IP requirements (by IR and chemical test)

Related Substances
Total impurities not more than 0.5%

Residue on Ignition
Not more than 0.1%

Certificate of Analysis (COA)
Available with every batch

Assay
99.0% to 101.0% (on dried basis)

Packing
25 kg drum with double polyethylene bags liner or as required by customer

Manufacturing Capacity
2000 kg/month

Microbial Limits
Complies with IP pharmacopeial standards

Ranitidine HCL IP contract manufacturing API Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Week

Delivery Time
7 Days

About Ranitidine HCL IP contract manufacturing API

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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