Ranitidine HCL IP WHO GMP

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Product Details:

Smell Odorless
Structural Formula (C13H22N4O3S)HCl
Solubility Freely soluble in water, slightly soluble in alcohol
Taste Slightly bitter
Shelf Life 5 years from date of manufacture
Storage Store in a cool, dry, well-ventilated place, protected from light
Particle Size 90% passes through 80 mesh
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Ranitidine HCL IP WHO GMP Price And Quantity

Minimum Order Quantity 100 Kilograms

Ranitidine HCL IP WHO GMP Product Specifications

EINECS No 265-607-7
Boiling point Not applicable (decomposes)
Molecular Weight 350.87 g/mol
CAS No 66357-35-5
Heavy Metal (%) Not more than 0.001%
Medicine Name Ranitidine HCL IP WHO GMP
HS Code 2933 59 90
Poisonous No (for pharmaceutical grade use, follows safety regulations)
Color White to off-white
Ph Level Approximately 4.5-6.0 (1% solution)
Melting Point 137-140C
Purity(%) >99%
Type Pharmaceutical Raw Material
Loss on Drying Not more than 0.5%
Physical Form Solid
Molecular Formula C13H22N4O3S.HCl
Appearance White to Pale Yellow Crystalline Powder
Chemical Name Ranitidine Hydrochloride
Storage Store in a cool, dry, well-ventilated place, protected from light
Particle Size 90% passes through 80 mesh
Shelf Life 5 years from date of manufacture
Usage Antiulcer agent, H2 receptor antagonist
Smell Odorless
Solubility Freely soluble in water, slightly soluble in alcohol
Structural Formula (C13H22N4O3S)HCl
Taste Slightly bitter
Grade IP (Indian Pharmacopoeia), WHO GMP

Related Substances Not more than 0.5%
Identification IR/UV Spectroscopy, HPLC Conforms
Packaging 25 kg / 50 kg HDPE Drum with double poly liners or as required
Bacterial Endotoxins Less than 0.5 IU/mg
Chloride Content Conforms as per IP specification
Assay (On dried basis) 98.5%-101.0%
Residual Solvents Complies with ICH/Q3C guidelines

Ranitidine HCL IP WHO GMP Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Get the best-seller Ranitidine HCL IP WHO GMP at an unbeatable price cut-offering terrific value for pharmaceutical manufacturers. This stellar antiulcer agent boasts a dominant purity of over 99%, verified by IR/UV Spectroscopy and HPLC. With related substances under 0.5%, bacterial endotoxins below 0.5 IU/mg, and compliance with all ICH/Q3C and IP safety standards, this white to pale yellow crystalline powder is the ideal pharmaceutical raw material. Packaged in secure 25 kg/50 kg HDPE drums, it's ready for consistent supply and distribution. Experience superior performance and trust in every batch!

Versatile Application and Compatibility

Ranitidine HCL IP WHO GMP is widely applied in the pharmaceutical industry as a stellar antiulcer agent and H2 receptor antagonist. Its dominant performance makes it suitable for tablet and injection formulations across hospitals, clinics, and pharmaceutical manufacturing facilities. This product is well-suited for diverse production environments requiring high standards of purity and quality, and it integrates seamlessly into various oral and injectable drug products, ensuring reliable and effective results in patient care.

Reliable Payment Terms and Fast Shipment

Our payment terms for Ranitidine HCL IP WHO GMP are designed for flexibility, supporting both advance payment and credit options based on business profile and volume. We hold all requisite certifications, including WHO GMP and IP compliance. Goods are shipped securely by express shipping across India's main domestic markets. With an efficient supply chain and robust packaging, we ensure goods transport is smooth and timely, giving customers confidence in prompt and protected delivery every time.

FAQ's of Ranitidine HCL IP WHO GMP:

Q: How is Ranitidine HCL IP WHO GMP typically used in pharmaceutical applications?

A: Ranitidine HCL IP WHO GMP serves as an antiulcer agent and H2 receptor antagonist, primarily incorporated into the formulation of oral and injectable medicines for reducing stomach acid production.

Q: What certifications and quality standards does this product meet?

A: This product is manufactured under WHO GMP conditions, conforms to Indian Pharmacopoeia (IP) specifications, and complies with ICH/Q3C guidelines for residual solvents, ensuring the highest standards of quality and safety.

Q: When can customers expect shipment after placing an order?

A: Orders are processed promptly, and with express shipping services, delivery is typically arranged within a few business days depending on location and order size.

Q: Where can Ranitidine HCL IP WHO GMP be applied?

A: It is suitable for use in pharmaceutical factories, healthcare product facilities, and medical research settings, particularly where high-purity active ingredients are essential.

Q: What is the shelf life and best storage practice for this product?

A: Ranitidine HCL IP WHO GMP has a five-year shelf life when stored in a cool, dry, and well-ventilated environment protected from light exposure.

Q: How is the product packaged for optimal safety during transport?

A: The product is securely packed in 25 kg or 50 kg HDPE drums with double poly liners, safeguarding it from moisture, contamination, and physical damage during transit.

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