Rupatidine Active Pharmaceutical Ingredients

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Rupatidine Active Pharmaceutical Ingredients

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MOQ : 25 Grams

Rupatidine Active Pharmaceutical Ingredients Specification

Heavy Metal (%)
0.001%

Melting Point
198-202C

Molecular Weight
427.96 g/mol

Boiling point
Not applicable (decomposes)

Storage
Store in a tightly closed container, in a dry and cool place

Shelf Life
5 years if properly stored

Smell
Odorless

Particle Size
90% below 10 m

Structural Formula
(Structural formula image typically available on request)

HS Code
29420090

Loss on Drying
0.5%

Solubility
Freely soluble in methanol; insoluble in water

Poisonous
Non-poisonous under recommended conditions

Molecular Formula
C26H26ClN3O

Color
White to off-white

Medicine Name
Rupatidine

Chemical Name
Rupatidine Fumarate

CAS No
158876-82-5

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used in the treatment of allergic rhinitis and urticaria

Purity(%)
>=99%

Appearance
White to off-white powder

Physical Form
Solid

Related Substances
Total impurities 0.2%

Regulatory Support
DMF available upon request

Assay (by HPLC)
>=99.0%

Identification
Complies as per specification (IR, HPLC)

Formulation Compatibility
Suitable for tablet and oral suspension formulations

Packing
HDPE drums with double polythene bags, or as required

Residual Solvents
Complies with ICH guidelines

Microbial Limits
Complies with pharmacopeial standards

Rupatidine Active Pharmaceutical Ingredients Trade Information

Minimum Order Quantity
25 Grams

Payment Terms
Cash in Advance (CID), Cash Against Delivery (CAD), Cash on Delivery (COD)

Supply Ability
500 Grams Per Month

Delivery Time
5-7 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

About Rupatidine Active Pharmaceutical Ingredients

Unlock illustrious quality with Rupatidine Active Pharmaceutical Ingredient (API), a trending and highly recommended solution renowned for its exceptional purity and phenomenal performance in the treatment of allergic rhinitis and urticaria. This API boasts a purity of 99%, total impurities at just 0.2%, and complies fully with ICH guidelines for residual solvents. Its robust regulatory support includes DMF availability on request, while its versatile compatibility suits both tablet and oral suspension formulations. Securely packed in HDPE drums, this pharmaceutical-grade powder meets the highest standards, making it a preferred choice for global markets.

Phenomenal Features and Multi-Use Applications of Rupatidine API

Rupatidine API features a highly refined, white to off-white powder ideal for pharmaceutical formulations. Primarily used in the manufacture of medications for allergic rhinitis and urticaria, it is designed for direct application in solid and liquid oral dosage forms. Its exceptional purity and compliance with rigorous pharmacopeial standards ensure safety for human use. This material is trusted in the industry for its versatility across various pharmaceutical preparations, supporting high-quality end products and excellent patient outcomes.

Premium Supply, Packaging and Export Market of Rupatidine API

Rupatidine API stands out in the export market due to its premium packaging and efficient delivery system. Packaged in robust HDPE drums with double polythene liners, it ensures secure goods transport while preserving product integrity. With India as a leading supplier, export volumes are consistently maintained to meet international demand. Samples are available for quality assurance, supporting confident purchasing decisions and strengthening global business relationships with reliable supply capabilities.

FAQ's of Rupatidine Active Pharmaceutical Ingredients:

Q: How is Rupatidine API typically used in pharmaceutical manufacturing?

A: Rupatidine API is primarily used in the formulation of medications for treating allergic rhinitis and urticaria. It is highly compatible with both tablet and oral suspension dosage forms, making it versatile for various pharmaceutical products.

Q: What regulatory support is available for Rupatidine API?

A: Rupatidine API offers robust regulatory assistance, including a Drug Master File (DMF) that is available upon request, ensuring compliance with global pharmaceutical requirements and simplifying the registration process.

Q: When can samples of Rupatidine API be obtained for quality testing?

A: Samples of Rupatidine API are available upon request, allowing potential buyers and pharmaceutical companies to test quality before placing larger orders, ensuring confidence in product performance.

Q: Where is Rupatidine API supplied from and what are the export markets?

A: Rupatidine API is exported from India, a key hub for high-quality pharmaceutical ingredients, and is supplied to multiple international markets due to its acclaimed reliability and compliance with global standards.

Q: What exceptional benefits does Rupatidine API offer compared to alternatives?

A: Rupatidine API is renowned for its phenomenal purity (99%), minimal impurities (0.2%), odorless nature, and outstanding formulation compatibility, making it a highly recommended choice for premium pharmaceutical manufacturing.

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