Doxofylline WHO GMP

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Product Details:

Purity 99%
Appearance White crystalline powder
CAS No 69975-86-6
Taste Slightly bitter
Shelf Life 36 months
Shape Crystalline
Properties Bronchodilator; Xanthine derivative; Non-caffeine pharmacology; Used in respiratory therapy
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Doxofylline WHO GMP Price And Quantity

Minimum Order Quantity 100 Kilograms

Doxofylline WHO GMP Product Specifications

Smell Odorless
Ph Level Neutral
Application Used in the management of asthma and chronic obstructive pulmonary disease (COPD)
Molecular Formula C11H14N4O4
Physical Form Powder
Grade Pharmaceutical Grade
Taste Slightly bitter
Shelf Life 36 months
CAS No 69975-86-6
Purity 99%
Appearance White crystalline powder
Storage Store in a cool, dry place, protected from light and moisture
Usage For formulation of tablets and syrups for respiratory indications
Properties Bronchodilator; Xanthine derivative; Non-caffeine pharmacology; Used in respiratory therapy
Shape Crystalline
HS Code 2939
Melting Point 215C - 217C
Product Type Active Pharmaceutical Ingredient
EINECS No 274-802-6
Molecular Weight 266.25 g/mol
Solubility Soluble in water, slightly soluble in ethanol
Poisonous Non-poisonous as per therapeutic use guidelines
Density 1.4 Gram per cubic centimeter(g/cm3)
Structural Formula Available on request
Ingredients Doxofylline

Related Substances Total impurities 0.5%
Packaging Type Sealed double LDPE bags in HDPE drums of 25 kg net
Standard Certification WHO GMP certified
Stability Stable at room temperature when protected from moisture
Identification Confirms by IR & HPLC
Residue on Ignition 0.1%
Microbial Limits As per IP/BP/USP
Manufacturing Compliance Complies with International Pharmacopoeia
Loss on Drying 0.5%
Therapeutic Category Respiratory drug, bronchodilator
Heavy Metals 10 ppm
End Use Pharmaceutical formulations (oral dosage forms)

Doxofylline WHO GMP Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Doxofylline WHO GMP is an acclaimed, highly recommended bronchodilator recognized for its stellar efficacy in respiratory care. This distinguished pharmaceutical-grade compound, widely accessed by professionals, is manufactured under strict WHO GMP standards and surpasses international pharmacopoeia requirements. Presented as a brilliant white crystalline powder, it boasts superior purity (99%) and stability, making it ideal for tablets and syrups. Its non-poisonous, odorless profile-combined with low impurity levels-ensures safe formulation for asthma and COPD management. Available in sealed LDPE bags within HDPE drums (25kg), it is highly suitable for distributors, exporters, and manufacturers worldwide.

Versatile Application & Distinguished Features

Doxofylline WHO GMP showcases its excellence across a wide area of respiratory applications, especially in the treatment of asthma and chronic obstructive pulmonary disease (COPD). Perfect for oral dosage forms such as tablets and syrups, this pharmaceutical-grade substance features a neutral pH, is highly soluble in water, and stable at room temperature. Its non-caffeine xanthine derivative nature and stellar safety profile make it a brilliant choice for varied therapeutic and formulation requirements.

Sample, Delivery, and Export Excellence

Samples of Doxofylline WHO GMP are accessible for evaluation with prompt quotation. The product is available for quick dispatch, ensuring rapid delivery to clients both in India and on major export markets globally. Flexible payment terms are provided, catering to distributors, wholesalers, importers, and suppliers. Our commitment to efficient logistics and comprehensive service guarantees a smooth, timely experience for buyers seeking renowned respiratory therapy ingredients.

FAQ's of Doxofylline WHO GMP:

Q: How does Doxofylline benefit patients with asthma and COPD?

A: Doxofylline acts as a bronchodilator, relaxing respiratory muscles to improve airflow and ease breathing in patients suffering from asthma and chronic obstructive pulmonary disease (COPD).

Q: What are the main applications of Doxofylline WHO GMP?

A: This product is primarily used in pharmaceutical formulations like tablets and syrups intended for respiratory therapy, particularly in the management of asthma and COPD.

Q: Where is Doxofylline WHO GMP manufactured and what certifications does it hold?

A: Doxofylline WHO GMP is manufactured in India and meets stringent WHO GMP and International Pharmacopoeia standards, ensuring high quality and compliance.

Q: How is Doxofylline WHO GMP packaged for shipment?

A: The product is securely packed in double LDPE bags contained within HDPE drums, each with a net weight of 25 kg, ensuring product integrity during transport.

Q: What process ensures the purity and compliance of Doxofylline WHO GMP?

A: Each batch is validated by IR & HPLC identification methods and tested for loss on drying, heavy metals, and impurities, guaranteeing 99% purity and compliance with IP/BP/USP microbial limits.

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