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Doxofylline WHO GMP
Doxofylline WHO GMP

Doxofylline WHO GMP

Price 1 INR/ Kilograms

MOQ : 100 Kilograms

Doxofylline WHO GMP Specification

  • Molecular Formula
  • C11H14N4O4
  • Storage
  • Store in a cool, dry place, protected from light and moisture
  • Properties
  • Bronchodilator; Xanthine derivative; Non-caffeine pharmacology; Used in respiratory therapy
  • Melting Point
  • 215C - 217C
  • Solubility
  • Soluble in water, slightly soluble in ethanol
  • EINECS No
  • 274-802-6
  • Smell
  • Odorless
  • Shape
  • Crystalline
  • Structural Formula
  • Available on request
  • Taste
  • Slightly bitter
  • Usage
  • For formulation of tablets and syrups for respiratory indications
  • Purity
  • 99%
  • HS Code
  • 2939
  • Application
  • Used in the management of asthma and chronic obstructive pulmonary disease (COPD)
  • Appearance
  • White crystalline powder
  • Grade
  • Pharmaceutical Grade
  • Density
  • 1.4 Gram per cubic centimeter(g/cm3)
  • Molecular Weight
  • 266.25 g/mol
  • Ph Level
  • Neutral
  • CAS No
  • 69975-86-6
  • Physical Form
  • Powder
  • Shelf Life
  • 36 months
  • Product Type
  • Active Pharmaceutical Ingredient
  • Ingredients
  • Doxofylline
  • End Use
  • Pharmaceutical formulations (oral dosage forms)
  • Identification
  • Confirms by IR & HPLC
  • Standard Certification
  • WHO GMP certified
  • Manufacturing Compliance
  • Complies with International Pharmacopoeia
  • Loss on Drying
  • 0.5%
  • Stability
  • Stable at room temperature when protected from moisture
  • Packaging Type
  • Sealed double LDPE bags in HDPE drums of 25 kg net
  • Microbial Limits
  • As per IP/BP/USP
  • Therapeutic Category
  • Respiratory drug, bronchodilator
  • Related Substances
  • Total impurities 0.5%
  • Heavy Metals
  • 10 ppm
  • Residue on Ignition
  • 0.1%
 

Doxofylline WHO GMP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • FOB Port
  • mudara
  • Payment Terms
  • Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India, South India, Central India, West India, North India, East India, Gujarat, Karnataka, Kerala, Lakshadweep, Mizoram, Meghalaya, Manipur, Andhra Pradesh, Bihar, Chandigarh, Daman and Diu, Goa, Jharkhand, Odisha, Punjab, Assam, Delhi, Dadra and Nagar Haveli, Andaman and Nicobar Islands, Arunachal Pradesh, Chhattisgarh, Haryana, Himachal Pradesh, Jammu and Kashmir, Madhya Pradesh, Maharashtra, Nagaland, Rajasthan, Sikkim, Tamil Nadu, Telangana, Tripura
 

About Doxofylline WHO GMP



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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