Doxofylline GMP

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Product Details:

Refractive Rate Not determined
HS Code 29349900
Physical Form Powder
Shelf Life 5 years
Melting Point 221-223C
Molecular Weight 266.26 g/mol
Solubility Freely soluble in water, slightly soluble in ethanol
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Doxofylline GMP Price And Quantity

Minimum Order Quantity 100 Kilograms

Doxofylline GMP Product Specifications

Shelf Life 5 years
Physical Form Powder
Refractive Rate Not determined
HS Code 29349900
Molecular Weight 266.26 g/mol
Melting Point 221-223C
Appearance White to almost white crystalline powder
Solubility Freely soluble in water, slightly soluble in ethanol
Storage Store in a cool, dry place, protected from light
Grade Pharmaceutical Grade
Product Type Active Pharmaceutical Ingredient
Ingredients Doxofylline
Usage For manufacturing of pharmaceutical formulations
EINECS No 274-898-9
Shape Crystalline
Purity >99%
Application Used as a bronchodilator in the treatment of asthma and COPD
Smell Odorless
CAS No 69975-86-6
Properties White to almost white powder, Good flowability, Stable under recommended storage conditions
Taste Bitter
Poisonous NO
Density 1.4 Gram per cubic centimeter(g/cm3)
Structural Formula Available on request
Molecular Formula C11H14N4O4

Stability Stable under recommended conditions
Residual Solvents Within ICH limits
Microbial Limits Complies with pharmacopeial standards
Packaging Double LDPE bag in HDPE drum of 25 kg net
Loss on Drying <0.5%
Heavy Metals <10 ppm
Manufacturing Standard GMP (Good Manufacturing Practice) compliant

Doxofylline GMP Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Jump on the opportunity to elevate your pharmaceutical manufacturing with our Exclusive Doxofylline GMP-a lofty and immaculate product crafted under stringent Good Manufacturing Practices. With a splendid purity of over 99% and an appearance ranging from white to almost white crystalline powder, this product promises consistent quality. Stable under recommended storage conditions and free of harmful heavy metals (<10 ppm), our Doxofylline is ideal for producing effective bronchodilators for asthma and COPD treatment. Try Now and ensure your formulations meet impeccable standards with our robust, GMP-compliant supply from India.

Unmatched Competitive Advantage with Doxofylline GMP

Doxofylline GMP boasts splendid application versatility, primarily serving as a high-purity bronchodilator for asthma and COPD pharmaceutical formulations. Its immaculate physical properties and stability offer reliability for both general and specialized pharmaceutical use. The primary competitive advantage lies in its superior GMP compliance, ensuring safety and quality for manufacturers, distributors, and suppliers. Jump on this exclusive solution to attain seamless integration in your formulation lines, benefiting from its remarkable solubility and exceptional flowability.

FOB Port, Certifications, and Packaging Details for Doxofylline GMP

Your proposal amount is efficiently managed as Doxofylline GMP is dispatched promptly through major FOB ports in India. The handover process guarantees coherence with global regulatory standards, backed by GMP certification and stringent quality controls. Packaging is carried out meticulously: double LDPE bags sealed within robust HDPE drums, net 25 kg-securing product stability and avoiding contamination during transit. Rest assured, certification documents and detailed packing lists accompany every consignment for complete transparency and traceability.

FAQ's of Doxofylline GMP:

Q: How is Doxofylline GMP packaged and shipped to ensure product quality?

A: Doxofylline GMP is packaged in double LDPE bags placed inside sturdy 25 kg HDPE drums, ensuring stability and protection during transit. Shipments are dispatched from key Indian FOB ports, with comprehensive documentation provided to ensure quality upon handover.

Q: What are the primary applications and uses of Doxofylline GMP?

A: Doxofylline GMP is primarily used in manufacturing pharmaceutical formulations, specifically as a bronchodilator for treating asthma and COPD, owing to its purity, stability, and compliance with pharmacopeial standards.

Q: When should Doxofylline GMP be stored, and under what conditions?

A: Doxofylline GMP should be stored in a cool, dry place, protected from light, to maintain its stability. Under these recommended conditions, it maintains efficacy for up to five years.

Q: Where is Doxofylline GMP compliant and certified?

A: Doxofylline GMP adheres to GMP (Good Manufacturing Practice) requirements and complies fully with pharmacopeial microbial and heavy metal limits, making it suitable for regulated markets globally.

Q: What benefits does Doxofylline GMP offer manufacturers and traders?

A: Manufacturers and traders benefit from its splendid purity (>99%), consistency, and robust GMP compliance, facilitating reliable, safe, and high-quality pharmaceutical productions that meet international standards.

Q: How does the process of ordering and dispatching Doxofylline GMP work?

A: Once your proposal amount is finalized, Doxofylline GMP is promptly dispatched from India, with all shipment and certification documentation handed over at the FOB port for efficient and transparent processing.

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