Doxofylline export quality API

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Product Details:

Ingredients Doxofylline
Smell Odorless
Shelf Life 5 years from date of manufacturing if properly stored
Product Type Active Pharmaceutical Ingredient (API)
Grade Pharmaceutical Grade
Taste Bitter
CAS No 69975-86-6
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Doxofylline export quality API Price And Quantity

Minimum Order Quantity 100 Kilograms

Doxofylline export quality API Product Specifications

Shelf Life 5 years from date of manufacturing if properly stored
Smell Odorless
Ingredients Doxofylline
Molecular Weight 266.26 g/mol
Purity >99% (By HPLC)
CAS No 69975-86-6
Grade Pharmaceutical Grade
Taste Bitter
Product Type Active Pharmaceutical Ingredient (API)
Ph Level 5.0-7.0 (1% Solution)
Density 1.45 Gram per cubic centimeter(g/cm3)
Shape Crystalline
Solubility Soluble in water, slightly soluble in ethanol
Storage Store in a tightly closed container, in a cool, dry place, away from direct sunlight
Appearance White to off-white crystalline powder
Molecular Formula C11H14N4O4
Properties White to off-white crystalline powder, non-hygroscopic, odorless, high purity
Application Pharmaceutical formulation for the treatment of asthma and COPD
Usage For formulation of oral and injectable dosage forms
HS Code 29335990
EINECS No 274-533-3
Poisonous Non-poisonous
Melting Point 212-215C
Structural Formula C11H14N4O4
Physical Form Powder

Related Substances NMT 0.5%
Loss on Drying NMT 0.5%
Packing 25 kg fiber drum with inner double polybags
Microbial Limits Total aerobic microbial count: NMT 100 cfu/g, Total yeast & mould: NMT 10 cfu/g
Identification By IR/UV & HPLC
Residual Solvents Complies with ICH Guidelines
Heavy Metals NMT 10 ppm
Regulatory Compliance USP, EP, BP

Doxofylline export quality API Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Discover our distinguished Doxofylline export quality API, crafted for pharmaceutical excellence. With a first-rate purity exceeding 99% (HPLC), this product exemplifies impeccable quality, being non-hygroscopic, odorless, and non-poisonous. Manufactured under strict regulatory standards (USP, EP, BP), it features advanced specifications-loss on drying NMT 0.5%, heavy metals NMT 10 ppm, and compliance with ICH guidelines for residual solvents. Its customizable packaging (25 kg fiber drums with double polybags) ensures freshness and safety. Ideal for asthma and COPD treatments, our Doxofylline API stands out for its white crystalline appearance and robust stability, providing consistent performance for global distributors, manufacturers, and pharmaceutical formulators.

Comprehensive Applications & Standout Features

Doxofylline export quality API is suitable for formulating both oral and injectable pharmaceutical dosage forms, specifically targeting asthma and COPD. This first-rate API is customizable, offering pharmaceutical grade quality and extra features such as high purity, advanced microbial control, and non-hygroscopic nature. Its fresh crystalline powder form is designed to enhance the safety, efficacy, and longevity of finished products. Usage versatility ensures adaptability for various pharmaceutical needs, supporting both clinical and commercial manufacturing demands.

Market Accessibility, Authoritative Certifications & Secure Transactions

Our Doxofylline API commands a strong presence in India's main domestic market, ensuring efficient goods transport and timely delivery. It is supported by internationally recognized certifications, such as USP, EP, and BP, underscoring its impeccable regulatory compliance. Multiple payment terms are available, making the outlay process smooth and reliable for distributors, suppliers, and wholesalers. Careful attention to packing and logistics guarantees product integrity from dispatch through final delivery.

FAQ's of Doxofylline export quality API:

Q: How should Doxofylline export quality API be stored for maximum shelf life?

A: Store Doxofylline API in a tightly closed container, in a cool, dry place, away from direct sunlight to ensure up to 5 years of shelf life from the manufacturing date.

Q: What benefits does Doxofylline API offer for pharmaceutical formulations?

A: The API is distinguished by its high purity (>99%), regulatory compliance, and advanced microbial limits, making it ideal for formulations treating asthma and COPD.

Q: Where can Doxofylline export quality API be used?

A: It is widely applicable in pharmaceutical formulations, especially for oral and injectable dosage forms for asthma and COPD treatments.

Q: What is the process for customizing Doxofylline API packaging?

A: Packaging can be customized upon advanced purchase to meet specific client requirements, typically offered in 25 kg fiber drums with inner double polybags for optimal freshness and safety.

Q: When can I expect delivery of Doxofylline export quality API within India?

A: Upon confirmation of the outlay and agreement, goods transport and delivery are arranged promptly, ensuring the API reaches you efficiently within the stipulated timeline.

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