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Products> Plant Extracts> Standardized Extracts> High Purity Diclofenac Sodium Powder
High Purity Diclofenac Sodium Powder
High Purity Diclofenac Sodium Powder
High Purity Diclofenac Sodium Powder
High Purity Diclofenac Sodium Powder

High Purity Diclofenac Sodium Powder

  • $40

    1-199 Others

  • $35

    200-499 Others

  • $30

    ≥500 Others

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Product Attributes

Product Description

Product Overview

Diclofenac Sodium is a pharmaceutical-grade non-steroidal anti-inflammatory drug (NSAID) active ingredient widely used in pain relief and anti-inflammatory formulations. It is commonly supplied as a high-purity API for qualified pharmaceutical manufacturers producing tablets, capsules, topical products, and other dosage forms.

Diclofenac Sodium API is selected by pharmaceutical formulators based on assay purity, impurity profile, analytical verification, regulatory documentation, and manufacturing compatibility. Reliable quality control is essential for developing consistent finished pharmaceutical products.

What Is Diclofenac Sodium?

Diclofenac Sodium is the sodium salt form of diclofenac, a phenylacetic acid derivative belonging to the NSAID category. It is commonly used as an active pharmaceutical ingredient in prescription and over-the-counter medicines designed for pain management and inflammatory conditions.

As a pharmaceutical raw material, Diclofenac Sodium is supplied in controlled purity grades and evaluated through analytical testing to ensure identity, potency, and quality consistency for pharmaceutical production.

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Specifications

Item Specification
Product Name Diclofenac Sodium API
Category Pharmaceutical API / NSAID Active Ingredient
CAS Number 15307-79-6
Molecular Formula C14H10Cl2NNaO2
Molecular Weight 318.13 g/mol
Appearance White to slightly yellow crystalline powder
Assay Grade Typically pharmaceutical grade with high purity according to applicable quality standards
Test Method HPLC assay and pharmaceutical quality testing
Identification Conforms to standard pharmaceutical identification requirements
Solubility Slightly soluble to soluble depending on solvent conditions
Shelf Life Typically 24 months under recommended storage conditions
Storage Store in a cool, dry place, protected from moisture, heat, and direct sunlight
Packaging Common packaging includes sealed aluminum foil bags and fiber drums; customized pharmaceutical packaging available
Applications Pharmaceutical tablets, capsules, topical formulations, and other pharmaceutical dosage forms

Key Benefits

  • High-purity pharmaceutical API suitable for professional drug formulation development.
  • Consistent assay and quality profile support reliable manufacturing processes.
  • Compatible with multiple pharmaceutical dosage forms including oral and topical products.
  • Supported by analytical testing and technical documentation for quality evaluation.

Applications

Diclofenac Sodium API is widely used in pharmaceutical manufacturing where a validated NSAID active ingredient is required for finished dosage forms.

  • Tablet formulations
  • Capsule formulations
  • Topical gels and creams
  • Pharmaceutical research and development
  • Contract pharmaceutical manufacturing projects

Buyer Decision Guide: Selecting Pharmaceutical-Grade Diclofenac Sodium API

For pharmaceutical API procurement, buyers should evaluate the complete quality profile rather than focusing only on assay value. Impurity control, analytical methods, documentation, and regulatory support are important factors in supplier qualification and production consistency.

Evaluation Factor Why It Matters Buyer Consideration
Assay and Potency Ensures accurate active ingredient input during formulation Review HPLC assay results and specification limits
Impurity Profile Supports pharmaceutical quality assessment Evaluate related substances and impurity testing data
Dosage Form Compatibility Influences processing and formulation design Confirm suitability for tablets, capsules, or topical products
Documentation Package Supports incoming quality control and regulatory review Request COA, TDS, SDS, and technical quality records

Why Choose This Product

  • Produced under controlled pharmaceutical manufacturing conditions.
  • Supported by standardized analytical testing for identity, assay, and quality verification.
  • Suitable for bulk API procurement and pharmaceutical formulation projects.
  • Technical documentation supports professional quality assessment.
  • Flexible packaging options are available for different supply requirements.

OEM & Private Label Support

Diclofenac Sodium can be integrated into pharmaceutical manufacturing projects requiring API supply and dosage-form development support. OEM and contract manufacturing services may include formulation development, tablet production, Capsule Manufacturing, topical preparation, packaging, and labeling solutions.

Quality Control

Quality evaluation for Diclofenac Sodium API commonly includes:

  • Identity verification
  • HPLC assay testing
  • Related substances analysis
  • Residual solvent testing
  • Heavy metals testing
  • Microbiological testing where applicable
  • Moisture content verification

Packaging Options

Diclofenac Sodium API is commonly packed in sealed pharmaceutical-grade packaging to protect material stability during storage and transportation. Bulk packaging and customized formats can be arranged according to manufacturing requirements.

Conclusion

Diclofenac Sodium API provides pharmaceutical manufacturers with a reliable active ingredient option for pain relief and anti-inflammatory formulations. With high purity, standardized analytical testing, and professional documentation support, it is suitable for commercial pharmaceutical development. Contact us today to request samples, a COA, technical documents, and a wholesale quotation for Diclofenac Sodium API.

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Packaging & Delivery

Packaging & Delivery

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