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High Purity Meloxicam API Powder
High Purity Meloxicam API Powder
High Purity Meloxicam API Powder
High Purity Meloxicam API Powder

High Purity Meloxicam API Powder

  • $60

    1-199 Others

  • $55

    200-499 Others

  • $50

    ≥500 Others

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Product Attributes

Product Description

Product Overview

Meloxicam Fever Reduction Medicine is a pharmaceutical ingredient based on meloxicam, a non-steroidal anti-inflammatory drug (NSAID) compound commonly used in regulated pharmaceutical formulations. It is primarily developed for products intended to support reduction of inflammation, pain management, and related therapeutic applications under professional medical supervision.

As a pharmaceutical active ingredient, meloxicam requires controlled quality specifications, analytical verification, and strict manufacturing standards. It is supplied as a high-purity raw material for pharmaceutical formulation development, quality testing, and regulated medicine production.

What Is Meloxicam?

Meloxicam is an oxicam-class NSAID compound belonging to the enolic acid derivative group. It is commonly formulated in pharmaceutical products because of its anti-inflammatory and analgesic properties.

Meloxicam raw material is manufactured through controlled synthesis and purification processes. Pharmaceutical manufacturers evaluate this ingredient based on identity, assay, impurity profile, stability, and compliance with applicable quality standards.

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Specifications

Item Specification
Product Name Meloxicam Pharmaceutical Raw Material
Common Name Meloxicam
Category Pharmaceutical Active Ingredient / NSAID Compound
CAS Number 71125-38-7
Molecular Formula C14H13N3O4S2
Molecular Weight 351.40 g/mol
Appearance Light yellow to yellow crystalline powder
Assay Method HPLC analysis for meloxicam content determination
Common Purity Grade Pharmaceutical-grade purity specifications according to applicable pharmacopeial or customer requirements
Solubility Practically insoluble in water; solubility depends on formulation conditions
Shelf Life Typically 24–36 months under recommended storage conditions
Storage Store in a cool, dry place protected from light and moisture
Packaging Aluminum foil bags or pharmaceutical-grade containers with customized packaging options
Applications Pharmaceutical formulation development, quality testing, and regulated medicine manufacturing

Key Features

  • Provides a pharmaceutical-grade meloxicam active ingredient for regulated applications.
  • Offers defined chemical identity and controlled analytical specifications.
  • Supports development of tablets, capsules, and other pharmaceutical dosage forms.
  • Suitable for manufacturers requiring documented API quality control.

Applications

  • Pharmaceutical Manufacturing: Used as an active pharmaceutical ingredient in approved medicine formulations.
  • Tablet Production: Suitable for development of oral solid dosage forms.
  • Capsule Formulations: Used in pharmaceutical capsule development where applicable.
  • Quality Control Testing: Used for analytical evaluation and pharmaceutical research purposes.

Meloxicam API Selection Guide

When sourcing meloxicam pharmaceutical raw material, buyers should focus on API quality documentation, assay accuracy, impurity control, stability information, and manufacturing consistency. Pharmaceutical APIs require a higher level of quality review than general chemical ingredients.

Selection Factor Buyer Consideration Application Impact
Assay Purity Confirms meloxicam content and batch consistency Important for accurate pharmaceutical formulation
Impurity Profile Evaluates related substances and process-related impurities Supports regulatory quality requirements
Documentation Includes COA, analytical methods, and technical records Supports supplier qualification and quality review

Pharmaceutical buyers should review analytical data, specification sheets, stability information, and quality documentation before selecting meloxicam raw material for manufacturing programs.

Why Choose This Product

  • Designed for pharmaceutical ingredient applications requiring controlled specifications.
  • Supports professional formulation development with analytical quality documentation.
  • Quality evaluation may include identity testing, HPLC assay, related substance analysis, residual solvent testing, heavy metals testing, and moisture determination.
  • Suitable for bulk API supply and pharmaceutical manufacturing requirements.
  • Technical documents such as COA, TDS, and SDS can support buyer quality assessment.

Packaging Options

Meloxicam pharmaceutical raw material is commonly supplied in sealed pharmaceutical-grade packaging to maintain stability during storage and transportation. Packaging formats can be customized according to handling and production requirements.

OEM & Pharmaceutical Supply

Meloxicam API can support pharmaceutical development projects, dosage form manufacturing, and regulated medicine production programs. Supply support may include documentation preparation, specification alignment, and customized packaging solutions.

Quality Control

Each batch should undergo quality evaluation including:

  • Identity confirmation
  • HPLC assay testing
  • Related substance analysis
  • Residual solvent testing
  • Heavy metals analysis
  • Moisture content testing

Conclusion

Meloxicam Pharmaceutical Raw Material provides pharmaceutical manufacturers with a controlled active ingredient featuring defined chemical properties, analytical verification, and professional quality specifications. Contact us today to request samples, a COA, technical documents, and a wholesale quotation for Meloxicam pharmaceutical raw material.

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Packaging & Delivery

Packaging & Delivery

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