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Product Description
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.
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.

| 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 |
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.
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.
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.
Each batch should undergo quality evaluation including:
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.

Packaging & Delivery
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