Palmitoylethanolamide (PEA) is a naturally occurring fatty-acid ethanolamide belonging to the N-acylethanolamine family. It is composed of palmitic acid and ethanolamine and is widely studied as a bioactive ingredient for nutraceutical and pharmaceutical applications. PEA is valued for its functional properties and suitability for incorporation into specialized formulations.
MEDIOCON INC supplies Palmitoylethanolamide with a focus on consistent quality, controlled processing and reliable raw-material sourcing. The ingredient can be supplied for nutraceutical, dietary supplement and other formulation applications according to customer requirements and applicable specifications.
Palmitoylethanolamide is used as an ingredient in nutraceutical and dietary supplement formulations. It is commonly incorporated into capsules, tablets, powders and other specialized formulations. Its use should be based on the applicable regulatory requirements and intended formulation.
Palmitoylethanolamide is a high-value bioactive lipid ingredient with good formulation versatility. It is available in powder form and can be used in various nutraceutical applications where controlled purity and consistent quality are required.
Store in a cool, dry and well-ventilated area in tightly closed packaging. Protect from moisture, excessive heat, direct sunlight and contamination. Follow the recommended storage conditions specified in the product documentation.
| Parameter | Specification |
|---|---|
| Appearance | White to off-white powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Palmitoylethanolamide Manufacturer and Supplier in India (CAS 544-31-0) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Palmitoylethanolamide Manufacturer and Supplier in India is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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