MEDIOCON INC offers NEM® Partially Hydrolyzed Chicken Eggshell Membrane Powder, a branded eggshell membrane ingredient derived from chicken eggshells. NEM® is a patented partially hydrolyzed eggshell membrane ingredient produced from inspected chicken eggshells using steam separation followed by a gentle enzymatic partial-hydrolysis process.
Eggshell membrane naturally contains structural proteins, including collagen, together with glycosaminoglycans such as hyaluronic acid and chondroitin sulfate. NEM® is designed as a nutritional ingredient for formulations focused on joint health and connective-tissue support.
The Food Safety and Standards Authority of India (FSSAI) lists NEM® partially hydrolyzed chicken eggshell membrane powder under application 01/Std/PA/FSSAI/2020 & 26.10.2021, with Food Category 99.7. The approved entry identifies M/s Zenova Bio Nutrition Pvt. Ltd., Hyderabad, Telangana as the applicant.
A published NEM® Certificate of Analysis specifies an off-white to tan powder, FT-IR identity conformity, minimum hyaluronic acid and sulfated glycosaminoglycan levels, minimum collagen, moisture limit and heavy-metal specifications.
MEDIOCON INC supplies NEM® Partially Hydrolyzed Chicken Eggshell Membrane Powder according to applicable product specifications, quality requirements and available documentation.
| Parameter | Specification |
|---|---|
| Appearance | Off-white to tan powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying NEM® Partially Hydrolyzed Chicken Eggshell Membrane Powder Manufacturer & Supplier in India | MEDIOCON INC and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our NEM® Partially Hydrolyzed Chicken Eggshell Membrane Powder Manufacturer & Supplier in India | MEDIOCON INC 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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