At Ekang Nutra, we manufacture dietary supplements under FDA-registered, independently cGMP-certified operations at our California facility — certified by Eurofins Healthcare Assurance and accredited by ANAB under ISO/IEC 17065. Brands partnering with us get a manufacturing process built on verified compliance, not self-declared claims.
Custom Formulations
We understand every brand is unique, with distinct audiences, positioning and product goals. Whether you need custom capsule, softgel or powder formulations, turnkey private label solutions, or specialized supplement development, our experienced R&D and production team supports you from concept and formula testing through to finished, market-ready products. With in-house, cGMP-compliant manufacturing, we maintain strict quality control, reliable lead times and flexible batch sizes for both emerging and established brands.
Production Facility
Our 13,000 sq. ft. California manufacturing facility is fully equipped with professional encapsulation, powder mixing, and end-to-end packaging and labeling equipment to provide consistent, cGMP-compliant supplement manufacturing. We implement standardized operating procedures throughout every production phase to safeguard product uniformity. We cater to clients ranging from small startups to mature established brands, delivering scalable, rigorously quality-controlled production that adapts to both low minimum runs and large bulk orders.
Fast & Efficient Turnaround Time for Supplement Manufacturing
- Certifications: FDA Registered, cGMP Certified (Eurofins Healthcare Assurance, ANAB / ISO-IEC 17065), California Processed Food Registration
- Daily Production Capacity:Capsules: 2,000,000 per day; Powder: 60,000 sachets per day; Tablet packaging: 1,500,000 tablets per day; Bottle packaging: 50,000 bottles per day; Pouch/bag packaging: 100,000 pouches per day
- Turnaround Time: We know how important it is to launch on time. Once raw materials and packaging arrive at our facility, production typically completes within 4–8 weeks — without compromising on quality control at any stage.
Backed by Verified Compliance
Our California manufacturing facility operates under independently verified cGMP certification and maintains applicable federal and state registrations for dietary supplement manufacturing and packaging.
Independently cGMP Certified
Certified by Eurofins Healthcare Assurance through an independent facility audit, with certification accredited by ANAB under ISO/IEC 17065.
View cGMP Certification
FDA-Registered Facility
Our California dietary supplement manufacturing and packaging facility maintains an active FDA Food Facility Registration.
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California Processed Food Registration
Registered with the California Department of Public Health for processed food manufacturing and packing at our Chino facility.
View California RegistrationPremium Raw Ingredients
We source raw materials only from pre-audited, verified suppliers with complete qualification documentation. Every incoming lot undergoes strict, multi-layered rigorous testing before it is approved to enter our manufacturing process. We conduct full spectrum analysis to confirm ingredient safety, purity and potency. After all, a consistent finished dietary supplement product is only as reliable as the raw materials behind it, and raw material quality remains our first line of quality control.
Raw Material Tests
Identity Test — Confirming each raw material is what it claims to be
Potency Test — Verifying active ingredient levels meet specification
Microbiology Test — Screening for harmful bacteria and contaminants
Heavy Metals Test — Detecting and limiting toxic metal content
Known Allergen Test — Identifying potential allergens for consumer safet
