

California cGMP Supplement Manufacturing for Brand Launches
Ontario facility · FDA-registered production · Six dosage lines with published MOQs
Quote in 24 hours · Samples in 2–3 weeks · Typical shelf-ready path ≈ 11 weeks





Why Choose
A U.S.-based OEM/ODM supplement manufacturer combining life science innovation, global expertise, and advanced manufacturing solutions.
U.S. Manufacturing Base
FDA-registered, cGMP-disciplined production in Ontario, California — commercial desk at Francis Street; registered plant on Milliken Ave. Documentation packs ready for retailers and marketplaces.
Clear Capacity & MOQ
Up to 92,000 capsule bottles/day and 80,000 tablet bottles/day across six dosage lines. Capsules & tablets from 200,000 units; powder from 1,000 kg; softgels typically 300,000–500,000.
Sample → First PO Path
Typical on-plan path: quote in 24h, samples in 2–3 weeks, pilot approval, then first production PO — often shelf-ready in about 11 weeks when artwork and materials stay on schedule.
Quote in 24 Hours
Share format, volume band, and timeline — we reply within 24 hours with MOQ fit, pricing direction, and a sample plan (not a placeholder reply).
“ Extensive Dosage Form
Manufacturing Options ”



“ Our Manufacturing
Capabilities ”
HiGO delivers scalable production across multiple dosage forms, ensuring quality, efficiency, and compliance for global supplement brands.




OEM & ODM Solutions
End-to-end supplement manufacturing solutions designed to help global brands develop, scale, and commercialize high-quality health products.











