Robinson Pharma
High-volume maker of softgels, including vegetarian, plus tablets, capsules, gummies, powders and liquids.
FDA enforcement databases, inspection classifications, and warning letter archives reviewed per our Tier 4 protocol. No unresolved adverse findings identified in our review as of the vendor's review date.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Robinson Pharma operates over 1 million sq ft of manufacturing space across eight to nine facilities in Santa Ana and Costa Mesa, California. Founded in 1989, the company publishes annual capacity figures of 20 billion softgels (including vegetarian), 14 billion tablets and capsules, 7 billion gummies, and 100,000 metric tons of powder; these are company-reported, not independently audited. Robinson Pharma reports certifications from NSF, UL, and Eurofins, and carries ISO 9001:2015 and SQF credentials. As of September 2026, NSF/ANSI 455-2 (its Santa Ana facility, NSF public directory), SQF (SQFI directory) and USDA Organic (USDA Organic Integrity Database) are independently confirmed, and USP lists the company in its Dietary Supplement Verification Program. The company recently expanded with new high-speed liquid production lines and additional tablet capabilities. They serve brands that need high-volume production runs with claims of the shortest lead times in the industry. Their facility count has grown from seven to nine buildings in recent years, funded partly by a $40.7 million property acquisition.
Certifications
3 of 8 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Softgels · Gummies · Tablets · Capsules · Powders · Liquids
- SERVICES
- Secondary Packaging
- Blister Packaging
- Bottle Filling
- CAPABILITIES
- Custom formulas · Private label or white label · Packaging
- DOSAGE FORMS
- capsules · gummies · liquids · powders · softgels · tablets
Sources
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Minimum order quantities not publicly disclosed (likely high given production scale)
- Lead times claimed as 'shortest in industry' but specific timelines not published
- USP lists the company in its Dietary Supplement Verification Program, which verifies individual products; the listing does not mean every product it makes carries the USP Verified mark (USP participants page, read 2026-09-25)
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Robinson Pharma and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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