GMP Laboratories of America
Contract manufacturer of supplements and homeopathic drug products, offering blister card packaging.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
GMP Laboratories of America is a contract manufacturer of dietary supplements and homeopathic drug products based in Anaheim, California, operating since 1994. The company runs two facilities totaling over 100,000 square feet within the Anaheim Center for Advanced Technology. GMP Labs produces capsules, tablets, powders, liquids, and gummies, with a stated hard-shell encapsulation capacity exceeding 400 million capsules per month. USDA's Organic INTEGRITY Database confirms its organic handling certification through SCS Global Services. Its two Anaheim facilities are listed in NSF's public directory under NSF/ANSI 455-2 for dietary supplement manufacturing. GMP Labs offers services from custom formulation and R&D through manufacturing, packaging, and labeling, including Amazon FBA-compliant packaging and blister card packaging.
Certifications
2 of 4 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Capsules · Tablets · Powders · Gummies · Liquids
- SERVICES
- Amazon FBA Prep
- Secondary Packaging
- Blister Packaging
- Bottle Filling
- CAPABILITIES
- Custom formulas · Private label or white label · R&D or product development · Small runs or low minimums · Packaging · OTC or homeopathic drugs
- DOSAGE FORMS
- capsules · gummies · liquids · powders · tablets
Sources
- GMP Labs Homepage(2026-09-06)
- GMP Labs Certifications Page(2026-09-06)
- USDA Organic INTEGRITY Operation Profile(2026-09-06)
- NSF/ANSI 455-2 Facility Listings(2026-09-06)
- GMP Labs Request a Quote(2026-09-06)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- FDA Drug Establishment Registration (FEI) number not publicly disclosed; FURLS verification not possible without FEI (audit 2026-05-21)
- Specific MOQ and lead times disclosed on quote request only (audit 2026-05-21)
- FDA Drug Establishment registration number (FEI) not publicly available for independent verification
- Specific MOQ and lead times require direct quote request
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between GMP Laboratories of America 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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