Vitaquest International
Maker of capsules, powders and specialty tablets, including effervescent and orally disintegrating forms.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Vitaquest International has manufactured dietary supplements for over 40 years from four New Jersey locations listed in the NSF public directory (Parsippany, Paterson, and two in West Caldwell). The company reports being the first nutraceutical manufacturer in the United States to earn FSSC 22000 certification (self-reported). Vitaquest appears in USP's Verification Program Participants list under the GMP Audit Only Program, not under the Dietary Supplement Verification Program; a GMP Audit Only listing is not the USP Verified product mark. Vitaquest serves over 500 brands globally and produces more than 4,000 products. Their capabilities include specialty dosage forms like effervescent tablets, orally disintegrating tablets, and microencapsulated ingredients. A dedicated particle engineering facility handles complex formulations that most manufacturers cannot produce. The company employs 500 to 700 people and produces roughly 3 billion capsule doses and 2 billion tablet doses per year. Neither an MOQ floor nor a standard lead time is published today: the capsule-manufacturing page states turnaround depends on capsule type, materials, size and colour, and directs prospects to contact the company.
Certifications
1 of 8 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Capsules · Tablets · Powders · Chewables · Effervescent Tablets
- SERVICES
- Secondary Packaging
- Bottle Filling
- CAPABILITIES
- Custom formulas · Packaging · Specialty delivery formats
- DOSAGE FORMS
- capsules · chewables · effervescent · powders · tablets
Sources
- Vitaquest - Official Website(2026-03-12)
- USP Verification (Nutritional Outlook)(2026-03-12)
- Manufacturing Timeframes(2026-03-12)
- NSF International GMP Directory(2026-03-18)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Higher MOQ and longer lead times may not suit early-stage brands (audit 2026-05-21)
- Neither an MOQ floor nor a lead time is published; request both directly before planning a run
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Vitaquest International 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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