NutraPak USA
Contract manufacturer of softgels, gelcaps, caplets and tablets with in-house R&D and product analysis.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
NutraPak USA is an FDA-registered, cGMP-certified contract manufacturer based in Clifton, New Jersey. Their facility supports softgels, gelcaps, caplets, tablets, capsules, powders, and liquid packaging including blister packing and pouch filling. The company employs laboratory scientists and formulators providing in-house R&D, quality control testing, and product analysis. Quality protocols include raw materials testing, environmental monitoring, packaging QA, active ingredient assays, dissolution testing, bio-absorbability analysis, microbiological purity testing, and GMO testing. They offer turnkey private-labeling services.
Certifications
0 of 2 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Softgels · Capsules · Tablets · Powders · Liquids
- CAPABILITIES
- Custom formulas · Private label or white label · R&D or product development · Packaging · Quality control or lab testing
- DOSAGE FORMS
- capsules · liquids · powders · softgels · tablets
Sources
- NutraPak USA - Official Website(2026-03-26)
- NutraPak USA - Certifications(2026-03-26)
- ThomasNet - NJ Contract Manufacturing(2026-03-26)
- NutraPak USA Clifton facility page - ADDRESS CORRECTION 2026-08-15 (claims-b8 item 7): headquarters is 93 Entin Rd, Clifton NJ 07014, with a second facility in East Rutherford; no Carlstadt site is published. ADDRESS FIELDS ONLY - certifications, trust tier and assessment were NOT re-reviewed, so lastReviewed is deliberately unchanged.(2026-08-15)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between NutraPak USA 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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