Skip to content

CONTRACT MANUFACTURING

NutraStar

Farmingdale, New JerseyReviewed May 25, 2026

Contract manufacturer of capsules, tablets and powders with an in-house laboratory and logistics services.

MOQ
Not publicly disclosed
LEAD TIME
Not publicly disclosed

Overview

NutraStar is a contract supplement manufacturer operating two facilities totaling approximately 200,000 square feet, headquartered in Farmingdale, New Jersey with a second site in Chandler, Arizona. The company offers custom formulation, private-label and contract manufacturing, packaging, in-house quality assurance, an ISO/IEC 17025 accredited laboratory, and logistics services. NutraStar's stated form factors include capsules, tablets, and powders. The company self-reports FDA registration and cGMP compliance and lists a broad set of additional certifications including NSF GMP, USDA Organic, QAI Organic, Vegan, Orthodox Union Kosher, Halal, GFCO Gluten-Free, AHPA membership, and NASC preferred supplier status. USDA Organic (QAI) was subsequently registry-confirmed 2026-07-04 via the USDA Organic Integrity Database; the remaining certifications stay self-reported.

Certifications

1 of 6 certifications independently confirmed. What this means

Capabilities

PRODUCT TYPES
Capsules · Tablets · Powders
CAPABILITIES
Custom formulas · Private label or white label · Packaging · Warehousing, fulfillment or distribution · Quality control or lab testing · In-house testing lab
DOSAGE FORMS
capsules · tablets · powders

Sources

What we couldn't verify

We did not visit this company on site. See the limits that apply to every listing.

  • NSF GMP directory listing (vendor claims NSF certification; directory search did not surface a definitive match at assessment time)
  • ISO/IEC 17025 lab accreditation scope (claimed; not independently verified)
  • FDA inspection classification history
  • Facility-square-footage allocation between Farmingdale and Chandler sites
  • USDA Organic (QAI) was registry-confirmed 2026-07-04 in the USDA Organic Integrity Database (Farmingdale NJ); the remaining claims stay self-reported (no independent directory verification completed for those during this source-checked assessment)
  • NSF GMP directory match not independently verified at assessment time
  • FDA facility registration not publicly searchable; registration claim accepted on company representation

Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires

The connection map between NutraStar 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 →

Interested in NutraStar?

Tell us about your project and we'll help you determine if this manufacturer is a good fit.

Educational information only. Not legal, regulatory, or professional advice. Inventory Ready provides independent assessments based on publicly available information. See Terms for details.