US Pharmatech Inc.
OEM and private label manufacturer packaging softgels, capsules, tablets, liquids and powders.
- MOQ
- Contact for quote
- LEAD TIME
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Overview
US Pharmatech Inc. is a Las Vegas, Nevada dietary supplement OEM and private-label manufacturer with packaging capacity across softgel, capsule, tablet, liquid, powder, sachet, blister, and bottle formats. The company operates a head office in Las Vegas and a manufacturing facility in Cerritos, California, with international offices in Korea, Japan, and China.
Certifications
No certifications on record.
Capabilities
- PRODUCT TYPES
- Bottles · Sachets · Blister Packs · Softgels · Capsules · Tablets · Liquids · Powders
- CAPABILITIES
- Filling or bottling · Blister, clamshell or unit-dose packs · Stick packs or sachets · Supplement manufacturing or formulation
Sources
- US Pharmatech Official Website(2026-05-19)
- ThomasNet — US Pharmatech Inc.(2026-05-19)
- LinkedIn — US Pharmatech Inc.(2026-05-19)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- FDA Food Facility Registration number (cited as a claim on aggregator directories; not surfaced on company homepage)
- Whether NSF GMP or NSF-for-Sport applies to specific facility or scope
- Cerritos CA facility vs Las Vegas NV office scope of operations
- No certifications visible on company homepage at the 2026-05-19 review; 2026-05-19 research found FDA Food Facility Registration, NSF, Kosher, Halal, and Organic certification claims in LinkedIn and industry directory entries — these claims are noted here rather than listed as certifications because a directory or social listing alone is not enough to list a certification (registry-level verification deferred to the next review)
- Year founded not stated on company website
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between US Pharmatech Inc. 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 →
Our Evaluation Method
A full assessment applies six checks. Source-Checked listings get a lighter review.
- Independent confirmation: Claims backed by documentation, not marketing copy
- How recent the data is: Information reviewed and dated within the last 12 months
- Sources we traced: Sources cited for every key claim
- Inconsistencies flagged: Where a company's claims and public records disagree, we say so
- What we disclose: Material connections stated directly on affected listings
- What we don't know: When we can't assess something, we say so explicitly
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