Amerilab Technologies Inc.
Manufacturer focused on effervescent tablets and powders, with custom formulation and packaging.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Amerilab Technologies builds its business around effervescent tablets and powders. Based in Minnesota, it holds an NSF/ANSI 455-2 listing confirming powder and tablet scope under the dietary-supplement GMP standard. Services include custom formulation, quality operations, and packaging. For a brand developing a fizzy drink tablet or a flavored powder, the effervescent focus is the draw.
Certifications
1 of 1 certification independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Effervescent · Powders · Tablets
- CAPABILITIES
- Custom formulas · Packaging · Quality control or lab testing
- DOSAGE FORMS
- effervescent · powders · tablets
Sources
- Vendor primary site(2026-05-27)
- Cert directory cross-check(2026-05-27)
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 Amerilab Technologies 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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