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Tablet Manufacturing

Compressed, chewable, coated and effervescent tablets with shape, size and coating options.

Tablet Manufacturing production detail image

Format planning checklist

  • From 100,000 tablets depending on tooling and coating
  • Formula feasibility and ingredient load review
  • Flavor, color, size, appearance and serving design
  • Packaging compatibility and retail/Amazon file planning
  • COA and third-party testing scope by project
Manufacturing evidence

Process, testing and packaging scope.

These are project-planning capabilities supported by the current local production and product asset library. Final specifications are confirmed in the written quotation.

Typical manufacturing path

  1. Confirm tablet type, serving size and target dimensions
  2. Review flow, compression and excipient requirements
  3. Blend and granulate when required
  4. Compress tablets with weight and hardness checks
  5. Coat, polish or inspect according to the brief
  6. Bottle or blister pack and release agreed documents

Testing scope to confirm

  • Raw-material and supplier-document review
  • Microbiology and heavy metals by agreed scope
  • Active-content testing when specified
  • Weight, hardness, friability and disintegration checks as applicable

Review quality and testing planning

Packaging choices

  • Bottle with induction seal and optional desiccant
  • Blister card with retail carton
  • Effervescent tube after moisture-barrier review
  • Custom tooling, shape, score line, color or coating subject to review

Compare packaging routes · Review custom formulation

Procurement FAQ

What is the MOQ for custom tablets?

The current planning reference is 100,000 tablets. Tooling, tablet size, coating, formula and printed components can change the final production quantity.

Can chewable or effervescent tablets be developed?

Compressed, chewable, coated and effervescent directions can be reviewed, but taste, moisture protection, tooling and packaging must be assessed separately.

Which tablet tests may be required?

The agreed plan may include identity, microbiology, heavy metals, active content, weight, hardness, friability and disintegration depending on formula and market.

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