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Custom Tablet Supplement Manufacturing

Turn your formula into a finished supplement tablet. Botanovance reviews ingredients, compression feasibility and quality requirements, then coordinates samples and production through our OEM/ODM manufacturing partner. Your formula, tablet specification and packaging are agreed before you place an order.

Tablet Specifications Built Around Your Formula

Your dose, ingredient properties and excipients decide whether a formula fits your target tablet size and performance. Define these points in your brief to speed up feasibility review and quotation.
Production staff in protective clothing reviewing documents inside an ingredient manufacturing facility
Specification What to define
Formula Ingredient identities, grades and amount per serving
Serving size Tablets per serving and active content per tablet
Size and shape Preferred shape, dimensions and total tablet weight
Excipients Permitted formulation aids and ingredients to exclude
Format and finish Standard, coated, chewable or effervescent, plus appearance
Packaging Bulk or retail packs, count per pack and moisture protection
Target market Destination country, required certifications and ingredient restrictions

Total tablet weight includes excipients and any coating

A high-dose formula may need a larger tablet or more than one tablet per serving. Available sizes, tooling and finishes are confirmed during feasibility review.

Compression Feasibility and Production Planning

Production staff in protective clothing reviewing documents inside an ingredient manufacturing facility
Not every powder blend compresses well. We assess particle size, bulk density and flowability to judge whether the blend suits direct compression or needs granulated ingredients. Trial compression then checks hardness, disintegration and defects such as capping, chipping and sticking.
Our OEM/ODM manufacturing partner reports annual production of 140 million tablets. Production slots and batch sizes are confirmed for each order.
Tablet projects follow four stages:
  • Brief review: Confirm formula, tablet targets, target market and quantity.
  • Feasibility and samples: Review processing needs and arrange available sample evaluation.
  • Production planning: Confirm trial batches where needed, MOQ and scheduling.
  • Release and delivery: Complete agreed batch testing, issue release records and arrange shipment.
Need help designing the formula first? See our supplement formulation services.

Tablet Quality Checks and Batch Documentation

Agree on test methods, acceptance criteria and documentation before production. Hardness and disintegration measure different properties, and neither alone confirms overall product quality.
Production staff in protective clothing reviewing documents inside an ingredient manufacturing facility
Quality area Requirements to review
Composition Ingredient identity, active-content targets and assay methods
Physical properties Appearance, weight variation, dimensions, hardness and friability
Performance Disintegration and dissolution where applicable, such as USP <2040> for US dietary supplements
Contaminants Microbiological limits and chemical limits such as heavy metals
Storage and packaging Protective packaging, storage conditions and shelf-life data
Batch documentation COA, lot identification and release records
Testing scope and certification coverage are confirmed for the selected product and manufacturing site. See analytical testing and quality control, or request available records from our technical documents library.

MOQ, Pricing and Lead Time

Production staff in protective clothing reviewing documents inside an ingredient manufacturing facility
Tablet contract manufacturing is quoted against the agreed formula, process and packaging.
  • MOQ: Set in total tablets and, for retail packs, finished units.
  • Pricing: Driven by ingredient grade and dose, development work, tooling, processing, testing and packaging.
  • Lead time: Depends on sample approval, material availability, production scheduling and release testing. Shipping is confirmed separately.
Send your initial quantity, forecast volume and target delivery date to receive a project-specific proposal.

Tablet Manufacturing FAQs

Production staff in protective clothing reviewing documents inside an ingredient manufacturing facility

Send the formula with ingredient grades, serving size, preferred tablet format, packaging, target market and quantity. Specifications for an existing product also help.

Yes. Share the composition, ingredient grades and current specifications for feasibility review. Any changes needed for compression are agreed before production.

Not always directly. Compression may need different ingredient grades or excipients, and tablet size, hardness and disintegration are checked against the target specification. For capsules instead, see capsule manufacturing.

It depends on the blend. Excipients often support flow, compression, hardness or disintegration. List any ingredients to exclude in your brief so their impact can be assessed.

State the format you need in your inquiry. Coating and specialty formats are confirmed before quotation or sample development.

Yes. Formula availability, packaging and branding requirements are reviewed for each project. See private label supplements for the full service scope.